Towards clinical assessment of velopharyngeal closure using MRI: evaluation of real-time MRI sequences at 1.5 and 3 T

Objective

The objective of this study was to demonstrate soft palate MRI at 1.5 and 3 T with high temporal resolution on clinical scanners.

Methods

Six volunteers were imaged while speaking, using both four real-time steady-state free-precession (SSFP) sequences at 3 T and four balanced SSFP (bSSFP) at 1.5 T. Temporal resolution was 9–20 frames s⁻¹ (fps), spatial resolution 1.6×1.6×10.0–2.7×2.7×10.0 mm³. Simultaneous audio was recorded. Signal-to-noise ratio (SNR), palate thickness and image quality score (1–4, non-diagnostic–excellent) were evaluated.

Results

SNR was higher at 3 T than 1.5 T in the relaxed palate (nasal breathing position) and reduced in the elevated palate at 3 T, but not 1.5 T. Image quality was not significantly different between field strengths or sequences (p=NS). At 3 T, 40% acquisitions scored 2 and 56% scored 3. Most 1.5 T acquisitions scored 1 (19%) or 4 (46%). Image quality was more dependent on subject or field than sequence. SNR in static images was highest with 1.9×1.9×10.0 mm³ resolution (10 fps) and measured palate thickness was similar (p=NS) to that at the highest resolution (1.6×1.6×10.0 mm³). SNR in intensity–time plots through the soft palate was highest with 2.7×2.7×10.0 mm³ resolution (20 fps).

Conclusions

At 3 T, SSFP images are of a reliable quality, but 1.5 T bSSFP images are often better. For geometric measurements, temporal should be traded for spatial resolution (1.9×1.9×10.0 mm³, 10 fps). For assessment of motion, temporal should be prioritised over spatial resolution (2.7×2.7×10.0 mm³, 20 fps).

Advances in knowledge

Diagnostic quality real-time soft palate MRI is possible using clinical scanners and optimised protocols have been developed. 3 T SSFP imaging is reliable, but 1.5 T bSSFP often produces better images.Approximately 450 babies born in the UK every year have an orofacial cleft [1], the majority of which include the palate [2]. While a cleft palate is commonly repaired surgically at around 6 months [3], residual velopharyngeal insufficiencies require follow-up surgery in 15–50% of cases [4]. This residual defect results in an incomplete closure of the velopharyngeal port, which in turns leads to hypernasal speech. Assessment of velopharyngeal closure in speech therapy is commonly performed using X-ray videofluoroscopy or nasendoscopy [5,6]. While nasendoscopy is only minimally invasive, it may be uncomfortable and provides only an en face view of the velopharyngeal port. In contrast, X-ray videofluoroscopy is non-invasive and produces an image which is a projection of the target anatomy. Additional information may be obtained from projections at multiple angles [5,7], but anatomical structures may overlie each other. Furthermore, soft tissue contrast, such as that from the soft palate, is poor, although it may be improved using a barium contrast agent coating [8] at the expense of making the procedure more invasive and unpleasant. Arguably the greatest drawback of X-ray videofluoroscopy is the associated ionising radiation dose, which carries increased risk in paediatric patients [9].An increasing number of research studies have used MRI to image the soft palate [10-13] and upper vocal tract [14-17]. In contrast to X-ray videofluoroscopy and nasendoscopy, MRI provides tomographic images in any plane with flexible tissue contrast. As a result, MRI has been used to obtain images of the musculature of the palate at rest and during sustained phonation [10,18,19]. It has also been used to image the whole vocal tract at rest or during sustained phonation [20-27] and with a single mid-sagittal image dynamically during speech [13,15-17,28-35].For assessment of velopharyngeal closure, dynamic imaging with sufficient temporal resolution and simultaneous audio recording is required. Audio recording during imaging is complicated by the loud noise of the MRI scanner, and both the safety risk and image degradation caused by using an electronic microphone within the magnet. As a result, optical fibre-based equipment with noise cancellation algorithms must be used [36].In order to fully resolve soft palate motion, Narayanan et al [30] suggested that a minimum temporal resolution of 20 frames s⁻¹ (fps) is required. A similar conclusion was reached by Bae et al [13], based on measurements of soft palate motion extracted from X-ray videofluoroscopy. Using segmented MRI, Inoue et al [35] demonstrated that changes in the velar position that were evident at acquired frame rates of 33 fps were not observed at 8 fps. However, MRI is traditionally seen as a slow imaging modality and achieving sufficient temporal resolution at an acceptable spatial resolution is challenging. Furthermore, as the soft palate is bordered on both sides by air, the associated changes in magnetic susceptibility at the interfaces make images prone to related artefacts.Dynamic MRI of the vocal tract has been performed using both segmented [17,33,37] and real-time acquisitions [13,15,16,28,31,38]. Segmented acquisitions [39] acquire only a fraction of the k-space data required for each image during one repetition of the test phrase and, hence, require multiple identical repetitions. While these segmented techniques permit high temporal and spatial resolutions [35], they require reproducible production of the same phrase up to 256 times [34], leading to subject fatigue. Differences between repeats of up to 95 ms in the onset of speech following a trigger have also been demonstrated [36].In contrast to segmented techniques, real-time dynamic methods permit imaging of natural speech, but require extremely rapid acquisition and often advanced reconstruction methods. The turbo spin echo (TSE) zoom technique [40] has been used to perform real-time MRI of the vocal tract [29,31] and is available as a clinical tool. The zoom technique excites a reduced field of view in the phase encode direction, hence allowing a smaller acquisition matrix and shorter scan for a constant spatial resolution. While such spin echo-based techniques are less susceptible to magnetic field inhomogeneity related signal dropout artefacts than other sequences, the frame rates achieved with these sequences are limited to 6 fps [31]. Gradient echo-based techniques have also been used to achieve similar temporal resolution [12,41,42] in the upper vocal tract, but are often used at much higher frame rates in other MRI applications such as cardiac imaging [43,44]. A number of gradient echo sequence variants exist. Fast low-angle shot (FLASH) type sequences [45] spoil any remaining transverse magnetisation at the end of every sequence repetition (TR). In contrast, steady-state free-precession (SSFP) sequences are not spoiled [46] and the remaining transverse magnetisation is used in the next TR to improve the signal-to-noise ratio (SNR), but renders the images sensitive to signal loss in the presence of motion. Balanced SSFP (bSSFP) sequences include additional gradients to bring the transverse magnetisation completely back into phase at the end of every TR [47,48]. The result is that bSSFP sequences have high SNR and are less sensitive to motion than SSFP sequences, but are more sensitive to field inhomogeneities, which cause bands of signal dropout.Both TSE and the gradient echo techniques discussed here sample in a rectilinear or Cartesian fashion, where one line of k-space is sampled in each echo. However, for real-time speech imaging, the highest acquired frame rates have been achieved by sampling k-space along a spiral trajectory [15,16,30,49]. While spiral imaging is an efficient way to sample k-space and is motion-resilient, it is prone to artefacts, particularly blurring caused by magnetic field inhomogeneities and off-resonance protons (i.e. fat) [50]. Recently, one group successfully used spiral imaging with multiple saturation bands and an alternating echo time (TE) to achieve an acquired real-time frame rate of 22 fps [13,16]. The saturation bands were used to allow a small field of view to be imaged without aliasing artefacts. The alternating TE was used to generate dynamic field maps which were incorporated into the reconstruction to compensate for magnetic field inhomogeneities. However, such advanced acquisition and reconstruction techniques are only available in a small number of research centres.The aim of this work is to optimise and demonstrate high-temporal-resolution real-time sequences available on routine clinical MRI scanners for assessment of soft palate motion and velopharyngeal closure. Consequently, radial and spiral acquisitions were excluded and the work focuses on Cartesian gradient echo sequences with parallel imaging techniques. As more clinical MRI departments now have 3 T scanners, imaging was performed at both 1.5 and 3 T to enable comparisons. At each field strength, we optimised sequences and implemented four combinations of spatial and temporal resolution in six subjects with simultaneous audio recordings.     

Combining diffusion-weighted MRI with Gd-EOB-DTPA-enhanced MRI improves the detection of colorectal liver metastases

Objectives

To compare the diagnostic accuracy of gadolinium-ethoxybenzyl-diethylenetriaminepentaacetic acid (Gd-EOB-DTPA)-enhanced MRI, diffusion-weighted MRI (DW-MRI) and a combination of both techniques for the detection of colorectal hepatic metastases.

Methods

72 patients with suspected colorectal liver metastases underwent Gd-EOB-DTPA MRI and DW-MRI. Images were retrospectively reviewed with unenhanced T₁ and T₂ weighted images as Gd-EOB-DTPA image set, DW-MRI image set and combined image set by two independent radiologists. Each lesion detected was scored for size, location and likelihood of metastasis, and compared with surgery and follow-up imaging. Diagnostic accuracy was compared using receiver operating characteristics and interobserver agreement by kappa statistics.

Results

417 lesions (310 metastases, 107 benign) were found in 72 patients. For both readers, diagnostic accuracy using the combined image set was higher [area under the curve (Az) = 0.96, 0.97] than Gd-EOB-DTPA image set (Az = 0.86, 0.89) or DW-MRI image set (Az = 0.93, 0.92). Using combined image set improved identification of liver metastases compared with Gd-EOB-DTPA image set (p<0.001) or DW-MRI image set (p<0.001). There was very good interobserver agreement for lesion classification (κ = 0.81–0.88).

Conclusions

Combining DW-MRI with Gd-EOB-DTPA-enhanced T₁ weighted MRI significantly improved the detection of colorectal liver metastases.In patients with colorectal cancer, accurate assessment of the size, location and segmental distribution of liver metastases on a per-lesion basis is critical for treatment planning [1]. Accurate depiction of the size and distribution of liver metastases helps the selection of patients to undergo radical surgery [2,3] or minimally invasive therapy, such as radiofrequency ablation (RFA) [4], chemo-embolisation or radio-embolisation [5].The image contrast in diffusion-weighted MRI (DW-MRI) is based on differences in the mobility of water between tissues [6]. In tumour tissues, such as liver metastases, water mobility is often more impeded compared with normal parenchyma. Hence, metastases appear to have high signal intensity on DW-MRI, facilitating their detection.Compared with conventional T₂ weighted imaging, DW-MRI has been found to be superior for lesion detection in the liver [7-9]. When compared with contrast-enhanced MRI, DW-MRI had a higher diagnostic accuracy compared with superparamagnetic iron oxide (SPIO)-enhanced MRI [10] and similar diagnostic accuracy compared with gadolinium contrast-enhanced imaging [11] for detecting colorectal liver metastases. DW-MRI has also been found to be more sensitive than fluorodeoxyglucose (¹⁸FDG) positron emission tomography (PET) CT [12] for the same clinical indication. In another study, combining DW-MRI with T₁ weighted imaging after liver-specific contrast medium mangafodipir trisodium (MnDPDP) administration improved the diagnostic accuracy of colorectal liver metastases detection compared with either technique alone [13].Gadolinium-ethoxybenzyl-diethylenetriaminepentaacetic acid (Gd-EOB-DTPA; Eovist or Primovist; Bayer Schering Pharma, Berlin, Germany) is a relatively new hepatocyte-selective MR contrast medium that has been shown to be useful detecting liver metastases measuring <1 cm in diameter [14,15]. Delayed T₁ weighted imaging in the hepatocellular phase of contrast enhancement at 20 min to several hours after contrast administration demonstrates metastases as T₁ hypointense lesions against the avidly enhancing liver parenchyma.Both DW-MRI and Gd-EOB-DTPA-enhanced MRI are useful for the detection of liver metastases [7,8,14-16]. One study performed at 3 T compared the diagnostic performance of the two techniques for the identification of small (<2 cm) liver metastases [17]. Another study at 1.5 T independently compared the diagnostic performance of DW-MRI, dynamic phase MRI and hepatobiliary phase Gd-EOB-DTPA-enhanced MRI [18]. However, the possible incremental value of combining DW-MRI with Gd-EOB-DTPA-enhanced MRI for detecting colorectal metastases has not been reported. Hence, the aim of this study was to compare the diagnostic accuracy of Gd-EOB-DTPA-enhanced MRI, DW-MRI and a combination of both techniques for the detection of colorectal hepatic metastases.     

Primary vaginal cancer: role of MRI in diagnosis,staging and treatment

Primary carcinoma of the vagina is rare, accounting for 1–3% of all gynaecological malignancies. MRI has an increasing role in diagnosis, staging, treatment and assessment of complications in gynaecologic malignancy. In this review, we illustrate the utility of MRI in patients with primary vaginal cancer and highlight key aspects of staging, treatment, recurrence and complications.The incidence of primary vaginal cancer increases with age, with approximately 50% of patients presenting at age greater than 70 years and 20% greater than 80 years.¹ Around 2890 patients are currently diagnosed with vaginal carcinoma in the USA each year, and almost 30% die of the disease.² The precursor for vaginal cancer, vaginal intraepithelial neoplasia (VAIN) and invasive vaginal cancer is strongly associated with human papillomavirus (HPV) infection (93%).^3,4 In situ and invasive vaginal cancer share many of the same risk factors as cervical cancer, such as tobacco use, younger age at coitarche, HPV and multiple sexual partners.^5–7 In fact, higher rates of vaginal cancer are observed in patients with a previous diagnosis of cervical cancer or cervical intraepithelial neoplasia.^7,8As is true for other gynaecologic malignancies, vaginal cancer diagnosis and staging rely primarily on clinical evaluation by the International Federation of Gynecology and Obstetrics (FIGO).⁹ Pelvic examination continues to be the most important tool for evaluating local extent of disease, but this method alone is limited in its ability to detect lymphadenopathy and the extent of tumour infiltration. Hence, FIGO encourages the use of imaging. Fluorine-18 fludeoxyglucose-positron emission tomography (¹⁸F-FDG-PET), a standard imaging tool for staging and follow-up in cervical cancer, can also be used for vaginal tumours, with improved sensitivity for nodal involvement compared to CT alone.¹⁰ In addition to staging for nodal and distant disease, CT [simulation with three dimensional (3D) conformations] is particularly useful for treatment planning and delivery of external beam radiation. MRI, with its excellent soft tissue resolution, is commonly used in gynaecologic malignancies and has been shown to be accurate in diagnosis, local staging and spread of disease in vaginal cancer.^11,12 While no formal studies are available for vaginal cancer, in cervical cancer MRI actually alters the stage in almost 30% of patients.^13–15Treatment planning in primary vaginal cancer is complex and requires a detailed understanding of the extent of disease. Because vaginal cancer is rare, treatment plans remain less well defined, often individualized and extrapolated from institutional experience and outcomes in cervical cancer.^1,16–19 There is an increasing trend towards organ preservation and treatment strategies based on combined external beam radiation and brachytherapy, often with concurrent chemotherapy,^14,20,21 surgery being reserved for those with in situ or very early-stage disease.²² Increasing utilization of MR may provide superior delineation of tumour volume, both for initial staging and follow-up, to allow for better treatment planning.²³     

MRI features of serous oligocystic adenoma of the pancreas: differentiation from mucinous cystic neoplasm of the pancreas

Objectives

The purpose of this study was to describe the MRI features of the benign pancreatic neoplasm serous oligocystic adenoma (SOA) that differ from those of mucinous cystic neoplasm (MCN), a neoplasm with the potential for malignant degeneration.

Methods

Seven patients with SOA (seven women; mean age 36.6 years) and eight patients with MCN (eight women: mean age 39.9 years) were included. Several imaging features were reviewed: mass size, location, shape, wall thickness, cyst configuration (Type I, unilocular; Type II, multiple clustered cyst; Type III, cyst with internal septation) and signal intensity of the lesion with heterogeneity.

Results

SOA lesions were smaller (3.4 cm) than those of MCN (9.3 cm) (p=0.023). The commonest lesion shape was lobulated (85.7%) for SOA, but oval (50.0%) or lobulated (37.5%) for MCN (p=0.015). The most common cyst configuration was Type II (85.7%) for SOA and Type III (75.0%) for MCN (p=0.008). Heterogeneity of each locule in T₁ weighted images was visible in all cases of MCN, but in no case for SOA (p=0.004).

Conclusion

SOA could be differentiated from MCN by identifying the imaging features of lobulated contour with multiple clustered cyst configurations and homogeneity of each locule in T₁ weighted MR images.Serous oligocystic adenoma (SOA) is a recently described rare, benign pancreatic neoplasm and a morphological variant of serous microcystic adenoma, because it contains six or fewer cysts and the cysts are large (>2 cm) [1,2]. Pathologically, SOA is a benign pancreatic neoplasm composed of a few relatively large cysts uniformly lined with glycogen-rich cuboidal epithelial cells [3]. According to the World Health Organization classification, SOA is a subgroup of pancreatic serous cystic tumours and the term SOA is a synonym for macrocystic serous cystadenoma [3,4].The CT and MRI features of SOA of the pancreas are documented [2]. On CT and MRI, SOA typically appears as a small unilocular or bilocular cyst (<5 cm) with a thin wall (<2 mm) that lacks mural nodules or calcifications [2]. Because the cystic spaces are >2 cm, SOA images can be mistaken for mucinous cystic neoplasm (MCN), pseudocyst or intraductal papillary mucinous tumour [2,5-7]. It is very difficult to differentiate SOA from MCN by clinical and radiological features [2,6,8,9]. SOA does not require resection unless it causes symptoms, but MCN should be resected because of a potential for malignant degeneration [5,7,8]. Endoscopic ultrasound and cyst fluid aspiration have a role in distinguishing mucinous and serous lesions, but it is an invasive procedure with a risk of complications such as pancreatitis [10]. Therefore, it is clinically valuable to determine characteristic imaging findings that can distinguish SOA from MCN.Recently, Kim et al [6] and Cohen-Scali et al [5] described characteristic CT findings that can be used to differentiate SOA from MCN. MRI can demonstrate septa within a lesion with greater sensitivity than CT; therefore, MRI provides a better evaluation of tissue characteristics than CT [1,11]. However, few studies have described the MRI features of SOA [1,2]. The purpose of this study was to describe the differences in the MRI features of SOA and MCN in the pancreas.     

Diffusion-weighted MRI in the follow-up of chronic periaortitis

Objective:

To evaluate the usefulness of diffusion-weighted MRI (DWI) for the assessment of the intraindividual follow-up in patients with chronic periaortitis (CP) under medication.

Methods:

MRI data of 21 consecutive patients with newly diagnosed untreated disease were retrospectively examined before and after medical therapy, with a median follow-up of 16 weeks. DWI parameters [b800 signal, apparent diffusion coefficient (ADC) values] of the CP and psoas muscle were analysed together with the extent and contrast enhancement. Pre- and post-treatment laboratory inflammation markers were acquired parallel to each MR examination.

Results:

Statistically significant lower b800 signal intensities (p ≤ 0.0001) and higher ADC values (p ≤ 0.0001) were observed after medical treatment within the fibrous periaortic tissue. Extent and contrast enhancement of the CP showed also a statistically significant decrease (p ≤ 0.0001) in the follow-up examinations, while the control parameters within the psoas muscle showed no differences.

Conclusion:

DWI seems to be a useful method for the evaluation of response to treatment without contrast agents. The technique may be helpful in the assessment of disease activity to guide further therapeutic strategies.

Advances in knowledge:

DWI detects significant differences in the intraindividual follow-up of CP under medical therapy.Chronic periaortitis (CP) is a proliferating fibroinflammatory disease of the perivascular retroperitoneal space and aortic wall.^1–4 Owing to adventitial inflammation, some recent theories consider CP as a large vessel vasculitis.⁵ Clinical manifestations of CP include idiopathic retroperitoneal fibrosis, inflammatory aortic aneurysm and perianeurysmal retroperitoneal fibrosis.^2,6,7 The three manifestations with very similar histopathological characteristics are distinguished by the diameter of the abdominal aorta and concomitant ureteral affection.^1,3,7Specific clinical symptoms are caused by extrinsic compression of the ureters or retroperitoneal veins, resulting in hydronephrosis, oliguria, lower extremity oedema and deep vein thrombosis.^1,8Under medical treatment with steroids, CP has a good prognosis.⁷ Today tamoxifen is suggested as a safe and effective therapeutic alternative, and immunosuppressive drugs can be considered in patients with suboptimal responses to these drugs or multiple relapses.^9–11CT and MRI are the modalities of first choice for diagnosis and follow-up of CP.^1,7,12 The fibrotic para-aortic tissue shows significant contrast uptake in gadolinium-enhanced MRI.^12–14 Dynamic contrast-enhanced MRI was suggested for the assessment of the disease activity.^15,16 However, in cases with impaired renal function (e.g. by ureteral compression), gadolinium-independent imaging methods should be preferred owing to the potential development of a nephrogenic systemic fibrosis.¹⁷Diffusion-weighted MRI (DWI) is a non-contrast MR modality that has been successfully applied for the assessment of retroperitoneal masses, inflammatory abdominal aortic aneurysms and for the differentiation between retroperitoneal fibrosis and malignant retroperitoneal neoplasms.^18–21DWI indicates restricted diffusion of water, for example caused by a high cellularity in malignant disease or active inflammation. The apparent diffusion coefficient (ADC) is a quantitative parameter for the level of restricted diffusion, which is calculated from the signals of different diffusion gradients (b-values).²²In the context of untreated CP diffusion-weighted MRI may detect restricted inflammation as a sign of high cellularity caused by active inflammation.There are no data for the evaluation of intraindividual follow-up and the response to treatment by DWI of CP so far. Therefore, the aim of the present study was to analyse differences in DWI signals during follow-up in patients with CP before and after treatment. In addition, we sought to elucidate the potential of DWI in the therapy monitoring of CP.     

Focal nodular hyperplasia: characterisation at gadoxetic acid-enhanced MRI and diffusion-weighted MRI

Purpose:

The aim of this study was to assess the enhancement patterns of hepatic focal nodular hyperplasia (FNH) on gadoxetic acid-enhanced MRI and diffusion-weighted (DW) MRI.

Methods:

This retrospective study had institutional review board approval. Gadoxetic acid-enhanced and DW MR images were evaluated in 23 patients with 30 FNHs (26 histologically proven and 4 radiologically diagnosed). The lesion enhancement patterns of the hepatobiliary phase images were classified as heterogeneous or homogeneous signal intensity (SI), and as dominantly high/iso or low SI compared with those of adjacent liver parenchyma. Heterogeneous (any) SI lesions and homogeneous low SI lesions were categorised into the fibrosis group, whereas homogeneous high/iso SI lesions were categorised into the non-fibrosis group. Additionally, lesion SI on T₂ weighted images, DW images and apparent diffusion coefficient (ADC) values were compared between the two groups.

Results:

The lesions showed heterogeneous high/iso SI (n=16), heterogeneous low SI (n=5), homogeneous high/iso SI (n=7) or homogeneous low SI (n=2) at the hepatobiliary phase MR images. The fibrosis group lesions were more likely to show high SI on DW images and T₂ weighted images compared with those in the non-fibrosis group (p<0.05). ADC values tended to be lower in the fibrosis group than those in the non-fibrosis group without significance.

Conclusion:

FNH showed variable enhancement patterns on hepatobiliary phase images during gadoxetic acid-enhanced MRI. SI on DW and T₂ weighted images differed according to the fibrosis component contained in the lesion.

Advances in knowledge:

FNH shows a wide spectrum of imaging findings on gadoxetic acid-enhanced MRI and DW MRI.Focal nodular hyperplasia (FNH) is the second most common benign hepatic tumour after haemangioma, and most frequently occurs in females of childbearing and middle age [1]. It is considered to result from a congenital vascular disorder leading to a hyperplastic response of the surrounding liver parenchyma and is histologically characterised by normal hepatocytes with malformed bile ducts [2,3]. It is generally accepted that FNH can be managed conservatively and most cases do not require surgery because of the lack of malignancy potential and low risk of complications such as rupture or haemorrhage [4,5]. Therefore, the goal of imaging is to make a confident diagnosis and to avoid a biopsy or even surgical resection.MRI is a well-established and widely used diagnostic modality for detecting and characterising focal hepatic lesions and generally allows a confident diagnosis of typical FNH [6–8]. Findings of typical FNH on conventional gadolinium-enhanced MRI are brisk arterial enhancement, iso or slightly low signal intensity (SI) on the portal and equilibrium phase, iso or slightly low SI on T₁ weighted images, iso or slightly high SI on T₂ weighted images, a central scar showing high SI on T₂ weighted images and delayed dynamic enhancement [6–9]. However, when atypical imaging features are present, such as atypical findings of a central scar, high SI on T₁ weighted images or washout during the portal or equilibrium phase, it is not easy to distinguish FNH from other hypervascular tumours, such as hepatocellular adenomas, hypervascular metastasis or fibrolamellar hepatocellular carcinomas [6,9]. Indeed, according to a study by Bieze et al [6], characterisation of FNH and hepatocellular adenoma on standard MRI is inconclusive in 40% of lesions.Gadoxetic acid (Primovist®; Bayer-Schering Pharma, Berlin, Germany) is a new recently approved hepatobiliary gadolinium-based contrast agent. It has dual pharmacokinetic actions that combine extracellular properties for dynamic phase imaging with high hepatocyte-specific uptake and biliary excretion for delayed hepatobiliary phase imaging [10,11]. Many reports have concluded that FNHs show liver-specific enhancement and appear as iso or high SI on hepatobiliary phase imaging, and this enhancement pattern is a new additional criterion for diagnosing FNH, particularly in comparison with hepatocellular adenoma [6,10–15]. However, even though the major enhancement features of FNH are iso or high SI on hepatobiliary phase imaging, the portion of the central stellate scar or radiating fibrous septa of FNH demonstrates low SI owing to a lack of functioning hepatocytes. We postulate that the overall SI of FNH lesions during hepatobiliary phase imaging is dependent on their proportions of cellular and fibrous components.Diffusion-weighted (DW) imaging is useful for the detection and characterisation of hepatic focal lesions [16–18]. In theory, DW imaging measures the random motion of water molecules in biological tissues and reflects tissue properties, such as the size of the extracellular space, viscosity and cellularity [18–20]. According to prior hepatic fibrosis evaluations using DW imaging, lower apparent diffusion coefficient (ADC) values are observed in cirrhotic liver compared with normal liver tissue, which may be owing to restricted diffusion from extracellular fibrosis [21–25]. Despite the fact that FNH is benign, some lesions show diffusion restrictions, probably owing to their high cellularity [26–28], and fibrosis components contained in FNH lesions should influence the degree of diffusion restriction.The purpose of this study was to classify FNH lesions according to their enhancement pattern on hepatobiliary phase imaging and to assess the findings on DW and T₂ weighted imaging of the lesions with regard to those on hepatobiliary phase imaging.     

Iron overload: accuracy of in-phase and out-of-phase MRI as a quick method to evaluate liver iron load in haematological malignancies and chronic liver disease

Objectives

The purpose of this prospective study was to evaluate the accuracy of in-phase and out-of-phase imaging to assess hepatic iron concentration in patients with haematological malignancies and chronic liver disease.

Methods

MRI-based hepatic iron concentration (M-HIC, μmol g^–1) was used as a reference standard. 42 patients suspected of having iron overload and 12 control subjects underwent 1.5 T in- and out-of-phase and M-HIC liver imaging. Two methods, semi-quantitative visual grading made by two independent readers and quantitative relative signal intensity (rSI) grading from the signal intensity differences of in-phase and out-of-phase images, were used. Statistical analyses were performed using the Spearman and Kruskal–Wallis tests, receiver operator curves and κ coefficients.

Results

The correlations between M-HIC and visual gradings of Reader 1 (r=0.9534, p<0.0001) and Reader 2 (r=0.9456, p<0.0001) were higher than the correlations of the rSI method (r=0.7719, p<0.0001). There was excellent agreement between the readers (weighted κ=0.9619). Both visual grading and rSI were similar in detecting liver iron overload: rSI had 84.85% sensitivity and 100% specificity; visual grading had 85% sensitivity and 100% specificity. The differences between the grades of visual grading were significant (p<0.0001) and the method was able to distinguish different degrees of iron overload at the threshold of 151 μmol g^–1 with 100% positive predictive value and negative predictive value.

Conclusion

Detection and grading of liver iron can be performed reliably with in-phase and out-of-phase imaging. Liver fat is a potential pitfall, which limits the use of rSI.Iron overload is a clinically recognised condition with variety of aetiologies and clinical manifestations [1-4]. Liver iron concentration correlates closely with the total body iron stores [5]. The excess iron accumulates mainly in the liver and the progressive accumulation of toxic iron can lead to organ failure if untreated [2,4]. Several diseases causing iron overload, such as transfusion-dependent anaemia, haematological malignancies, thalassaemia, haemochromatosis and chronic liver disease, result in a large number of patients with a potentially treatable iron overload [1,2,4].Several quantitative MRI methods for iron overload measurement by multiple sequences have been established, such as proportional signal intensity (SI) methods and proton transverse relaxation rates (R₂, R₂*) [4,6,7]. A gradient echo liver-to-muscle SI-based algorithm [8] has been widely validated and used for quantitative liver iron measurement [8-11]. MRI-based hepatic iron concentration (M-HIC, μmol g^–1 liver dry weight) with corresponding R₂* [9] can be calculated with this method which is a directly proportional linear iron indicator, virtually independent of the fat fraction, as the echo times are taken in-phase [8,9]. This method showed a high accuracy in calibrations with the biochemical analysis of liver biopsies (3–375 μmol g^–1) of 174 patients. The mean difference of 0.8 μmol g^–1 (95% confidence interval of –6.3 to 7.9) between this method and the biochemical analysis is quite similar [8] to the intra-individual variability found in histological samples [12].The quantitative MRI methods are based on progressive SI decay, with the longer echo times due to relaxing properties of iron. Interestingly, this iron-induced effect is seen in MR images with multiple echoes [4,6-11], but also in dual-echo images, namely in-phase and out-of-phase imaging [13,14]. In-phase and out-of-phase imaging has become a routine part of liver MRI, performed initially for liver fat detection [6,13,15]. Quite recently some investigators have noticed an alternative approach of the sequence to detect liver iron overload due to the more pronounced SI decrease on in-phase images with the longer echo time [13,14]. Yet, to our knowledge, this is the first prospective study evaluating the accuracy of in-phase and out-of-phase imaging to assess hepatic iron concentration.The purpose of the study was to evaluate the capability and accuracy of dual-echo in-phase and out-of-phase imaging to assess hepatic iron concentration at 1.5 T in patients with haematological malignancies and chronic liver disease. MRI-based hepatic iron concentration (M-HIC, μmol g^–1) was used as a reference standard [8,9].     

Prognostic factors associated with a subchondral insufficiency fracture of the femoral head

Objective

The aim of this study was to identify the risk factors associated with the prognosis of a subchondral insufficiency fracture of the femoral head (SIF).

Methods

Between June 2002 and July 2009, 25 patients diagnosed with SIF were included in this study. Sequential radiographs were evaluated for the progression of collapse. Clinical profiles, including age, body mass index, follow-up period and Singh’s index, were documented. The morphological characteristics of the low-intensity band on T₁ weighted MRI were also examined with regards to four factors: band length, band thickness, the length of the weight-bearing portion and the band length ratio (defined as the proportion of the band length to the weight-bearing portion of the femoral head in the slice through the femoral head centre).

Results

Radiographically, a progression of collapse was observed in 15 of 25 (60.0%) patients. The band length in patients with progression of collapse [22.5 mm; 95% confidence interval (CI) 17.7, 27.3] was significantly larger than in patients without a progression of collapse (13.4 mm; 95% CI 7.6, 19.3; p<0.05). The band length ratio in patients with progression of collapse (59.8%; 95% CI 50.8, 68.9) was also significantly higher than in patients without a progression of collapse (40.9%; 95% CI 29.8, 52.0; p<0.05). No significant differences were present in the other values.

Conclusion

These results indicate that the band length and the band length ratio might be predictive for the progression of collapse in SIF.Subchondral insufficiency fractures of the femoral head (SIF) often occur in osteoporotic elderly patients [1-9]. Patients usually suffer from acute hip pain without any obvious antecedent trauma. Radiologically, a subchondral fracture is seen primarily in the superolateral portion of the femoral head [4,5,10]. T₁ weighted MRI reveal a very low-intensity band in the subchondral area of the femoral head, which tends to be irregular, disconnected and convex to the articular surface [2,4,5,7,9,11]. This low-intensity band in SIF was histologically proven to correspond with the fracture line and associated repair tissue [5,9]. Some cases of SIF resolve after conservative treatment [5,11-14]; other cases progress until collapse, thereby requiring surgical treatment [4-10,15]. The prognosis of SIF patients remains unclear.The current study investigated the risk factors that influence the prognosis of SIF based on the progression to collapse.     

Comparison of mammography, sonography, MRI and clinical examination in patients with locally advanced or inflammatory breast cancer who underwent neoadjuvant chemotherapy

Objectives

The purpose of this study was to determine the relative accuracies of mammography, sonography, MRI and clinical examination in predicting residual tumour size and pathological response after neoadjuvant chemotherapy for locally advanced or inflammatory breast cancer. Each prediction method was compared with the gold standard of surgical pathology.

Methods

43 patients (age range, 25–62 years; mean age, 42.7 years) with locally advanced or inflammatory breast cancer who had been treated by neoadjuvant chemotherapy were enrolled prospectively. We compared the predicted residual tumour size and the predicted response on imaging and clinical examination with residual tumour size and response on pathology. Statistical analysis was performed using weighted kappa statistics and intraclass correlation coefficients (ICC).

Results

The ICC values between predicted tumour size and pathologically determined tumour size were 0.65 for clinical examination, 0.69 for mammography, 0.78 for sonography and 0.97 for MRI. Agreement between the response predictions at mid-treatment and the responses measured by pathology had kappa values of 0.28 for clinical examination, 0.32 for mammography, 0.46 for sonography and 0.68 for MRI. Agreement between the final response predictions and the responses measured by pathology had kappa values of 0.43 for clinical examination, 0.44 for mammography, 0.50 for sonography and 0.82 for MRI.

Conclusion

Predictions of response and residual tumour size made on MRI were better correlated with the assessments of response and residual tumour size made upon pathology than were predictions made on the basis of clinical examination, mammography or sonography. Thus, the evaluation of predicted response using MRI could provide a relatively sensitive early assessment of chemotherapy efficacy.The advantages of neoadjuvant chemotherapy are multiple and it has been used widely during the past few years [1]. Its primary role is to induce tumour shrinkage and permit breast-conserving surgery, primarily in patients with advanced breast cancer [2-4]. Neoadjuvant chemotherapy allows earlier treatment of micrometastatic disease and the study of biological markers that might predict tumour response [5]. The effectiveness of chemotherapeutic agents in treating both primary breast cancer and potential metastatic disease may be enhanced by the presence of tumour neovascularity. If chemotherapy is given before surgery, while tumour vascularity remains intact, the chemotherapeutic agents may be better able to reach the tumour and thus be more effective.Neoadjuvant chemotherapy of locally advanced breast cancer (LABC) has also been shown to improve the resectability rate, offering disease-free and overall survival rates that are at least equivalent to those offered by surgery alone [6,7]. Pathological complete response (pCR) is clinically significant because it is associated with improved long-term prognosis and decreased risk of recurrence [6,8]. Decisions regarding the continuation of current regimens and the appropriate type and timing of surgery depend on the radiological and clinical assessment of residual tumour size during neoadjuvant chemotherapy [9,10]. Until now, many studies have shown that physical examinations, mammography and sonography provide suboptimal evaluations of lesion extent that do not allow accurate assessments of pathological response or residual tumour size [5^,11-13]. In the case of LABC, physical examination, mammography or sonography may be suitable for detecting the larger lesions of non-responders, but they have limited sensitivity for responders with smaller residual lesions [14,15]. For mammography, calcifications may persist or even increase in patients who respond to neoadjuvant chemotherapy [14,16,17].Many previous studies have shown that MRI is the most reliable technique for evaluating residual disease after neoadjuvant chemotherapy, although initial reports described frequent false-negatives with smaller-volume disease [18-27]. Recent studies have increased the sensitivity of MRI, with increased resolution, reduced slice thickness and lower enhancement thresholds being used to minimise the underestimation of residual disease [15^,22-27]. It is still difficult, however, to distinguish residual scarring, necrosis and fibrosis from viable residual malignancy and to predict accurate response after neoadjuvant chemotherapy, especially in responders. Few published studies have described work with patients with inflammatory breast cancer who underwent neoadjuvant chemotherapy because the incidence of this disease is very low [28,29]. The purpose of our study was to determine the relative accuracies of mammography, sonography, MRI and clinical examination in predicting residual tumour size and pathological response after neoadjuvant chemotherapy for locally advanced and inflammatory breast cancer. We compared each prediction method with the gold standard of surgical pathology.     

MRI manifestations of soft-tissue haemangiomas and accompanying reactive bone changes

Objectives

Soft tissue haemangiomas are common benign vascular lesions that can be accompanied by reactive changes in the adjacent bone structure. This study aimed to discuss the MRI features of soft-tissue haemangiomas with an emphasis on changes in bone.

Methods

The radiographic and MRI findings of 23 patients (9 males, 14 females; mean age 25 years; age range 2–46 years) with soft-tissue haemangiomas were analysed retrospectively. MR images were evaluated for location of the lesion, size, configuration, signal features, contrast patterns, proximity to adjacent bone and changes in the accompanying bone. Excisional biopsy was performed in 15 patients.

Results

Radiographs demonstrated phleboliths in 8 patients (34%) and reactive bone changes in 4 (19%). On MRI, T₁ weighted images showed that most of the lesions were isointense or isohyperintense, as compared with muscle tissue; however, on T₂ weighted images all lesions appeared as hyperintense. Following intravenous gadolinium-diethylene triamine pentaacetic acid (DTPA) administration, homogeneous enhancement was observed in 3 lesions and heterogeneous enhancement was seen in 19. No enhancement was observed in one patient. Bone atrophy adjacent to the lesion was observed in four patients.

Conclusion

MRI is the most valuable means of diagnosing deep soft-tissue haemangiomas. Bone changes can accompany deeply situated haemangiomas; in four of our patients, we found atrophy of the bone adjacent to the lesion. To our knowledge, this is the first report in the literature regarding atrophy of the bone adjacent to a lesion.Soft-tissue haemangioma, a frequently encountered benign vascular lesion, accounts for 7% of all benign soft-tissue tumours [1-5]. Such lesions can be cutaneous, subcutaneous, intramuscular or synovial [1]. Intramuscular haemangioma is rare and responsible for 0.8–1.8% of all haemangiomas [3,5,6]. Superficial haemangiomas are diagnosed easily because they cause discolorations of the skin; imaging techniques are rarely needed [1]. However, deep lesions are difficult to diagnose clinically, because they do not cause discolorations and grow slowly; imaging techniques are required to discriminate these deep haemangiomas from malignant lesions [1,2,7]. Bone changes accompanying haemangioma have been reported previously in the literature and include cortical thickening, erosion, medullary sclerosis, trabecular coarsening and hypertrophy [1,8]. Here, we present the MRI manifestations of soft-tissue haemangiomas and reactive changes to the neighbouring bones. To the best of our knowledge, this is the first report of its kind in the English literature.     

Pancreatic ductal adenocarcinoma with intratumoral cystic lesions on MRI: correlation with histopathological findings

The purpose of this study was to evaluate intratumoral cystic lesions of pancreatic ductal adenocarcinoma (PDAC) depicted on MRI, and to correlate these cystic lesions with their histopathological findings. This study included 12 patients (7 males and 5 females; mean age, 59 years) with intratumoral cystic lesions of PDAC detected on a retrospective MRI review. We reviewed the histopathological findings of the cystic lesions within PDACs and analysed the MRI findings, focusing on the appearance of the intratumoral cystic lesions, i.e. the size, number, margin and intratumoral location, and on the ancillary findings of PDAC, i.e. peripancreatic infiltration, upstream pancreatic duct dilatation and distal parenchymal atrophy. Intratumoral cystic lesions were classified as neoplastic mucin cysts (n = 7, 58%) or cystic necrosis (n = 5, 42%) according to the histopathological findings; they ranged in greatest dimension from 0.5 cm to 3.4 cm (mean, 1.7 cm). Seven patients had only one cystic lesion each, while the remaining five had multiple cystic lesions. Most of the neoplastic mucin cysts had smooth margins (n = 6, 86%) and eccentric locations (n = 6), whereas most cystic necroses had irregular margins (n = 4, 80%) and centric locations (n = 4). The most common ancillary findings of PDAC were peripancreatic infiltration, distal pancreatic atrophy and upstream pancreatic duct dilatation (92%, 75% and 58%, respectively). The intratumoral cystic lesions of PDACs on MRI were classified as either neoplastic mucin cysts with smooth margins and eccentric locations or cystic necroses with irregular margins and centric locations.Pancreatic cancer is the fifth leading cause of cancer-related death in both men and women and is responsible for 5% of all cancer-related deaths in the United States [1]. Despite the advances in surgical techniques, as well as the major improvements in chemotherapy and radiotherapy protocols, the prognosis of pancreatic ductal adenocarcinoma (PDAC) usually implies a 1-year survival rate of <20% and a 5-year survival rate of <5% [2].PDAC typically presents as an irregular solid tumour with a scirrhous character resulting from a prominent desmoplastic reaction. However, recent studies have shown that PDAC may be accompanied by cystic changes within or adjacent to the mass, and that the incidence of PDAC with cystic changes ranges from <1% to 8% [3, 4]. Radiologists should be familiar with PDACs with cystic changes as they may resemble more common cystic pancreatic lesions, such as pseudocysts, intraductal papillary mucinous neoplasms (IPMNs), solid pseudopapillary tumours and non-functioning islet cell tumours, all of which are managed differently and usually have better patient survival rates [5–7].Many studies have discussed the radiological appearance of PDAC accompanied by cystic lesions [6–11]. Most of these studies have discussed pseudocysts or retention cysts depicted adjacent to the PDAC or in the extrapancreatic area in the clinical setting of pancreatitis [8–11], whereas only a few studies have discussed intratumoral cystic lesions, such as cystic necroses, in larger ordinary PDACs [6, 7]. Some case reports have described the intratumoral cystic changes of PDAC variants, i.e. adenosquamous carcinoma [12], mucinous adenocarcinoma (colloid or mucinous non-cystic carcinoma) [13], osteoclast-like giant cell carcinoma [14] and pleomorphic giant cell carcinoma [15]. To the best of our knowledge, there have been no radiological reports regarding the intratumoral cystic lesions of ordinary PDAC. Compared with CT, MRI has the advantage of being able to detect cystic changes within pancreatic masses and to provide more accurate morphological detail on these changes [16]. Therefore, the aims of this study were to evaluate intratumoral cystic lesions of ordinary PDAC detected on MRI and to correlate the cystic lesions with their histopathological findings.     

Compromised perfusion in femoral head in normal rats: distinctive perfusion MRI evidence of contrast washout delay

Objectives

The femoral head is prone to osteonecrosis. This study investigated dynamic contrast-enhanced (DCE) MRI contrast washout features of the femoral head and compared the data with data from other bony compartments in normal rats.

Methods

7-month-old Wistar rats were used. DCE MRI of the right hip (n=18), right knee (n=12) and lumbar spine (n=10) was performed after an intravenous bolus injection of Gd-DOTA (0.3 mmol kg^–1). Temporal resolution was 0.6 s for hip and spine, and 0.3 s for knee. The total scan duration was 8 min for hip and spine, and 4.5 min for knee. The regions of interest for enhancement measurement included femoral head, proximal femoral diaphysis, distal femoral diaphysis and epiphysis, proximal tibial epiphysis and diaphysis, and lumbar vertebrae L1–5.

Results

Femoral head showed no enhancement signal decay during the DCE MRI period, while all other bony compartments showed a contrast washin phase followed by a contrast washout phase. In the knee joint, the contrast washout of the proximal tibia diaphysis was slower that of other bony compartments of the knee.

Conclusion

Based on the evidence of delayed contrast washout, this study showed that blood perfusion in the femoral head could be compromised in normal rats.Clinical studies have shown that the femoral head has a poorer blood supply compared with the femoral neck and femoral shaft [1,2]. MRI-derived perfusion indices of maximum enhancement and enhancement slope for the femoral head were only about one-fifth to one-quarter of those for the femoral shaft in healthy elderly male and female subjects [1]. Because of the absence of an effective collateral circulation, the femoral head is at an especially high risk of ischaemic injury [3]. Osteonecrosis of the femoral head may be idiopathic or secondary to numerous diseases. Bone perfusion can affect bone metabolism and microdamage repair. Osteonecrosis can have early vascular components that change underlying bone perfusion in the affected bone and joint, and contribute to the clinical cascade of disease [4]. Relatively mild haemodynamic impairment, which may not necessarily compromise other sites, has the potential to cause osteonecrosis of the femoral head [1,5,6]. In animals, osteonecrosis of the femoral head is sporadically encountered in dogs [7]. Perthes disease-like necrosis of the femoral head and neck occurs in some breeds of small dogs [7]. Osteonecrosis of the femoral head is also seen in spontaneously hypertensive rats [8-10]. Recently it was reported that delayed washout in dynamic contrast-enhanced (DCE) MRI suggests compromised blood perfusion in the tissue, including blood stasis or outflow obstruction [11]. It was also reported that delayed contrast washout could be seen in sites of bone marrow oedema, osteoarthritis and avascular osteonecrosis [11]. This study investigated DCE MRI contrast washout features of the femoral head in normal mature rats. The results from the femoral head were compared with the data from proximal and distal femoral diaphysis, distal femoral epiphysis, proximal tibial epiphysis and diaphysis, and lumbar vertebral bodies.     

The effect of gadoxetic acid enhancement on lesion detection and characterisation using T₂ weighted imaging and diffusion weighted imaging of the liver

Objectives

To evaluate the effect of gadoxetic acid enhancement on the detection and characterisation of focal hepatic lesions on T₂ weighted and diffusion weighted (DW) images.

Methods

A total of 63 consecutive patients underwent T₂ weighted and DW imaging before and after gadoxetic acid enhancement. Two blinded readers independently identified all of the focal lesions using a five-point confidence scale and characterised each lesion using a three-point scale: 1, non-solid; 2, indeterminate; and 3, solid. For both T₂ weighted and DW imaging, the accuracies for detecting focal lesions were compared using the free-response receiver operating characteristic analysis; the accuracies for lesion characterisation were compared using the McNemar test between non-enhanced and gadoxetic acid-enhanced image sets. For hepatic lesions ≥1 cm, the lesion-to-liver contrast-to-noise ratio (CNR) and the apparent diffusion coefficient (ADC) were compared in the non-enhanced and enhanced image sets using the generalised estimating equations.

Results

For both T₂ weighted and DW images, the accuracies for detecting focal lesions (p≥0.52) and those for lesion characterisation (p≥0.63) did not differ significantly between the non-enhanced and enhanced image sets. The lesion-to-liver CNR was significantly higher on enhanced DW images than on non-enhanced DW images (p=0.02), although the difference was not significant for T₂ weighted imaging (p=0.65). The mean ADC values of lesions did not differ significantly on enhanced and non-enhanced DW imaging (p=0.75).

Conclusion

The acquisition of T₂ weighted and DW images after administration of gadoxetic acid has no significant effect on the detection or characterisation of focal hepatic lesions, although it improves the lesion-to-liver CNR on DW images.Various contrast agents have been developed and utilised for MRI of the liver in order to facilitate the detection and characterisation of focal hepatic lesions. Gadoxetic acid (gadolinium-ethoxybenzyl-diethylenetriamine pentaacetic acid, Primovist^®; Bayer Schering Pharma, Berlin, Germany) is a recently developed, liver-specific contrast agent. As it has combined extracellular and hepatocyte-specific properties, gadoxetic acid can provide functional information regarding the cellular composition of focal hepatic lesions on hepatobiliary phase imaging as well as haemodynamic information on dynamic MRI following bolus injection. These properties of gadoxetic acid have been reported to improve the accuracy of liver MRI for lesion detection and characterisation [1-7].By contrast, these advantages of gadoxetic acid-enhanced liver MRI are obtained with increased examination time, as delayed scanning approximately 20 min after contrast administration is necessary for optimal hepatobiliary phase imaging [4,5,7-9]. Among the pulse sequences commonly acquired for clinical liver MRI, T₂ weighted and diffusion weighted (DW) imaging are frequently performed using a respiratory-triggered method in order to improve image quality [10-12], thus a lengthy acquisition time is required. To shorten the examination time for gadoxetic acid-enhanced MRI, it has been proposed to perform respiratory-triggered T₂ weighted and DW imaging during the interval between dynamic T₁ weighted imaging and the hepatobiliary phase imaging [7,13,14]. However, this modification in the MRI protocol is only feasible if the administration of gadoxetic acid does not degrade the image quality and provides comparable image quality and accuracy to non-enhanced imaging.Although previous studies have demonstrated that gadolinium-enhanced T₂ weighted images improve the conspicuity of focal hepatic lesions compared with unenhanced T₂ weighted images [15,16], these studies used non-specific extracellular contrast agents. Considering the different properties of extracellular contrast agents and gadoxetic acid, these results might not be easily applied to gadoxetic acid-enhanced MRI.Therefore, the purpose of our study was to evaluate the effect of gadoxetic acid on lesion detection and characterisation using T₂ weighted and DW imaging.     

Diffusion-weighted MRI findings of treated and untreated retroperitoneal fibrosis

PURPOSE

We aimed to evaluate diffusion-weighted imaging (DWI) findings in patients with treated and untreated retroperitoneal fibrosis (RPF).

METHODS

We analyzed magnetic resonance imaging examinations of 44 RPF patients (36 male, 8 female), of which 15 were untreated and 29 were under therapy. Qualitative DWI and T1 postcontrast signal intensities and the largest perivascular extent of RPF were compared between treated and untreated groups and correlated to erythrocyte sedimentation rate and C-reactive protein values. Quantitative DWI signal intensities and apparent-diffusion-coefficients were calculated in regions-of-interest, together with a relative index between signal intensities of RPF and psoas muscle in 15 untreated patients and 14 patients under treatment with remaining perivascular fibrosis of more than 5 mm.

RESULTS

The extent of RPF in untreated patients was significantly larger compared with the extent of RPF in treated patients (P < 0.0001). DWI signal intensities were significantly higher in untreated patients than in patients under therapy (mean, 27 s/mm² vs. 20 s/mm²; P = 0.009). The calculated DWI-index was significantly higher in untreated patients than in patients under therapy (P = 0.003).

CONCLUSION

Our data show significant differences in the DWI findings (b800 signal intensities and relative DWI-index) of patients with treated and untreated RPF. DWI is a promising technique in the assessment of disease activity and the selection of patients suitable for medical therapy.Retroperitoneal fibrosis (RPF) is a rare disease affecting the retroperitoneal space (1–3). It presents as retroperitoneal proliferation of fibrous tissue surrounding the retroperitoneal vascular structures and abutting the medial aspect of the ureters. Clinical findings of RPF are non-specific; the most common symptom is chronic back pain. Further symptoms include lower extremity edema, deep vein thrombosis, oliguria, and urinary tract infection (3). Computed tomography (CT) and magnetic resonance imaging (MRI) are the preferred imaging modalities for the diagnosis of RPF (3). Retroperitoneal fibrosis shows contrast enhancement of gadolinium containing contrast media in MRI (4). Medical treatment is classically based on steroids like prednisone (3). Recent studies suggested tamoxifen as another safe and effective treatment alternative (5).The assessment of disease activity is relevant for planning of further medical or surgical therapy (6, 7). Nowadays the disease activity is assessable by positron emission tomography tracer uptake (3), with a relatively low resolution and the need of ionized radiation. As an alternative, dynamic contrast-enhanced MRI was suggested for the evaluation of disease activity (7, 8). However, gadolinium may be contraindicated in patients with impaired renal function due to the potential development of nephrogenic systemic fibrosis (NSF) (9). This is especially relevant in RPF patients with postrenal failure due to ureteral compression. For those cases a supplemental method for the determination of disease activity would be helpful.Diffusion-weighted imaging (DWI) is a radiation-free unenhanced MRI modality that has been applied for the detection of bowel inflammation in patients with chronic inflammatory bowel diseases (10, 11), as well as for oncological retroperitoneal and abdominal applications (12–14). Therefore, we aimed to evaluate the application and findings of DWI in patients with treated and untreated RPF disease.     

MRI evaluation of neoadjuvant low-dose fractionated radiotherapy with concurrent chemotherapy in patients with locally advanced breast cancer

Objectives

We address the diagnostic performance of breast MRI and the efficacy of neoadjuvant radiochemotherapy (NRC) treatment (NRC protocol) vs conventional neoadjuvant chemotherapy (NAC) in patients with locally advanced breast cancer.

Methods

The NRC protocol consists of six anthracycline/taxane cycles and concomitant low-dose radiotherapy on breast tumour volume. Breast MRI was performed at baseline and after the last therapy cycle in 18 and 36 patients undergoing the NRC protocol or conventional NAC (propensity matching).

Results

In both groups, we observed reduced tumour dimensions after the last cycle (p<0.001), and the response evaluation criteria in solid tumours (RECIST) class directly correlated with the tumour regression grade class after the last cycle (p<0.001). Patients in the NRC group displayed a higher frequency of complete/partial response than those in the NAC group (p=0.034). 17 out of 18 patients in the NRC group met the criteria for avoiding mastectomy based on final MRI evaluation. The RECIST classification displayed a superior diagnostic performance in the prediction of the response to treatment [area under the receiver operating characteristic curve (AUC)=0.72] than time-to-intensity curves and apparent diffusion coefficient (AUC 0.63 and 0.61). The association of the three above criteria yielded a better diagnostic performance, both in the general population (AUC=0.79) and in the NRC and the NAC group separately (AUC=0.82 and AUC=0.76).

Conclusions

The pathological response is predicted by MRI performed after the last cycle, if both conventional MRI and diffusion imaging are integrated. The NRC treatment yields oncological results superior to NAC.

Advances in knowledge

MRI could be used to establish the neoadjuvant protocol in breast cancer patients.Neoadjuvant chemotherapy is currently widely employed in patients with locally advanced breast cancer (LABC) in order to improve the rate of breast-conserving surgery (up to 98% of patients) and systemic control of the disease [1,2]. The coupling of pre-operative radiotherapy (RT) cycles with neoadjuvant chemotherapy has been proposed for other cancer types. In particular, taxanes could have a synergistic effect with RT when administered concurrently [3-5]. Nonetheless, few data are currently available on the efficacy of concurrent neoadjuvant RT in patients with LABC, although evidence exists that such a strategy is safe and feasible [6], and is supported by preliminary investigations [7,8]. Radiation doses below 0.5 Gy have been demonstrated to enhance the effectiveness of continuous-infusion taxanes. This phenomenon has been termed low-dose hyper-radiosensitivity [9,10].MRI is a reliable tool to evaluate the breast cancer response to chemotherapy by measuring tumour diameter changes and by assessing the viability of residual tumour areas [11-13]. Nevertheless, MRI may under- or overestimate the burden of residual tumour by confounding a fibrotic scar with viable tumour tissue, or vice versa. Diffusion-weighted imaging (DWI) has been shown in such contexts to improve the diagnostic performance of MRI [14]. It has not been clarified whether MRI retains its diagnostic performance even in the context of breast RT. The latter is known to trigger tissue oedema, which may potentially impair the diagnostic accuracy [15,16]. The purpose of the present work is to ascertain (1) the diagnostic performance of MRI and DWI-MRI in the context of concurrent low-dose fractionated RT (LD-FRT) and chemotherapy in the prediction of response to neoadjuvant treatment; (2) whether the adoption of concurrent neoadjuvant LD-FRT and chemotherapy yields better oncological results in LABC than neoadjuvant chemotherapy alone.     

Quantitative pixelwise myocardial perfusion maps from first-pass perfusion MRI

Objective:

To calculate and evaluate absolute quantitative myocardial perfusion maps from rest first-pass perfusion MRI.

Methods:

10 patients after revascularization of myocardial infarction underwent cardiac rest first-pass perfusion MRI. Additionally, perfusion examinations were performed in 12 healthy volunteers. Quantitative myocardial perfusion maps were calculated by using a deconvolution technique, and results were compared were the findings of a sector-based quantification.

Results:

Maps were typically calculated within 3 min per slice. For the volunteers, myocardial blood flow values of the maps were 0.51 ± 0.16 ml g⁻¹ per minute, whereas sector-based evaluation delivered 0.52 ± 0.15 ml g⁻¹ per minute. A t-test revealed no statistical difference between the two sets of values. For the patients, all perfusion defects visually detected in the dynamic perfusion series could be correctly reproduced in the maps.

Conclusion:

Calculation of quantitative perfusion maps from myocardial perfusion MRI examinations is feasible. The absolute quantitative maps provide additional information on the transmurality of perfusion defects compared with the visual evaluation of the perfusion series and offer a convenient way to present perfusion MRI findings.

Advances in knowledge:

Voxelwise analysis of myocardial perfusion helps clinicians to assess the degree of tissue damage, and the resulting maps are a good tool to present findings to patients.MRI is widely used for the evaluation of myocardial perfusion. Advantages of perfusion MRI are a higher spatial resolution compared with positron emission tomography (PET)^1,2 and single photon emission CT³ and the lack of exposure to radiation. Great efforts have been made to use MRI for quantitative evaluation of myocardial perfusion in the past years.^4,5 In clinical routine, however, evaluation of MRI perfusion examinations is performed by the visual analysis of the acquired images depicting areas remaining hypo-intense during the passage of the contrast agent bolus. One main reason for not quantifying myocardial perfusion is the sometimes-excessive user interaction time required for manual segmentation of the acquired images in the quantification process.If myocardial perfusion is quantified, in most studies, the high spatial resolution of the acquired MR images is not maintained. Instead, a sector-based evaluation is performed.^6,7 First attempts have been made to calculate myocardial perfusion maps to evaluate regional myocardial perfusion.^3,8–10 However, until now, these studies were performed in animals^8–10 or perfusion was only evaluated semiquantitatively.³ Recently, our group has published an automatic post-processing tool for quantitative perfusion evaluation.¹¹ That study focused on the automation of post-processing but confined itself on sectors of the myocardium. The next and consequent step is to evolve this technique to work on a pixel-by-pixel basis. Therefore, it was the goal of this study to develop and test a method that calculates pixelwise quantitative perfusion maps from myocardial perfusion MRI examinations. These maps might help the clinician in making a diagnosis by decreasing the number of images to be examined, because a pixelwise quantitative perfusion map demonstrates the information of a whole series of images obtained in a first-pass perfusion examination clearly arranged.     

Correlation of the apparent diffusion coefficiency values on diffusion-weighted imaging with prognostic factors for breast cancer

Objective

The aim of this study was to correlate the apparent diffusion coefficient (ADC) value of breast cancer with prognostic factors.

Methods

335 patients with invasive ductal carcinoma not otherwise specified (IDC NOS) and ductal carcinoma in situ (DCIS) who underwent breast MRI with diffusion-weighted imaging were included in this study. ADC of breast cancer was calculated using two b factors (0 and 1000 s mm^–2). Mean ADCs of IDC NOS and DCIS were compared and evaluated. Among cases of IDC NOS, mean ADCs were compared with lymph node status, size and immunochemical prognostic factors using Student''s t-test. ADC was also correlated with histological grade using the Kruskal–Wallis test.

Results

Mean ADC of IDC NOS was significantly lower than that of DCIS (p<0.001). However, the mean ADC of histological grade of IDC NOS was not significantly different (p=0.564). Mean ADC of oestrogen receptor (ER)-positive or progesterone receptor (PR)-positive cancer was significantly lower than that of ER-negative or PR-negative cancer (p=0.003 vs p=0.032). Mean ADC of Ki-67 index-positive cancer was significantly lower than that of Ki-67 index-negative cancer (p=0.028). Mean ADC values of cancers with increased microvascular density (MVD) were significantly lower than those of cancer with no MVD increase (p=0.009). No correlations were observed between mean ADC value and human growth factor receptor 2 expression, tumour size and lymph node metastasis.

Conclusion

Low ADC value was correlated with positive expression of ER, PR, increased Ki-67 index, and increased MVD of breast cancer.Breast MRI is an established supplemental technique to mammography and ultrasonography for evaluation of suspicious breast lesions. Diffusion-weighted MRI (DWI) has recently been integrated into the standard breast MRI for discrimination of benign and malignant breast lesions obtained with dynamic contrast-enhanced MRI [1-13]. DWI is a non-invasive technique that represents the biological character of the mainly Brownian movement of protons in bulk water molecules in vivo. Apparent diffusion coefficient (ADC) values are quantified by measurement of mean diffusivity along three orthogonal directions, which are affected by cellularity of the tissue, fluid viscosity, membrane permeability and blood flow [7,9-11]. Microstructural characteristics, including water diffusion and blood microcirculations in capillary networks, were associated with ADC value. Decreased movement of molecules in highly cellular tissue showed correlation with a low ADC value [3,4]. Several studies of DWI of the breast have reported significantly lower ADC values in malignant tumours, compared with benign breast lesions and normal tissue [1-3,5-11,14]. Classic prognostic markers, including tumour size and grade, and lymph node status in patients with breast cancer, and molecular markers, including oestrogen receptor (ER), progesterone receptor (PR), Ki-67 index, human growth factor receptor 2 (HER2) protein and angiogenic molecular markers, have been reported [1,15,16]. Few studies have examined the correlation between ADC values and prognostic factors [1,8]. The purpose of this study is to compare ADC values of DWI of breast cancer with prognostic factors.     

Contrast-enhanced MRI of the subdeltoid,subacromial bursa in painful and painless rotator cuff tears

Objective

Although shoulder pain is often associated with rotator cuff tears, many tears are asymptomatic and are not the cause of the patient''s pain. This may explain the persistence of symptoms in some patients despite technically successful rotator cuff repair. It has been proposed that rotator cuff tears cause pain through subdeltoid/subacromial bursal inflammation. The aim of this study was to determine whether bursal inflammation seen on MRI is associated with pain in patients with rotator cuff tears of the shoulder.

Methods

The shoulders of 255 patients were screened with ultrasound. 33 full-thickness rotator cuff tears (18 with shoulder pain and 15 without pain) were identified and subsequently studied using contrast-enhanced MRI of the shoulder. Enhancement of the subacromial bursa was scored independently by two musculoskeletal radiologists. Logistic regression was used to determine whether bursal enhancement was independently associated with pain.

Results

There was a significant association between pain and age, with greater likelihood of pain in younger patients. Bursal enhancement was common in both painful and painless tears. No statistically significant link between pain and bursal enhancement was seen, even after accounting for age.

Conclusion

Although enhancement of the subdeltoid/subacromial bursa was common, no evidence was found to support the hypothesis that bursal enhancement is associated with pain in rotator cuff tears. It is therefore unlikely to determine reliably which patients would benefit from rotator cuff repair.

Advances in knowledge

Bursal enhancement and thickening does not reliably correlate with symptoms or presence of rotator cuff tear.Rotator cuff tears are a common cause of pain in the shoulder. Surgical repair is an effective treatment, but a significant proportion of patients (5–12.5%) fail to achieve a satisfactory outcome [1-4]. Long-term outcome of surgery correlates poorly with the integrity of the cuff repair [5-7] and persistence of pain is a major factor [1]. In some cases, this may be because the shoulder pain is not due to rotator cuff damage at all [8]. Other painful shoulder pathologies are common, particularly in the elderly, including glenohumeral and acromioclavicular arthritis [9], and bone marrow oedema [10]. Asymptomatic rotator cuff tears are common, with increasing incidence with age and a reported prevalence of up to 80% in subjects aged over 80 years [11]. A significant proportion of these are full-thickness tears with one study reporting full-thickness tears in 28% of people over the age of 60 [12]. Rotator cuff tears may remain asymptomatic despite their large size [13] and, although the size of tears often increases, symptoms may develop or resolve with conservative treatment [14-16]. As yet there is no clear consensus regarding the indications for rotator cuff surgery [17,18]. A technique to determine whether a known rotator cuff tear is responsible for an individual patient''s pain would therefore be of great clinical value in developing patient management plans. While MRI has been shown to be accurate for detecting rotator cuff tears [19,20], there is no convincing evidence to date that it can be used to determine whether a full-thickness tear is symptomatic [12,21].The mechanism by which rotator cuff tears cause pain is poorly understood. Tears are associated with histological inflammation of the subdeltoid/subacromial bursa and this has recently been proposed as a cause of pain [22]. Synovial inflammation in the bursa in symptomatic rotator cuff tears could potentially be detected by the associated enhancement in the inflamed bursa seen on MRI after the administration of intravenous contrast agent, in the same way that synovial volume in joints in inflammatory arthritis has been shown to correlate with histological measures of inflammation [23]. The aim of this study was to use contrast-enhanced MRI to assess subacromial bursitis in patients with painful and painless rotator cuff tears in order to test the hypothesis that synovial enhancement at the subacromial bursa is greater in patients with shoulder pain.     

Screening for atherosclerotic plaques in the abdominal aorta in high-risk patients with multicontrast-weighted MRI: a prospective study at 3.0 and 1.5 tesla

Objective

This prospective study compares MRI of atherosclerotic plaque in the abdominal aorta at 3 T with that at 1.5 T in patients suffering from hereditary hyperlipidaemia, a major risk factor for atherosclerosis.

Methods

MRI of the abdominal aorta at 1.5 and 3 T was performed in 21 patients (mean age 58 years). The study protocol consisted of proton density (PD), T₁, T₂ and fat-saturated T₂ weighted black blood images of the abdominal aorta in corresponding orientation. Two independent radiologists performed image rating. First, image quality was rated on a five-point scale. Second, atherosclerotic plaques were scored according to the modified American Heart Association (AHA) classification and analysed for field strength-related differences. Weighted κ statistics were calculated to assess interobserver agreement.

Results

Interobserver agreement was substantial for nearly all categories. MRI at 3 T offered superior image quality in all contrast weightings, most significantly in T₁ and T₂ weighted techniques. Plaque burden in the study collective was unexpectedly moderate. The majority of plaques were classified as AHA III lesions; no lesions were classified above AHA V. There was no significant influence of the field strength regarding the AHA classification.

Conclusion

Abdominal aortal plaque screening is basically feasible at both field strengths, whereas the image quality is rated superior at 3 T. However, the role of the method in clinical practice remains uncertain, since substantial findings in the high-risk collective were scarce.Atherosclerosis is a systemic disease of the vessel wall that mainly occurs in medium-sized and large arteries; its thrombotic or thromboembolic complications are the main cause of mortality and morbidity in industrialised countries [1,2]. It is characterised by a thickening of the vessel wall, especially the intima, and is histologically composed of a lipid core with an overlying fibrous cap. The main plaque components are fibrous elements (e.g. connective tissue, collagen, proteoglycans), lipids (e.g. cholesterol, phospholipids), smooth muscle cells and inflammatory cells (e.g. macrophages, T lymphocytes). The composition of the atherosclerotic plaque determines its vulnerability [3-6]. The so-called “vulnerable plaque” consists of a large lipid core and a thin fibrous cap, although the characteristics of the vulnerable plaques vary depending on the arterial region (i.e. coronaries, carotids, aorta) [6-8]. Rupture of atherosclerotic plaques as a result of an endothelial lesion is the most frequent cause of the unpredictable onset of acute thromboembolic vascular events such as myocardial infarction, ischaemic stroke or sudden cardiac death [9,10]. Therefore, it is necessary to characterise plaque components and determine them at an early stage to prevent cardiovascular events. Several invasive and non-invasive imaging modalities are used to study atherosclerotic vessel lesions: conventional (B-mode) ultrasound, intravascular ultrasound (IVUS), conventional angiography, CT, angioscopy and MRI [5,10]. Most of them identify luminal diameter or stenosis, wall thickness and plaque volume, but are not able to determine plaque components [5,11]. Several recent studies showed that in vivo and ex vivo MRI as a non-invasive method can characterise the composition of atherosclerotic plaques such as fibrous tissue, lipid core, calcification, haemorrhage and thrombus [5,10,12-18]. The aim of this characterisation is the determination of the risk of plaque rupture.Most of the previous publications regarding plaque imaging in the human aorta are of studies performed at 1.5 T. Newer publications show the advantages of high field strength, such as faster imaging with parallel imaging techniques and higher signal-to-noise ratio (SNR) [19,20].The purpose of this study was to compare in vivo multimodality MR plaque imaging of the human aorta at 1.5 T and 3 T in a patient collective at high risk for atherosclerosis, in which atherosclerotic wall alterations can be expected. The evaluation focused on image quality and on the analysis of atherosclerotic plaque components according to the American Heart Association (AHA) classification [3,21].In the context of the prospective study, plaque imaging was always performed in addition to whole-body MR angiography (WBMRA) and is therefore part of a whole-body screening approach.     

Prognostic significance of parameters derived from co-registered 18F-fluorodeoxyglucose PET and contrast-enhanced MRI in patients with high-grade glioma

Objective

The aim of this study was to determine the prognostic significance of the volume and intensity of abnormal ¹⁸F-fluorodeoxyglucose positron emission tomography (FDG-PET) accumulation within areas of contrast enhancement on post-therapeutic volumetric MRI.

Methods

A total of 10 patients with Grade III or IV glioma were treated with resection followed by intracavitary radiation therapy with ¹³¹I-labelled antitenascin monoclonal antibody. Patients underwent serial FDG-PET and 1.5 T MR imaging. For each patient, MR and FDG-PET image volumes at each time point were aligned using a rigid-body normalised mutual information algorithm. Contrast-enhancing regions of interest (ROIs) were defined using a semi-automated k-means clustering technique. Activity within the ROI on the co-registered PET scan was calculated as a ratio (mean activity ratio; MAR) to activity in contralateral normal-appearing white matter (NAWM). The PET lesion was defined as the portion of the ROI associated with activity greater than two standard deviations above the mean in NAWM. Survival was assessed using the logrank test.

Results

Larger contrast-enhancing ROIs were strongly associated with an increased MAR (r = 0.51; p<0.002). Enhancing lesions with an MAR >1.2 were associated with decreased survival (p<0.016). In nine patients who died, the MAR on PET correlated inversely with survival duration (r = −0.43; p<0.01), whereas PET lesion volume did not.

Conclusion

Following intracavitary radiation therapy, the development of contrast-enhancing lesions that are associated with high mean FDG-PET accumulation suggests poor prognosis.High-grade gliomas are the most common primary central nervous system (CNS) tumours, having a combined incidence of 5–8/100 000 population [1]. Even with optimal management of these tumours, consisting of complete surgical resection, radiation therapy and adjuvant temozolomide, median overall survival in these patients approximates 1 year [2]. Despite recent advances, genotypic heterogeneity within pathologically indistinguishable tumours remains a major barrier to successful treatment of patients with high-grade primary brain tumours [3]. As a result of this heterogeneity, only a minority of individual tumours are likely to respond to any given chemotherapeutic agent [4]. Early identification of non-responders would allow more effective therapy to be instituted, while minimising the morbidity and financial cost associated with prolonged ineffective treatment. At present, contrast-enhanced MRI provides the primary imaging assessment of therapeutic efficacy in such patients, but the shortcomings of this paradigm are well known [4-6]. Positron emission tomography (PET) using the radiotracer ¹⁸F-fluorodeoxyglucose (FDG) has a complementary role to MRI in the evaluation of primary cerebral malignancies, providing in vivo physiological information not otherwise available [7]. The glucose metabolic rate of such tumours has been shown to be an accurate predictor of histological tumour grade as well as of patient survival, information that often effects management [8-10]. Although it was first demonstrated in the de novo evaluation of such tumours, there is some evidence that this relationship might also apply in the setting of prior therapeutic intervention [11^,12]. Furthermore, at least two groups have been able to establish thresholds of FDG accumulation above which patients are likely to have poor prognosis [9^,13]. These data demonstrate the potential for quantitative analysis of FDG-PET imaging to prospectively evaluate therapeutic efficacy in individual patients with high-grade brain tumours.The potential utility of FDG-PET imaging towards this end, however, will require the development of parameters with a degree of test–retest reproducibility. To accomplish this goal, two major challenges must be overcome: the high glucose metabolism within normal grey matter and regional tumour heterogeneity. Cerebral grey matter uses glucose almost exclusively to meet its energy requirements. As a result, normal cortex and deep grey matter nuclei have high baseline FDG accumulation, making differentiation from high-grade neoplasm a significant challenge. A common solution to this problem is side-by-side anatomical correlation with contrast-enhanced MR images [6^,9^,13]. Although image analysis can be accomplished in this manner, different angles of image acquisition can make accurate correlation difficult [6]. By accounting for these differences, formal co-registration of anatomical and FDG-PET data might provide more accurate characterisation of intracranial lesions [6^,14]. Considering the second challenge, malignant primary brain tumours display a high degree of regional histological heterogeneity; the majority of tumours display elements of both high and low World Health Organization (WHO) grade [6^,15]. Current strategies for region of interest (ROI) selection typically involve subjective placement of ROIs using side-by-side comparison with MR images [9^,13]. Such strategies are unlikely to include the same regions of the tumour on sequential examinations and will therefore likely serve to diminish the reproducibility of quantitative measures of FDG accumulation. Methods that analyse FDG accumulation within whole-tumour ROIs might be less susceptible to variability resulting from intratumoural heterogeneity. It is important to note, however, that such analyses might not have the same prognostic value, given evidence that tumour behaviour might be best predicted by its most FDG-avid elements [16].The goal of this study was to evaluate the prognostic significance of parameters of FDG accumulation within whole-tumour ROIs derived from co-registered FDG-PET and contrast-enhanced MRI exams. As the patterns of FDG accumulation within areas of tumour-related enhancement have not been well characterised, we also sought to examine the relationship between quantitative parameters derived from the two imaging studies.