Giant Cell Tumor with Secondary Aneurysmal Bone Cyst Shows Heterogeneous Metabolic Pattern on <Superscript>18</Superscript>F-FDG PET/CT: A Case Report

Giant cell tumor (GCT) is a generally benign bone tumor accounting for approximately 5 % of all primary bone neoplasms. Cystic components in GCTs that indicate secondary aneurysmal bone cysts (ABCs) are reported in 14 % of GCTs. Although both of them have been described separately in previous reports that may show considerable fluorodeoxyglucose (FDG) uptake despite their benign nature, the findings of GCT with secondary ABC on ¹⁸F-FDG positron emission tomography/computed tomography (PET/CT) have not been well-known. We report a case of GCT with secondary ABC in a 26-year-old woman. ¹⁸F-FDG PET/CT revealed a heterogeneous hypermetabolic lesion in the left proximal femur with the maximum standardized uptake value of 4.7. The solid components of the tumor showed higher FDG uptake than the cystic components. These observations suggest that the ABC components in GCTs show heterogeneous metabolic patterns on ¹⁸F-FDG PET/CT.     

Multicentric Primary Angiosarcoma of Bone Mimicking Metastasis on 18F-FDG PET/CT in a Patient with a History of Sigmoid Colon Cancer: a Case Report

Primary angiosarcoma of the bone (PAB) is a rare and fatal high-grade malignant vascular bone tumor. We report a rare case of multicentric PAB mimicking bone metastasis in a 59-year-old female patient with a history of sigmoid colon cancer. This patient complained of lower back and pelvic pain and presented with multiple osteolytic bone lesions on plain radiography and pelvic computed tomography. First, bone metastasis of sigmoid colon cancer was suspected. However, on the ¹⁸F-fluorodeoxyglucose (¹⁸F-FDG) positron emission tomography/computed tomography (PET/CT) scan, the patient presented unusual multiple hypermetabolic osteolytic bone lesions involving contiguous bones of the lower half of the body. After bone biopsy, these lesions were confirmed to be multicentric PAB. To the best of our knowledge, this is the first case report of an ¹⁸F-FDG PET/CT scan in a patient with multicentric primary bone angiosarcoma.     

<Superscript>18</Superscript>F-FDG PET/CT Imaging of Pulmonary Mucinous Cystadenocarcinoma with Signet Ring Cells

A 63-year-old male with a recently diagnosed right lung lesion was referred for staging. F-FDG PET/CT scan revealed a hypodense, cystic-like mass in the right upper lung lobe, which demonstrated low, diffuse ¹⁸F-FDG uptake, likely due to the presence of mucus, as well as intensely hypermetabolic right hilar and right paratracheal lymph nodes. Transbronchial biopsy revealed a primary pulmonary mucinous cystadenocarcinoma with the presence of signet ring cell carcinoma, a co-existence of two rare variants of lung adenocarcinoma. This case report demonstrates the metabolic phenotype along with the radiographic characteristics of this rare tumor and its metastases.     

Iatrogenic lung microembolism detected by 18FDG PET/CT

We present the cases of two oncology patients: a male with Hodgkin's disease after completion of chemotherapy, and a woman recently diagnosed of melanoma, who underwent positron emission tomography/computed tomography (PET/CT) with 18F-FDG for therapeutic monitoring and initial staging, respectively. In both cases, hypermetabolic foci of 18F-FDG in lung parenchyma were found, without morphologic abnormalities in CT. These findings would have been consistent with lung pathology in the absence of any anatomic correlation. Combined PET/CT interpretation was of lung microembolisms probably originated at the injection site.     

Unsuspected Active Sarcoidosis Diagnosed by 18F-FDG PET/CT During the Search for a Primary Tumour in a Patient with Bone Lesions

Sarcoidosis is a systemic chronic inflammatory disease of unknown aetiology, characterised by granulomatous lesions with heterogeneous clinical manifestations affecting multiple organs and tissues. Although the respiratory system is most commonly affected, the disease may also present with bone lesions. We report the case of a 31-year-old woman who presented with low back pain and no history of cancer and who was found to have suspicious lesions involving the entire spine on magnetic resonance imaging (MRI). The patient underwent 18F-fluorodeoxyglucose (FDG) PET/CT to search for a primary tumour and for staging purposes. 18F-FDG PET/CT revealed a pattern of hypermetabolic activity in widespread skeletal lesions and in a single left cervical lymph node. The primary tumour was not found, thus suggesting a haematologic disorder. Subsequent biopsies of a cervical lymph node and of bone tissue from L4 revealed active sarcoidosis with no evidence of cancer. This underlines the importance of considering all alternatives when hypermetabolic lesions are found on 18F-FDG PET/CT. Furthermore, 18F-FDG PET can be very useful to indicate accessible sites for guiding fine-needle aspiration cytology (FNAC).     

Peripheral bone involvement of intravascular large B-cell lymphoma on 99mTc-MDP bone scan and 18F-FDG PET/CT

A 64-year-old man was admitted for evaluation of recently developed anemia and bone pain. The bone scan showed diffusely active lesions in the peripheral bones, symmetrically. Interestingly, 18F-FDG PET/CT revealed the hypermetabolic changes in the peripheral bones as well as the internal organs. Biopsy of bone marrow confirmed the diagnosis of intravascular B-cell lymphoma. After the 3 cycles of R-CHOP chemotherapy, 18F-FDG PET/CT showed improvement of the previous hypermetabolic lesions, suggesting good response. Intravascular B-cell lymphoma is a rare and aggressive variant of diffuse large cell lymphoma characterized by proliferation of malignant cells within the vascular lumina.     

18F-FDG PET/CT在胃癌中的临床应用进展

胃癌是全球范围内最常见的恶性肿瘤之一。18F-氟脱氧葡萄糖（FDG）PET/CT在胃癌中的应用既有优点又有局限性。胃癌原发灶对18F-FDG的摄取与癌症分期、组织学分型和肿瘤大小密切相关。早期胃癌18F-FDG摄取阳性预示着内镜黏膜下剥离术的不可治愈性。进展期胃癌的最大标准化摄取值（SUV_max）在肠型与印戒细胞癌（SRC）或弥漫型胃癌间的差异显著,SRC的SUV_max与患者的总生存时间和无病生存时间呈负相关。18F-FDG PET/CT对区域淋巴结转移的诊断灵敏度较低,但其特异度很高,区域淋巴结对18F-FDG摄取呈阳性是预后不良的指征。18F-FDG PET/CT可检出隐匿的远处转移（7.2%~10.0%）,其中大部分（4.7%~8.8%）使用腹腔镜也不能检出。常规性应用18F-FDG PET/CT并联合腹腔镜检查对明确胃癌分期的意义重大。因此,笔者就18F-FDG PET/CT在胃癌中的临床应用进展进行综述。     

Localization of dystonic muscles with 18F-FDG PET/CT in idiopathic cervical dystonia.

The purpose of this study was to investigate whether (18)F-FDG PET/CT is useful for localizing dystonic cervical muscles in patients with idiopathic cervical dystonia (ICD) by comparing disease severity before and disease severity after botulinum toxin (BT) injection into hypermetabolic muscles. METHODS: Six patients with ICD underwent (18)F-FDG PET/CT. Dystonic muscles suitable for BT injection therapy were defined as those showing diffusely increased (18)F-FDG uptake. RESULTS: Hypermetabolic cervical muscles were identified in all 6 patients. In 2 patients who underwent PET/CT both in a supine position and in a sitting position during (18)F-FDG uptake, abnormal hypermetabolic muscles were observed by PET/CT only when patients were in the sitting position with their heads and necks in the adopted abnormal involuntary posture. Symptoms were significantly improved in 4 patients who underwent BT injection therapy guided by PET/CT and who were clinically monitored. CONCLUSION: (18)F-FDG PET/CT is potentially useful for identifying dystonic cervical muscles for BT therapy in patients with ICD.     

PET/CT in malignant bone disease

The most commonly used positron emission tomography (PET) tracer in clinical practice, fluorine-18 fluorodeoxyglucose ( (18)F-FDG) is a glucose analogue that directly gains entry in excess into tumor cells. It is therefore sensitive for the detection of early bone marrow involvement prior to any identifiable bone changes. The introduction of (18)F-FDG-PET in the imaging algorithms of various malignant diseases often obviates the need to perform a separate assessment of malignant bone involvement with conventional bone scintigraphy. After therapy, disappearance of (18)F-FDG accumulation indicates success even when the bone remains morphologically abnormal. Novel hybrid systems composed of PET and computed tomography (CT) allow for acquisition of both modalities in the same clinical setting and the generation of fused functional-anatomical images. This technique has been found to improve the diagnostic accuracy of PET in detecting malignant bone involvement. This article discusses the role of PET/CT, primarily (18)F-FDG PET/CT, in the assessment of malignant bone involvement in patients with primary bone sarcomas, common solid malignancies, lymphoma, and multiple myeloma.     

Imaging gastric cancer with PET and the radiotracers 18F-FLT and 18F-FDG: a comparative analysis.

In this pilot study, we evaluated 3'-deoxy-3'-(18)F-fluorothymidine (FLT) PET for the detection of gastric cancer and compared the diagnostic accuracy with that of (18)F-FDG PET. METHODS: Forty-five patients (31 male and 14 female) with histologically proven locally advanced gastric cancer underwent attenuation-corrected whole-body (18)F-FLT PET and (18)F-FDG PET/CT (low-dose CT). (18)F-FLT emission images were acquired on a full-ring PET scanner 45 min after the injection of 270-340 MBq of (18)F-FLT. (18)F-FDG PET/CT was performed 60 min after the injection of 300-370 MBq of (18)F-FDG. Mean standardized uptake values for (18)F-FLT and (18)F-FDG were calculated using circular ROIs (diameter, 1.5 cm) in the primary tumor manifestation site, in a reference segment of the liver, and in the bone marrow and were compared on a lesion-by-lesion basis. RESULTS: According to the Lauren classification, 15 tumors (33%) were of the intestinal subtype and 30 (67%) of the nonintestinal subtype. (18)F-FLT PET images showed high contrast for the primary tumor and proliferating bone marrow. In all patients (45/45), focal (18)F-FLT uptake could be detected in the primary tumor. In contrast, 14 primary tumors were negative for (18)F-FDG uptake, with lesional (18)F-FDG uptake lower than or similar to background activity. The mean standardized uptake value for (18)F-FLT in malignant primaries was 6.0 +/- 2.5 (range, 2.4-12.7). In the subgroup of (18)F-FDG-positive patients, the mean value for (18)F-FDG was 8.4 +/- 4.1 (range, 3.8/19.0), versus 6.8 +/- 2.6 for (18)F-FLT (Wilcoxon test: P = 0.03). Comparison of mean (18)F-FLT and (18)F-FDG uptake in tumors with signet ring cells revealed no statistically significant difference between the tracers (6.2 +/- 2.1 for (18)F-FLT vs. 6.4 +/- 2.8 for (18)F-FDG; Wilcoxon test: P = 0.94). CONCLUSION: The results of this study indicate that imaging gastric cancer with the proliferation marker (18)F-FLT is feasible. (18)F-FLT PET was more sensitive than (18)F-FDG PET, especially in tumors frequently presenting without or with low (18)F-FDG uptake, and may improve early evaluation of response to neoadjuvant treatment.     

The role of (18)F-FDG PET/CT in initial staging of patients with locally advanced breast carcinoma with an emphasis on M staging

Locally advanced breast cancer (LABC) is a distinct entity in breast carcinoma with high incidence of distant metastases (M). However, there is scarce data in the literature addressing the role of fluorine-18-fluorodeoxyglucose-positron emission tomography/computed tomography ((18)F-FDG PET/CT) in LABC. This study was performed to assess the sensitivity of (18)F-FDG PET/CT in confirming known lymph nodal and M and in identifying new ones in LABC. We performed a retrospective analysis of data of 16 patients with LABC who underwent histopathology, for the diagnosis of LABC and clinical examination, chest X-rays, ultrasound of the abdomen and whole body bone scans. Findings for M obtained by all the above examinations were compared to the (18)F-FDG PET/CT findings that followed. Lymph nodal and distant metastases detected by all other examinations were detected by (18)F-FDG PET/CT in all patients, except subcentimetric metastases in 2 patients in the axilla that were detected in another examination later. Additionally, (18)F-FDG PET/CT identified unknown ipsilateral, supraclavicular, internal mammary metastases and upstaged disease in 3 patients and additional distant metastases were noted in 3/16 patients. In conclusion, our study suggests that more extra axillary lymph nodal and distant metastases can be identified by (18)F-FDG PET/CT as compared to a group of clinical, X-rays, ultrasound and bone scan examinations together.     

Comparison of diagnostic ability between 99mTc-MDP bone scan and 18F-FDG PET/CT for bone metastasis in patients with small cell lung cancer

Objective

The aim of this study was to compare the diagnostic ability of ¹⁸F-fluorodeoxyglucose (¹⁸F-FDG) positron emission tomography/computed tomography (PET/CT) with that of ^99mTc-methylene diphosphonate (^99mTc-MDP) bone scan for bone metastasis in staging patients with small cell lung cancer (SCLC).

Methods

Ninety-five patients with SCLC who underwent both ¹⁸F-FDG PET/CT and ^99mTc-MDP bone scan for initial staging work-up were retrospectively enrolled. All ¹⁸F-FDG PET/CT and bone scan images were visually assessed. Bone metastasis was confirmed by histopathological results and all available clinical information.

Results

Of 95 patients with SCLC, metastatic bone lesions were found in 30 patients, and 84 metastatic lesions were evaluated on a lesion-basis analysis. The sensitivity of ¹⁸F-FDG PET/CT was 100?% on a per-patient basis and 87?% on a per-lesion basis, and there was no false-positive lesion on PET/CT images. In contrast, the sensitivity of the bone scan was 37?% on a per-patient basis and 29?% on a per-lesion basis. The bone scan showed 11 false-positive lesions. The bone scan detected two metastatic lesions that were not detected by PET/CT, which were outside the region scanned by PET/CT. On follow-up bone scan, 21 lesions that were not detected by the initial bone scan but were detected by PET/CT were newly detected.

Conclusions

In patients with SCLC, ¹⁸F-FDG PET/CT showed higher detection rate of bone metastasis than ^99mTc-MDP bone scan. Thus, ¹⁸F-FDG PET/CT can replace bone scan in staging patients with SCLC.     

Increased (18)F-fluorodeoxyglucose uptake in benign, nonphysiologic lesions found on whole-body positron emission tomography/computed tomography (PET/CT): accumulated data from four years of experience with PET/CT

The use of (18)F-fluorodeoxyglucose positron emission tomography ((18)F-FDG-PET) in the field of oncology is rapidly evolving; however, (18)F-FDG is not tumor specific. Aside from physiological uptake (18)F-FDG also may accumulate in benign processes. Knowledge of these (18)F-FDG-avid nonmalignant lesions is essential for accurate PET interpretation in oncologic patients to avoid a false-positive interpretation. Through the systematic review of the reports of PET/computed tomography (CT) studies performed in oncologic patients during a 6-month period, we found benign nonphysiological uptake of (18)F-FDG in more than 25% of studies. In half of these, (18)F-FDG uptake was moderate or marked in intensity, similar to that of malignant sites. A total of 73% of benign lesions were inflammatory in nature, with post-traumatic bone and soft-tissue abnormalities (including iatrogenic injury) and benign tumors accounting for the remainder. The differentiation of benign from malignant uptake of (18)F-FDG on PET alone may be particularly challenging as a result of the low anatomical resolution of PET and paucity of anatomical landmarks. Fusion imaging, namely PET/CT, has been shown to improve not only the sensitivity of PET interpretation but also its specificity. Aside from better anatomical localization of lesions on PET/CT, morphological characterization of lesions on CT often may improve the diagnostic accuracy of nonspecific (18)F-FDG uptake. Correlation with CT on fused PET/CT data may obviate the need for further evaluation or biopsy in more than one-third of scintigraphic equivocal lesions. Familiarity with (18)F-FDG-avid nonmalignant lesions also may extend the use of (18)F-FDG-PET imaging beyond the field of oncology. We have tabulated our experience with benign entities associated with increased (18)F-FDG uptake on whole-body PET/CT from 12,000 whole-body (18)F-FDG-PET/CT studies performed during a 4-year period.     

18F-FDG PET/CT in suspected recurrences of epithelial malignant pleural mesothelioma in asbestos-fibers-exposed patients (comparison to standard diagnostic follow-up)

This retrospective study evaluated the role of 18-fluorine-labeled 2-deoxy-2-fluoro-d-glucose positron emission tomography/computed tomography (18F-FDG PET/CT) in patients with previous occupational or environmental exposure to asbestos, with histopathological diagnosis of epithelial malignant pleural mesothelioma and suspected recurrences, comparing the data from 18F-FDG PET/CT and computed tomography with contrast enhancement (CECT). 18F-FDG PET/CT has greater sensitivity than CECT in identifying local extent, lymph nodes, and metastasis. 18F-FDG PET/CT whole-body explorations are useful to monitor the follow-up and evaluate the metabolic response to chemo- and radiotherapy, modifying the scheduled treatment plan.     

Squamous papilloma of the oral cavity and oropharynx on 18F-FDG PET/CT imaging

Squamous papilloma is one of the most common benign neoplasms of the oral cavity and oropharynx. The (18)F-FDG PET/CT metabolic phenotype of this entity has not been described. We document the incidental finding of a hypermetabolic lesion at the right base of the tongue on an FDG PET/CT that proved to be squamous papilloma. The maximum standard uptake value was high at 7.0 g/ml. We conclude that oral cavity squamous papilloma can present with an intensely hypermetabolic phenotype on (18)F- FDG PET/CT. This benign entity should be included in the differential diagnosis of FDG-positive oral and oropharyngeal lesions.     

Usefulness of Respiratory-Gated <Superscript>18</Superscript>F-FDG PET/CT in Detecting Upper Abdominal Fever Focus

Respiratory-gated ¹⁸F-fluorodeoxygluocse (¹⁸F-FDG) PET/CT has been successfully used to better localize malignancies in the lung or upper abdominal organs. However, clinical usefulness of respiratory-gated ¹⁸F-FDG PET/CT in detection of fever focus has not been reported yet. A 68-year-old male patient with a history of living donor liver transplantation and biliary stenting was referred for ¹⁸F-FDG PET/CT due to fever of unknown origin (FUO). To find the accurate fever focus, respiratory-gated and non-gated ¹⁸F-FDG PET/CT was performed. Respiratory-gated PET/CT readily revealed prominent hypermetabolic lesion in the distal common bile duct (CBD) area where previous surgical graft was in situ. Maximum standardized uptake value (SUVmax) and SUV ratio (SUR) were greater in the gated PET/CT (SUVmax 5.4 and SUR 3.5) than in the non-gated PET/CT (SUVmax 4.6 and SUR 3.0). Fever dramatically subsided after removal of the graft in the CBD. This case report implies that respiratory-gated ¹⁸F-FDG PET/CT can visualize upper abdominal fever focus with better contrast than the conventional non-gated method.     

Primary Renal Leiomyosarcoma Presenting with Subcutaneous and Osseous Metastases: Staging and Follow-Up with 18F-FDG PET/CT

A 60 year old woman who presented with multiple small subcutaneous nodules in the upper back and arms, was referred for an [18F] fluoro-2-deoxy-D-glucose (¹⁸F-FDG) positron emission tomography/computed tomography (PET/CT) after histological evaluation revealed metastatic leiomyosarcoma of unknown origin. The PET/CT showed multiple ¹⁸F-FDG-avid subcutaneous nodules, bone lesions, as well as a large left renal mass, which was biopsied to confirm a primary renal leiomyosarcoma arising from the renal parenchyma. A post therapy PET/CT showed overall progression of disease. The use of ¹⁸F-FDG PET/CT in the staging and evaluation of response to therapy of a renal leiomyosarcoma has not been previously described in the literature.     

Clinical significance of 18F-α-methyl tyrosine PET/CT for the detection of bone marrow invasion in patients with oral squamous cell carcinoma: comparison with 18F-FDG PET/CT and MRI

Objective

L-3-[¹⁸F]-fluoro-α-methyl tyrosine (¹⁸F-FAMT) is an amino acid tracer for positron emission tomography/computed tomography (PET/CT) which specifically transported into cancer cells by L-type amino acid transporter 1 (LAT1). LAT1 overexpression in tumors is significantly correlated with cell proliferation and angiogenesis. ¹⁸F-FAMT PET/CT, fluorine-18-fluorodeoxyglucose (¹⁸F-FDG) PET/CT and magnetic resonance imaging (MRI) were compared for their diagnostic performance in the detection of bone marrow invasion in patients with oral squamous cell carcinoma (OSCC).

Methods

Twenty-seven patients with OSCC on the upper or lower alveolar ridge underwent staging by MRI, ¹⁸F-FDG PET/CT and ¹⁸F-FAMT PET/CT studies before surgery. Post-surgical pathologic examination was used as the standard to determine the final diagnoses. The possibility of bone marrow invasion on MRI, ¹⁸F-FDG PET/CT and ¹⁸F-FAMT PET/CT were usually graded retrospectively into five-point score. Sensitivity, specificity, accuracy, positive predictive value (PPV) and negative predictive value (NPV) were calculated according to the obtained scores.

Results

As the sensitivity of ¹⁸F-FDG PET/CT was highest (100 %) among that of MRI (95 %) and ¹⁸F-FAMT PET/CT (90 %), the specificity of ¹⁸F-FAMT PET/CT was highest (85.7 %) among that of MRI (57 %) and ¹⁸F-FDG PET/CT (14.3 %). The size of pathological tumor was accorded with that detected by ¹⁸F-FAMT PET/CT and was smaller than that detected by ¹⁸F-FDG PET/CT (P < 0.01). Significant difference was not found between ¹⁸F-FAMT PET tumor volume and pathological tumor volume.

Conclusions

¹⁸F-FAMT PET/CT was useful and more specific than MRI or ¹⁸F-FDG PET/CT in the detection of bone marrow invasion of OSCC and may contribute to minimize the extent of resection in oral surgery patient.     

A seldom case of primary urethral malignant melanoma and breast cancer detected by (18)F-FDG PET/CT

In the 1(st )issue of HJNM for 2012 we read with interest a case where 3 different cancers were detected. Synchronous second malignancy can be incidentally detected in routine fluorine-18-fluoro-deoxy-glucose positron emission tomography/computed tomography ( (18)F-FDG PET/CT) imaging in approximately 1% of cancer patients with lungs being the most frequent site. We report the (18)F-FDG PET/CT scan for staging of the primary malignant melanoma of the urethra and for the detection of another malignancy in the breast in the same patient, since primary malignant melanoma of urethra is very seldom. A 65 years old post-menopausal woman presented with increased frequency of micturition, dysuria and a gradually enlarging mass protruding from the external urethral meatus. Fine needle aspiration cytology (FNAC) performed from the mass revealed malignant melanoma. On cystourethrescopy examination, a 4x4 cm blackish mass was noted at the external urethral meatus with a satellite nodule in the bladder trigone. Contrast enhanced CT (CeCT) of the pelvis showed soft tissue thickening along the urethra infiltrating urinary bladder neck and vagina. Analysis of (18)F-FDG PET/CeCT was performed to assess the extent of the disease. Intensely (18)F-FDG avid soft tissue mass (SUV(max): 20.1) was noticed along the entire length of the urethra with hypermetabolic right inguinal and left external iliac lymph nodes. In addition to (18)F-FDG uptake in the bladder wall and the vaginal wall, intense (18)F-FDG uptake was also seen in two soft tissue nodules in the right breast and in the axillary lymph nodes suggestive of a second primary in the breast. Cytological diagnosis of intraductal breast carcinoma was made after FNAC from the breast nodule. Urethral melanoma was treated with anterior exenteration and ileal conduit. Histopathology confirmed the diagnosis of primary malignant melanoma of urethra infiltrating the urinary bladder and anterior vaginal wall. Postoperative histopathology from the right inguinal and left external iliac lymph nodes revealed metastatic disease. The diagnostic contribution of PET/CT was crucial. Melanotic melanoma cells have a distinctive MRI signal, which may be helpful in diagnosis. In this case whole body MRI could have been of equal value for accurate staging of urethral melanoma, but whole body MRI is a cumbersome procedure and often is not practical. Primary urethral carcinoma is very rare and an annual ageadjusted incidence rate of 4.3 per 106 in males and 1.5 per 106 in females has been reported in USA. Primary malignant melanoma of the urethra is rare, representing less than 1% of all melanomas and 4% of urethral cancers. Furthermore, the incidence of two primary cancers is rare and is reported to be between 0.3% and 4.3%. Primary malignant melanoma of the urethra has a worse prognosis than its cutaneous counterpart, partly due to delayed diagnosis. At the time of diagnosis, urethral melanoma is usually deeply invasive and locally extended to the vagina or vulva or the corpora cavernosa. Inguinal lymph node metastases are present at diagnosis in half of the cases and distant metastases in one third of them. Positron emission tomography demonstrates specificity and accuracy of 94.7% and 73% respectively in detecting lymph nodal metastases. Sensitivity, specificity and accuracy of (18)F-FDG PET/CT in detecting metastases in high risk patients were 85%, 96%, 91% while for (18)F-FDG PET/CT with dedicated CT interpretation were 98%, % and 96%, respectively. Recently, the role of (18)F-FDG PET/CT in treatment response evaluation of melanoma patients has also been demonstrated. Incidental (18)F-FDG uptake in the breasts is rare, and the lesion may be malignant in up to 57% of the cases. To our knowledge no published literature is available on synchronous breast carcinoma and urethral melanoma. The reason why some patients are more prone to develop multiple cancers remains obscure. One possibility may be of a genetic predisposition linking the two cancers. Research suggests that mutations in CDKN2A, a gene that indicates high risk of developing melanoma, also puts carriers at an up to 3.8 times greater risk of breast cancer. Similarly, mutations in the gene of breast cancer susceptibility, BRCA2, increase carriers' risk of melanoma by as much as 2.58 times. In conclusion, we describe a case of two primary carcinomas: a unique urethral malignant melanoma and a breast carcinoma, detected and staged by (18)F-FDG PET/CT.     

Characterizing IgG4-related disease with 18F-FDG PET/CT: a prospective cohort study

Purpose

IgG4-related disease (IgG4-RD) is an increasingly recognized clinicopathological disorder with immune-mediated inflammatory lesions mimicking malignancies. A cohort study was prospectively designed to investigate the value of ¹⁸F-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) in characterizing IgG4-RD.

Methods

Thirty-five patients diagnosed with IgG4-RD according to the consensus criteria were enrolled with informed consent. All patients underwent baseline ¹⁸F-FDG PET/CT evaluation. Among them, 29 patients underwent a second ¹⁸F-FDG PET/CT scan after 2 to 4 weeks of steroid-based therapy.

Results

All 35 patients were found with ¹⁸F-FDG-avid hypermetabolic lesion(s); 97.1 % (34/35) of these patients showed multi-organ involvement. Among the 35 patients, 71.4 % (25/35) patients were found with more organ involvement on ¹⁸F-FDG PET/CT than conventional evaluations including physical examination, ultrasonography, and computed tomography (CT). ¹⁸F-FDG PET/CT demonstrated specific image characteristics and pattern of IgG4-RD, including diffusely elevated ¹⁸F-FDG uptake in the pancreas and salivary glands, patchy lesions in the retroperitoneal region and vascular wall, and multi-organ involvement that cannot be interpreted as metastasis. Comprehensive understanding of all involvement aided the biopsy-site selection in seven patients and the recanalization of ureteral obstruction in five patients. After 2 to 4 weeks of steroid-based therapy at 40 mg to 50 mg prednisone per day, 72.4 % (21/29) of the patients showed complete remission, whereas the others exhibited > 81.8 % decrease in ¹⁸F-FDG uptake.

Conclusion

F-FDG PET/CT is a useful tool for assessing organ involvement, monitoring therapeutic response, and guiding interventional treatment of IgG4-RD. The image pattern is suggested to be updated into the consensus diagnostic criteria for IgG4-RD.