Scintigraphic patterns in osteoid osteoma and spondylolysis

A retrospective review was performed of radionuclide bone scans and radiographs of 54 children with diagnoses of spondylolysis or osteoid osteoma/osteoblastoma. The findings indicate that skeletal scintigraphy shows imaging patterns that can be used to help distinguish these two conditions. Most cases of spondylolysis and all cases of osteoid osteoma or osteoblastoma demonstrated focally increased activity on the delayed skeletal scintigrams. Evaluation of the bone scan images obtained during the immediate postinjection period revealed intense activity with osteoid osteoma and osteoblastoma, but minimal or no abnormal activity in cases of spondylolysis. In addition, spondylolysis was the only condition that produced bilateral abnormalities in the pars interarticularis region in these children.     

Osteoid osteoma and osteoblastoma of the talus

Forty patients with osteoid osteoma or osteoblastoma of the talus are presented. Clinical and radiographic findings, histologic features, and therapy of these lesions are discussed. The body of the talus was involved in two patients, all other lesions being located in the neck of the bone. Subperiosteal lesions accounted for 75% of cases, and medullary lesions for 25%. Thirty of the 40 lesions were paraarticular. Five radiographic appearances in the talus are discussed: subperiosteal target lesions of the neck (54%); medullary lesions of the neck (20%); subperiosteal radiolucent lesions of the neck (13%); medullary lesions of the body (5%); and exostotic osteoid osteoma of the talar neck (3%).Supported by Grant No. 85.02793.44, Special Project Oncology, Italian National Council of Researchers     

Osteoid osteoma in cancellous bone.

Osteoid osteoma in cancellous bone lacks the usual osteoblastic reaction that accompanies the classical cortical or juxtacortical osteoid osteoma. Familiarity with this type of presentation should instigate the appropriate diagnostic steps, including nuclear medicine studies using pin-hole collimation, and thin tomographic cuts.     

Osteoblastomatosis of bone. A benign,multifocal osteoblastic lesion,distinct from osteoid osteoma and osteoblastoma,radiologically simulating a vascular tumor

Two adult patients are described with multifocal osteolytic lesions radiologically simulating a vascular tumor. One patient had multiple bones involved. Histologically, the individual lesions had the features of the nidus of osteoid osteoma/osteoblastoma. A review of the English language medical literature yielded only one other reported case with similar features. The process is designated as osteoblastomatosis to indicate its bone-forming character, prominent osteoblast proliferation, and multiplicity. The cases are distinguished from multifocal/multicentric osteoid osteoma and osteoblastoma, and from benign and malignant vascular tumors. Presented at the International Skeletal Society Meeting, (M. Sundaram, Case 7), Toronto, Canada, 1993 (Case 1), and (G.Y. El-Khoury, Case 20) San Francisco, 2003 (Case 2).     

Osteoid osteoma and osteoblastoma of the vertebrae

Five cases of osteoid osteoma and five cases of osteoblastoma of the spine are reported. All the patients underwent surgery and the radiographic diagnosis was always histologically confirmed. Conventional radiographic technique using tomography constantly permitted the diagnosis. Computed tomography was primarily useful for spatial localization of the lesion. The authors evaluate the radiographic findings of the two lesions discussing the symptoms which are suspected for these pathologic conditions. Bone scintigraphy must precede radiological examination.     

CT of osteoid osteoma of the femoral neck: the value of oblique reformatting

An osteoid osteoma is a benign bone lesion which may involve the femoral neck. The lesions are distinctively osteoblastic, containing a central fibrovascular and osteoid nidus which often evokes substantial periosteal reaction occasionally making the diagnosis by conventional radiography very difficult. Computed tomographic evaluation of these lesions at other sites has been previously reported. I wish to emphasize the unique value of CT multiplanar reformatting in a patient with an osteoid osteoma of the femoral neck.     

Osteoid osteoma: MR imaging revisited

To assess and compare with computed tomography (CT) the performance of magnetic resonance (MR) imaging in the detection of osteoid osteoma, and determine the features of this lesion on MR imaging. The prospective MR imaging and CT diagnosis of osteoid osteoma was determined from original radiology reports. MR images were assessed retrospectively with regard to the location and signal intensity of the nidus and surrounding bone marrow and soft tissue edema. These findings were correlated with the age of the patient, duration of symptoms, and drug therapy. Ten patients with histologically proven osteoid osteoma who underwent MR imaging were reviewed. All 10 lesions were correctly diagnosed at the time of MR imaging. None of the lesions was intracortical. Nine lesions were intra-articular. Two out of five patients with extracortical lesions had false negative CT preceding the MR study. Signal intensity of the nidus, marrow, and soft tissue edema on MR imaging were variable. Perinidal edema was most pronounced in younger patients and had no apparent relation to drug therapy. MR imaging reliably demonstrates the nidus of an osteoid osteoma, which has a variable appearance related to its position relative to the cortex of the bone. A predominance of cancellous osteoid osteomas are encountered in patients referred for MR imaging. Marrow edema in the vicinity of the lesion improves the conspicuity of the nidus. CT may fail to diagnose osteoid osteoma when the nidus is in a cancellous location, due to the lack of perinidal density alteration.     

Osteoid osteoma simulating osteomyelitis: Differentiation with Tc-99m HIG scintigraphy

We present a case of osteoid osteoma with a history of mild pain, local swelling and point tenderness on the right lower leg. The diagnosis of osteoid osteoma was difficult due to the atypical clinical history and misleading radiological and bone scan findings. When it is difficult to differentiate an osteoid osteoma from osteomyelitis using CT, MRI or bone scan; HIG scintigraphy can be used to exclude an infection.     

Osteoid osteoma of the second metatarsal bone diagnosed on MRI: A case report and literature review

Osteoid osteoma is a relatively common benign bone tumor that is most frequently seen on the appendicular skeleton in adolescents and young adults. Here we present the case of a 14-year-old boy presenting with a 10 month history of pain in his left foot which had been misdiagnosed as stress fracture due to its unusual clinical presentation. Magnetic resonance imaging of the left foot revealed a bone lesion with typical features of the osteoid osteoma on the distal part of the second metatarsal bone. The lesion was surgically removed and the diagnosis of osteoid osteoma was confirmed by post-surgical histopathologic examination of the resected section. The patient reported a substantial relief in his pain 4 weeks following the surgical operation.     

Discrete synchronous multifocal osteoid osteoma of the humerus

 A 24-year-old patient is described who had a 4-year history of pain in the right upper arm, with distinct night pain, that responded to salicylates. From the findings on conventional radiography, bone scintigraphy and MRI a multifocal osteoid osteoma was suspected, with one focus in the cancellous region of the greater tuberosity and a second cortical focus at the proximal humeral diaphysis. The resection ’’en bloc’’ of both tumors and histological examination confirmed the diagnosis. The patient was painfree after the curative resection of the two osteoid osteomas. Osteoid osteoma is a frequently found benign bone tumor, accounting for approximately 11% of cases. In rare cases a multicentric occurrence has been described. A possible occurrence of more than one osteoid osteoma in a single bone, not verified histologically, has been reported only three times in the literature. In patients with scintigraphic and radiographic findings of two foci, discrete synchronous multifocal osteoid osteomas should be suspected.     

Osteoid osteoma

Osteoid osteoma is a benign skeletal neoplasm composed of osteoid and woven bone that rarely exceeds 1.5 cm in greatest dimension. The lesion is most commonly located in the cortex of long bones where it is associated with dense, fusiform, reactive sclerosis. Less often, it may be cancellous, where reactive osteosclerosis is usually less intense and may be distant from the lesion. Cancellous lesions are frequently intraarticular (most often in the hip) and may be associated with synovitis and joint effusion. Rarely, osteoid osteomas occur in a subperiosteal location. Patients are usually young, and there is a strong male predominance. Pain is the most common symptom. Radiographs of patients with cortical osteoid osteoma are often diagnostic. Intraarticular lesions, however, may be subtle, and scintigraphy may be required to locate the lesion for subsequent computed tomography (CT). CT is useful to identify and precisely locate the lesion and to provide guidance for percutaneous localization or treatment.     

Osteoid osteoma of the elbow

Six cases of osteoid osteoma of the elbow were reviewed to determine the spectrum of clinical, pathologic and radiologic findings. Since osteoid osteoma of the elbow may masquerade as a nonspecific synovitis, the diagnosis is challenging and frequently delayed. The histology is, however, indistinguishable from that of osteoid osteoma occurring in typical locations. The radiologic features of osteoid osteoma of the elbow include the following triad: (a) osteosclerosis, usually a dominant feature at initial imaging and typically enveloping the nidus; (b) joint effusion; and (c) periosteal reaction that can involve both the bone in which the osteoid osteoma arises and adjacent bones. Awareness of these features will facilitate correct diagnosis, thereby facilitating timely and appropriate treatment.The opinions and assertions contained herein are the private views of the authors and are not to be construed as official or as reflecting the views of the Department of the Army, the Department of Defense or the Uniformed Services University of the Health Sciences     

Bone scintigraphy as a guide to the diagnosis of osteoid osteoma.

This report describes one case in which bone scintigraphy was helpful in establishing the diagnosis of osteoid osteoma and presents three other cases in which increased accumulation of 99mmTc-EHDP was found at the side of the osteoid osteoma. The study contributes to the observation by others that the osteoid osteoma occurs as a scintigraphic 'hotspot'. It is concluded that the diagnostic delay of the osteoid osteoma can be shortened when bone scintigraphy is performed more often and at an earlier stage in patients with unexplained bone pain or with a clinical history that leads to the suspicion of the presence of an osteoid osteoma.     

Osteoid osteoma. Distant, periarticular, and subarticular lesions as a cause of knee pain

Osteoid osteoma, a benign osteoblastic tumour comprised of osteoid and atypical bone, is a well-known entity. However, clinical diagnosis may be delayed, especially when the pain is referred to a nearby joint. This paper reports a series of 11 cases occurring in physically active patients in whom the diagnosis was delayed because of pain referral to the knee. The mean duration from the onset of symptoms to diagnosis of osteoid osteoma was 20 months (range 3 to 48 months). Review of these 11 lesions indicates that they can be classified on the basis of their anatomical location: (a) distant to the knee; (b) periarticular; or (c) subarticular (intraarticular). It should be noted that initially only 5 of the 11 cases displayed characteristic x-ray findings; in the remaining 6 cases, diagnosis was dependent on positive 99mTc radionuclide bone scans, tomograms, and computerised tomography scans. Of the 9 patients who underwent surgical resection of their lesions, all had complete relief of symptoms and all continued to be asymptomatic at follow-up evaluations.     

Osteoid osteoma mimicking chronic arthritis. Diagnosis by bone scintigraphy

The case of a patient with osteoid osteoma of the heel is presented. The patient was misdiagnosed and treated for four years as having arthritis. Osteoid osteoma was diagnosed by 99mTc-MDP bone scan that was performed for the evaluation of the arthritis. Plain radiography and magnetic resonance imaging (MRI) were negative for signs of arthritis. However, MRI when reevaluated after positive bone scintigraphy, was found positive for osteoid osteoma. This case underscores the value of bone scintigraphy for the diagnosis of osteoid osteoma.     

骨样骨瘤的影像诊断

目的评价平片、CT,MRI对骨样骨瘤的诊断价值.方法18例骨样骨瘤均摄平片,其中16例经CT检查,4例行MRI检查;分析骨样骨瘤的平片、CT,MBI影像学表现.结果骨样骨瘤典型表现为瘤巢及周围反应性骨质硬化,且随病变部位不同而有所差异.诊断准确性平片为92.9%,CT为100%,MRI为83.3%.结论平片是诊断骨样骨瘤的基本手段,CT为最可靠方法,MRI需结合平片、CT进行诊断.     

Benign bone tumors and tumor-like lesions: value of cross-sectional imaging

This article reviews the role of CT and MR imaging in the diagnosis of benign bone tumors and tumor-like lesions of bone with with regard to differential diagnosis, the assessment of tumor-related complications, and the detection of postoperative recurrence. Indications for cross-sectional imaging of specific lesions, including osteoid osteoma, osteoblastoma, enchondroma, osteochondroma, intraosseous lipoma, hemangioma, giant cell tumor, aneurysmal bone cyst, simple bone cyst, and eosinophilic granuloma, are discussed, and advantages and disadvantages of the different imaging modalities are illustrated on the basis of pathologically confirmed cases.     

骨样骨瘤的影像学诊断

目的 分析骨样骨瘤的X线、CT和MRI表现。方法 搜集经手术病理证实的骨样骨瘤48例，其中男33例，女15例。所有病例均行X线检查，其中同时行CT检查者32例，行MR检查者10例，3种检查方法都进行者8例。分析骨样骨瘤在X线、CT和MRI上的表现及其对瘤巢和瘤巢周围改变的显示能力。结果 48例病灶均表现为一圆形或卵圆形的透亮区，直径为0．4～1．7cm，平均9．7cm，其周围有不同程度的骨质硬化。10例行MR检查者均可见瘤巢周围的软组织、骨髓水肿或关节腔积液。48例X线平片仅37例显示瘤巢，32例行CT检查者均清楚显示瘤巢，X线和CT对瘤巢显示率分别为77％(37／48)和100％(32／32)。10例MR检查者均可作出正确诊断，其中8例能直接判断出瘤巢，另2例需对照平片或CT才能肯定。结论 瘤巢是确诊骨样骨瘤的关键，X线平片仍然是诊断骨样骨瘤的重要检查方法，CT是显示瘤巢的最佳方法，MRI能敏感地显示瘤巢周围骨髓内及软组织的炎性水肿，但可能造成误诊，结合平片或CT可作出准确诊断。     

99Tc^m-MDP骨显像评估脊柱骨样骨瘤及成骨细胞瘤射频消融效果

目的探讨99Tcm-亚甲基二磷酸盐骨显像对脊柱骨样骨瘤和成骨细胞瘤射频消融疗效评估的价值。资料与方法回顾性收集行射频消融的7例脊柱骨样骨瘤及成骨细胞瘤患者的影像学及临床资料,分析骨显像、CT表现与患者症状、随访结果的关系。结果7例患者(其中骨样骨瘤4例,成骨细胞瘤3例)接受8次射频消融。治疗后2例无疼痛复发,第3、6个月骨显像呈轻度浓聚,其中1例第3个月CT示病变缩小,第12个月消失。3例第4~5个月疼痛复发,骨显像呈轻度浓聚1例,显著浓聚2例,同期CT示病变较治疗前均无变化,继续随访患者疼痛消失。2例射频消融后仍有间断轻度疼痛,第9、12个月骨显像均呈显著浓聚,同期CT示病变缩小1例,增大1例,患者后续分别行手术和再次射频消融。结论骨显像能够早期判断骨样骨瘤和成骨细胞瘤射频消融后病变的活性。骨显像轻度浓聚预示病变治愈,显著浓聚提示病变尚存活性,需继续随访。     

Osteoid osteoma: operative confirmation of complete removal by bone scintigraphy

The high sensitivity of bone scintigraphy in detecting osteoid osteoma throughout the skeleton has been documented. Recently, radioactive surgical specimens of osteoid osteomas were studied with microradiography, autoradiography, and well-counter scintimetry and were shown to concentrate most of the radionuclide within the nidus of the lesion. These techniques also proved helpful to surgeons in achieving cure with conservative bone excision. We present two cases of osteoid osteoma, one of them recurrent, in which the patients were injected with bone-seeking agent just prior to surgery. The excised specimens were immediately imaged and the entire nidus was seen, confirming the complete removal of the lesion. This simple and rapid procedure is suggested whenever difficulty is anticipated in removal of an osteoid osteoma.