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Myxofibrosarcoma is a malignant fibroblastic soft tissue neoplasm containing a variable amount of myxoid stroma that commonly presents as a slow-growing mass in elderly patients. The neoplasm may be superficial or deep to the muscle fascia and characteristically has an infiltrative growth pattern with a dominant or multinodular mass. We describe an unusual case of high-grade myxofibrosarcoma of the wrist and forearm that infiltrated the muscles, tendons, and wrist joint, causing bone erosions. The tumor was mistakenly diagnosed as synovitis and a chronic, erosive, inflammatory process. The diffuse nature, absence of a dominant mass, and radiographic appearance complicated the diagnosis. Although neoplasms of the synovial spaces are rare, this case demonstrates that tumors with a highly infiltrative growth pattern can mimic inflammatory synovitis and that neoplasms should be considered in the differential diagnosis when clinical and laboratory features are discordant with the imaging appearance.

Objective: To describe our experience of the magnetic resonance imaging (MRI) appearances after hindquarter amputation, focusing on the normal pattern of time-related changes in signal intensity within the amputation flap and appearances of local disease recurrence., Materials and Methods: This was a retrospective review of the records of patients identified on our orthopaedic oncology database who had undergone hindquarter amputation at our centre. Examinations were divided into one group consisting of 'normal' postoperative findings and another group demonstrating local recurrence. 'Normal' postoperative findings were assessed for signal intensity, morphology and presence of the 'muscle texture sign' within the amputation flap. Examinations were grouped according to time from surgery. Examinations demonstrating local recurrence were assessed for site, signal intensity, morphology and axial dimensions of recurrent tumour. Comparison was made to pre-operative imaging., Results: Thirty-five patients with postoperative MR images were identified. Seventy-seven examinations were reviewed (range 1-18 per patient). The 'normal group' comprised 18 patients (seven female, 11 male, mean age 44 years, range 16-75 years), with 47 examinations reviewed. The 'muscle texture sign' was preserved in all examinations in this group. Up to 6 months after surgery, 100% (10) of examinations showed hyperintense T2- and short-tau inversion recovery (STIR-weighted) signals within the muscle flap, indicating oedema. Only after 4 years was the muscle flap signal isointense in all cases (13). Up to 6 months after surgery, 50% (5 of 10) of examinations demonstrated flap swelling, but after 1 year, 100% (28) showed atrophy. Twenty percent (2 of 10) of examinations 0-6 months from surgery showed hyperintense T1-weighted signal within the muscle flap, consistent with fatty infiltration, but after 2 years, 100% (20) showed a hyperintense T1-weighted signal. The 'local recurrence' group comprised 20 patients (six female, 14 male, mean age 45.7 years, range 14-69 years), with 30 examinations demonstrating recurrent disease or metastasis. There were 23 recurrent tumours, of which 43% (10) were in the muscle component of the amputation flap, 13% (3 of 23) were in subcutaneous tissues of the flap, 13% (3 of 23) were at the posterior margin of the bone resection and 13% (3 of 23) were paraspinal. All recurrent tumours demonstrated hyperintense T2 and STIR signals. The signal intensity pattern of recurrence closely followed that of the original tumour. The 'muscle texture sign' was absent in all examinations demonstrating recurrence in muscle flap., Conclusion: A pattern of time-related signal intensity and morphological changes is observed within normal hindquarter amputation flaps on MRI. Recurrent disease is most likely to occur within the muscle flap, typically of high T2-weighted signal intensity and characteristically follows the signal pattern of the original tumour.

Objective: The objective of this study is to describe the imaging features of non-neoplastic masses suspected of being tumor recurrences adjacent to allografts. The allografts were utilized for the treatment of various musculoskeletal tumors., Materials and Methods: We reviewed the medical records and imaging studies of 56 patients who were suspected of having recurrent tumors following surgical resection and allograft replacement treatment for a variety of musculoskeletal neoplasms. The imaging modalities included radiographs, CT, and MRI., Results: There were 47 cases of recurrent tumors. All tumor recurrences were in the soft tissues of the surgical bed (41 patients), or in the native bone adjacent to the host/allograft junction (6 patients). None of the recurrences originated in the allografts. Nine patients suspected of having recurrences were discovered to have non-neoplastic masses. Five of these were very closely related to the allograft, wrapping around parts of the allograft, and the other 4 were in the surgical bed, 2 of which were abscesses and two were seromas., Conclusion: Most masses arising in the vicinity of allografts implanted following resection of musculoskeletal tumors represent recurrent neoplasms. A minority are reactive processes or abscesses or fluid collections. These "pseudoneoplasms," specifically those closely related to the allografts, have specific imaging characteristics that help distinguish them from recurrent tumors.

The rare coexistence of intramuscular myxoma (IM) and fibrous dysplasia (FD) is known as Mazabraud's syndrome. IM tends to occur multifocally and is associated most frequently with polyostotic FD in Mazabraud's syndrome. We present an extremely rare combination of a solitary IM and monostotic FD as a variant of Mazabraud's syndrome, and discuss the importance of recognizing this rare coexistence for appropriate management of the patient.

Diffuse-type giant cell tumor (D-TGCT) is known as a synonym for pigmented villonodular synovitis (PVS), a condition usually found in the large joints. We report an extremely rare case of D-TGCT which was located within the hamstring muscle. The lesion was an incidental finding in a 62-year-old man who underwent positron emission tomography (PET) as part of a staging evaluation for gastric cancer. The lesion was resected. There has been neither metastasis nor recurrence during the 6-month period since resection. This case demonstrates that PVS/D-TGCT may have a high SUV on PET imaging, and for this reason PET may be useful for detecting both the tumor and any recurrence.

Objective: The purpose of this study was to clarify the usefulness of MR imaging for preoperative diagnosis and evaluation of the extent of localized giant cell tumor of tendon sheath (GCTTS)., Design and Patients: We retrospectively reviewed the MR images of 25 patients with surgically proved GCTTS (seven males and 18 females; mean age, 41 years) including five recurrences. T1- and T2-weighted imaging was carried out on 24 and 22 lesions, respectively. Gadolinium-enhanced images were obtained for 20 lesions. We evaluated the tumor extent around the phalanx (the degree of circumferential occupation by a tumor around the phalanx on an axial plane) and involvement of the bone, joint, and tenosynovial space by both MR imaging and surgery (gold standard)., Results: MR signal intensities of the GCTTSs were consistently equal to those of skeletal muscle or between those of muscle and fat on T1-weighted images; on T2-weighted images, the signal intensities tended to be between those of muscle and fat. Most lesions were inhomogeneous due to low-signal-intensity areas, and enhanced following gadolinium administration. The tumor extent around the phalanx was 168.5 +/- 99.2 degrees (63-360 degrees). MR imaging did not identify the bone involvement (five lesions), but depicted the involvement of the joint in four of five lesions and the tenosynovial space in nine of ten lesions., Conclusions: This study confirms that MR imaging is able to depict the characteristic internal signal of GCTTS. Moreover, it can accurately assess the tumor size and degree of extent around the phalanx, which can affect the type of surgical approach.

This case report describes the features of gadolinium-enhanced MRI in well-differentiated liposarcoma with histologic correlation and addresses the usefulness of this imaging technique in distinguishing well-differentiated liposarcoma from lipoma. Gadolinium-enhanced MRI revealed significantly enhanced signal in well-differentiated liposarcoma in a background of multiple well-differentiated benign fatty masses by showing the increased vascularity in the septa of well-differentiated liposarcoma. Although such signal enhancement can be seen in some types of benign lipomatous tumors with increased blood vessels, this technique is helpful in selection of biopsy site, especially in a clinical setting of multiple fatty masses.

Spindle cell hemangioendothelioma occurring in skeletal muscle is extremely rare. No reported studies have performed an imaging evaluation of intramuscular spindle cell hemangioendothelioma. We report on such a tumor arising in an unusual site, the right extensor digiti minimi, in a 46-year-old woman. An en bloc resection was performed and the patient has been disease free for 8 years. Radiologic imaging in the present case showed similar findings to those described in intramuscular hemangioma.

Merkel cell carcinoma is a rare highly malignant tumour. There have been previous descriptions of the CT appearances of this tumour, but to our knowledge this is the first MRI description. MRI may be a more sensitive method of initial evaluation of the local extension of the primary tumour.

We describe a malignant granular cell tumor in the semimembranosus muscle of a 61-year-old woman. Magnetic resonance images disclosed a tumor with intermediate and low signal intensity on both T1- and T2-weighted images, measuring about 7 x 4 x 4 cm in size. The patient showed an uneventful clinical course during a 30-month follow-up period after the wide excision. The pertinent findings in making the diagnosis of malignant granular cell tumor are large size, intramuscular location, and mitosis including an atypical mitosis.