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EN
Posterior ankle impingement syndrome represents an important cause of chronic ankle pain and has been extensively described in the orthopaedic and radiology literature. A rare case of this painful hindfoot disorder that resulted from two concurrent developmental anomalies is presented herein.
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Bilateral lipoma arborescens of the knee: a case report

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EN
Lipoma arborescens, a diffuse articular lipomatosis, is a rare disorder characterized by marked villiform synovial proliferation and diffuse replacement of the subsynovial tissue by mature adipocytes. Unilateral joint involvement is the usual presentation while bilateral joint involvement is more uncommon. We reported a case of bilateral lipoma arborescens in a male patient with associated marked patellofemoral osteoarthritis and described the MR imaging findings.
EN
Step aerobics is one of the most popular exercises with established benefits to cardiovascular status. This activity is associated with injuries which include patellar or talar chondral lesions, quadriceps tendinopathy, Achilles tendinopathy or tear, shin splints and muscle soreness. The purpose of this case report is to present two step aerobics athletes, suffering from anterior knee pain. We observed that their knee MR examination disclosed only suprapatellar fat pad edema. No other findings were noticed. In addition, we discuss the possible pathogenetic mechanism of this entity which has not been previously reported in the literature.
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EN
Primary malignant vascular bone tumors are unusual and include hemangioendothelioma, epitheloid hemangioendothelioma and angiosarcoma. Although few cases of primary bone angiosarcomas have been reported, those of femoral origin are even more infrequent. Such tumors diagnosis may be challenging due to their radiographic and histologic variety. We present a case of a 24-yearold woman with a subperiosteal diaphyseal angiosarcoma originating from the femoral bone and metastatic to the lung at the time of diagnosis. The clinical, histological and radiological features of this extremely rare lesion are presented.
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