Malignant transformation of synovial chondromatosis into chondrosarcoma is unusual. Thirteen cases and one series have been reported; only four of them developed in the hip. The overall survival is about 50%, possibly because of the difficulty of arriving at a correct early diagnosis (radiographically and histologically) and subsequent adequate surgical therapy. We report two patients (ages 30 and 50 years) in whom synovial chondrosarcoma developed in previously excised synovial chondromatosis of the hip. The diagnosis was made with modern imaging techniques (computed tomography and magnetic resonance imaging) and verified by open biopsy. The early recognition allowed a wide limb-saving resection; both patients are disease free 3 and 2 years after surgery.

译文

:滑膜软骨瘤恶变为软骨肉瘤是罕见的。报告了13例和一系列病例;其中只有四个在臀部发育。总体存活率约为50%,这可能是由于难以进行正确的早期诊断(影像学和组织学)以及随后进行适当的手术治疗所致。我们报告了两名患者(年龄分别为30岁和50岁),其中滑膜软骨肉瘤在先前切除的髋关节滑膜软骨病中发展。诊断是使用现代成像技术(计算机断层扫描和磁共振成像)进行的,并通过开放式活检进行了验证。尽早发现,可以广泛地节省肢体。两名患者均在手术后3年和2年内无病。

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