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45 岁男性髋关节原发性滑膜软骨肉瘤:病例报告及文献复习。

Primary synovial chondrosarcoma of the hip joint in a 45-year-old male: case report and literature review.

机构信息

Department of Radiology, NYU Hospital for Joint Diseases, 301 E 17th Street, New York, NY 10003, USA.

出版信息

Skeletal Radiol. 2011 Oct;40(10):1375-81. doi: 10.1007/s00256-011-1172-9. Epub 2011 May 12.

Abstract

Synovial chondrosarcoma is a rare tumor, seen most commonly arising from antecedent synovial chondromatosis, the more common benign entity. The distinction between the two can be difficult on the basis of clinical, imaging, and histologic criteria. The authors report a case of pathologically proven synovial chondrosarcoma of the hip in a 45-year-old male initially treated for presumed synovial chondromatosis. The case is made more unusual by the fact that no evidence of co-existent synovial chondromatosis was noted at histology. The literature as regards synovial chondrosarcoma, both de novo and secondary cases, is reviewed.

摘要

滑膜软骨肉瘤是一种罕见的肿瘤,最常见于先前存在的滑膜软骨瘤病,这是一种更常见的良性实体。这两种疾病在临床、影像学和组织学标准的基础上很难区分。作者报告了一例经病理证实的髋关节滑膜软骨肉瘤病例,患者为 45 岁男性,最初被诊断为疑似滑膜软骨瘤病。该病例更为罕见的是,组织学检查未发现同时存在滑膜软骨瘤病的证据。对滑膜软骨肉瘤(包括原发性和继发性病例)的文献进行了回顾。

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