Primary rhabdomyosarcoma of the distal femoral diaphysis: a case report and review of the literature

被引:6
|
作者
Bressner, Jarred A. [1 ]
McCarthy, Edward F. [2 ]
Fayad, Laura M. [3 ]
Morris, Carol D. [4 ]
机构
[1] Johns Hopkins Univ, Sch Med, 733 North Broadway, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Dept Pathol, Sch Med, 1800 Orleans St, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ, Russell H Morgan Dept Radiol & Radiol Sci, Musculoskeletal Radiol, Sch Med, 600 North Wolfe St, Baltimore, MD 21287 USA
[4] Johns Hopkins Univ Hosp, Div Orthopaed Oncol, Dept Orthopaed Surg, 601 North Caroline St, Baltimore, MD 21287 USA
关键词
Adult rhabdomyosarcoma; Pleomorphic rhabdomyosarcoma; Primary rhabdomyosarcoma of bone; ALVEOLAR RHABDOMYOSARCOMA; LONG-BONE; DEDIFFERENTIATED CHONDROSARCOMA; PLEOMORPHIC RHABDOMYOSARCOMA; CHILDHOOD-CANCER;
D O I
10.1007/s00256-016-2430-7
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Primary rhabdomyosarcoma of the bone is an extremely rare condition with few examples reported in the literature. We present the case of a 34-year-old male who presented with a lesion in the distal femur with initial imaging features consistent with Ewing sarcoma. Histologically, the lesion consisted of atypical pleomorphic polygonal rhabdomyoblasts demonstrating focal desmin and myogenin expression. A diagnosis of pleomorphic rhabdomyosarcoma was rendered. Despite systemic treatment and surgery, this patient experienced a rapidly progressive disease course. We believe this is only the second report in the orthopedic literature of a case of primary pleomorphic rhabdomyosarcoma of the bone. The key imaging, pathologic, and clinical findings are discussed.
引用
收藏
页码:1391 / 1395
页数:5
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