Primary perivascular epithelioid cell neoplasm (PEComa) of bone: Report of two cases and review of the literature

被引:10
|
作者
Desy, Nicholas M. [1 ]
Bernstein, Mitchell [1 ]
Nahal, Ayoub [2 ]
Aziz, Mohamed [3 ]
Kenan, Samuel [4 ]
Turcotte, Robert E. [1 ]
Kahn, Leonard B. [3 ]
机构
[1] McGill Univ, Ctr Hlth, Dept Orthopaed Surg, Montreal, PQ H3G 1A4, Canada
[2] McGill Univ, Ctr Hlth, Dept Pathol, Montreal, PQ H3G 1A4, Canada
[3] N Shore LIJ Hlth Syst, Dept Pathol, New York, NY USA
[4] N Shore LIJ Hlth Syst, Dept Orthopaed Surg, New York, NY USA
关键词
Perivascular epithelioid cell neoplasm; PEComa; Bone; Acetabulum; Fibula; TUMOR PECOMA; ANGIOMYOLIPOMA; MEMBER; FAMILY; SUGAR; TFE3;
D O I
10.1007/s00256-012-1479-1
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 perivascular epithelioid cell neoplasms (PEComas) of bone are rare mesenchymal tumors. Histologically, they are composed predominantly of perivascular epithelioid cells and have the capacity to metastasize. PEComas have been reported within intra-abdominal and intra-pelvic organs. To the best of our knowledge, only seven primary PEComas of bone have been described in the English literature. We present two cases of PEComa of bone, one arising from the distal fibula and one from the acetabulum. Both were treated by surgical excision and one also received adjuvant chemotherapy.
引用
收藏
页码:1469 / 1474
页数:6
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