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皮质软骨母细胞瘤:1例报告及该病变在不寻常部位报道的文献综述

Cortical chondroblastoma: report of a case and literature review of this lesion reported in unusual locations.

作者信息

Hameed Meera R, Blacksin Marcia, Das Kasturi, Patterson Francis, Benevenia Joseph, Aisner Seena

机构信息

New Jersey Medical School of Pathology, University of Medicine and Dentistry, Newark, NJ, USA.

出版信息

Skeletal Radiol. 2006 May;35(5):295-7. doi: 10.1007/s00256-005-0035-7. Epub 2006 Feb 25.

DOI:10.1007/s00256-005-0035-7
PMID:16501973
Abstract

Chondroblastoma is a rare benign tumor occurring in adolescence and young adulthood, almost always involving the epiphysis of long bones. A 24-year-old man presented with a discrete soft-tissue lesion penetrating the cortex of the right distal femoral metadiaphyseal region. Biopsy revealed a chondroblastoma, and the patient subsequently underwent a total curettage of the lesion with cancellous bone graft from the iliac crest.

摘要

软骨母细胞瘤是一种罕见的良性肿瘤,发生于青少年和青年时期,几乎总是累及长骨的骨骺。一名24岁男性患者出现一个孤立的软组织病变,穿透右股骨远端干骺端区域的皮质。活检显示为软骨母细胞瘤,患者随后接受了病变的彻底刮除术,并取自体髂骨松质骨移植。

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Cortical chondroblastoma: report of a case and literature review of this lesion reported in unusual locations.皮质软骨母细胞瘤:1例报告及该病变在不寻常部位报道的文献综述
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