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富含破骨细胞的骨肉瘤

Osteoclast-rich osteosarcoma.

作者信息

Bathurst N, Sanerkin N, Watt I

出版信息

Br J Radiol. 1986 Jul;59(703):667-73. doi: 10.1259/0007-1285-59-703-667.

Abstract

Nine cases of primary osteoclast-rich osteosarcoma, an undifferentiated sarcoma with an overabundance of osteoclasts and a paucity of tumour osteoid, are reported. They comprise about 3% of all primary osteosarcomas and are histologically related to telangiectatic osteosarcoma, another undifferentiated tumour with abundant osteoclasts and scanty osteoid, perhaps being a predominantly solid variant of the latter. Many of the classical radiological features of an osteosarcoma are absent in these cases and differentiation from a benign lesion is sometimes difficult. Typically, an ill-defined margin surrounds a predominantly lytic lesion of the diaphysis or metaphysis of the femur or tibia of a young patient. A soft-tissue mass is not usually present and periosteal reaction is scanty.

摘要

本文报告了9例原发性富含破骨细胞的骨肉瘤,这是一种未分化肉瘤,其破骨细胞数量过多而肿瘤类骨质较少。它们约占所有原发性骨肉瘤的3%,在组织学上与毛细血管扩张性骨肉瘤相关,后者是另一种未分化肿瘤,有丰富的破骨细胞和少量类骨质,可能是前者的主要实体变体。这些病例缺乏许多骨肉瘤的典型放射学特征,有时难以与良性病变区分开来。通常,边界不清的病变围绕着年轻患者股骨或胫骨骨干或干骺端的主要溶骨性病变。通常不存在软组织肿块,骨膜反应较少。

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