软组织的软骨瘤

Applied pathology Pub Date : 1988-01-01
C D Fletcher, T Krausz
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引用次数: 0

摘要

软组织肿瘤可表现为软骨分化为原发性现象(如软骨瘤或骨外黏液样和间充质软骨肉瘤)或继发性化生特征(最明显的是骨外骨肉瘤或恶性神经鞘肿瘤)。本文回顾了原发性软骨肿瘤的文献,并对其鉴别诊断进行了讨论。软组织软骨瘤值得注意的是其倾向于表现出明显的核多形性。骨外软骨肉瘤比骨外软骨肉瘤罕见得多,仅占软组织肉瘤的1-2%。几乎所有的肉瘤都可分为黏液样或间质亚型,其中黏液样预后较好。可能表现局灶性软骨化生的软组织肿瘤的讨论更为简单。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cartilaginous tumours of soft tissue.

Tumours of soft tissue may manifest cartilaginous differentiation as a primary phenomenon (as in chondromas or extraskeletal myxoid and mesenchymal chondrosarcomas) or as a secondary metaplastic feature (most notably in extraskeletal osteosarcomas or malignant nerve sheath tumours). The literature regarding primary cartilaginous tumours is reviewed and their differential diagnosis discussed. Soft tissue chondromas are noteworthy for their tendency to show significant nuclear pleomorphism. Extraskeletal chondrosarcoma is much rarer than its osseous counterpart, accounting for only 1-2% of soft tissue sarcomas. Virtually all such sarcomas can be classified into the myxoid or mesenchymal subtypes, of which myxoid carries a better prognosis. Soft tissue neoplasms which may show focal cartilaginous metaplasia are covered more briefly.

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