Fletcher C D, Krausz T
Department of Histopathology, St. Thomas's Hospital Medical School, London, UK.
Appl Pathol. 1988;6(3):208-20.
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.
软组织肿瘤可能会将软骨分化作为一种原发性现象(如软骨瘤或骨外黏液样和间叶性软骨肉瘤),或作为一种继发性化生特征(最显著的是在骨外骨肉瘤或恶性神经鞘瘤中)。本文回顾了有关原发性软骨肿瘤的文献,并讨论了它们的鉴别诊断。软组织软骨瘤因其显示出明显核多形性的倾向而值得注意。骨外软骨肉瘤比其骨内对应物罕见得多,仅占软组织肉瘤的1%-2%。几乎所有这类肉瘤都可分为黏液样或间叶性亚型,其中黏液样亚型预后较好。可能表现为局灶性软骨化生的软组织肿瘤则进行更简要的阐述。