Visset J, Mussini-Montpellier J, Paineau J
J Chir (Paris). 1979 Nov;116(11):641-4.
It is classical to consider desmoid tumours as an entity with only a local prognosis, conditioned by the frequency of relapses. In this respect, they are different from other mesenchymatous tumours, fibrosarcomas in particular which have a poorer prognosis. The authors report the case of a 23 years old man with a tumour of the abdominal wall, which in the early stages resembled a desmoid tumour, but the development of metastases suggested a sarcoma. This observation seems to make doubtful the distinction between desmoid tumour and fibrosarcoma, and thus the prognosis of tumours with a desmoid appearance. Under these conditions, this term should only be used for descriptive purposes and has no prognostic value.
传统上认为硬纤维瘤是一种仅具有局部预后的实体瘤，其预后受复发频率的影响。在这方面，它们与其他间叶组织肿瘤不同，尤其是纤维肉瘤，后者预后较差。作者报告了一名23岁男性腹壁肿瘤的病例，该肿瘤早期类似硬纤维瘤，但转移灶的出现提示为肉瘤。这一观察结果似乎使硬纤维瘤和纤维肉瘤之间的区别以及硬纤维瘤样外观肿瘤的预后变得可疑。在这种情况下，该术语仅应用于描述目的，不具有预后价值。
