Seguin P, Pascal J F, Dumollard J M, Momège B, Achard R
Service de Stomatologie et de Chirurgie Maxillo-faciale, Hôpital de Bellevue, Saint-Etienne.
Rev Stomatol Chir Maxillofac. 1989;90(5):305-12.
Malignant fibrous histiocytomas, or MFH, have been individualized only since the last two decades. These sarcomas which usually develop from soft tissues are no longer considered rare, except in some of their facial sinus localizations. Two chapters will be particularly developed: the paramount significance of anatomopathological investigations owing to the difficulty in establishing the diagnosis, since MFHs may be mistaken for benign processes; the treatment which is, generally speaking, the same as for bone sarcomas.
恶性纤维组织细胞瘤（MFH）直到过去二十年才被单独分类。这些通常起源于软组织的肉瘤已不再被视为罕见疾病，不过在某些面部鼻窦部位的情况除外。本文将特别展开两个章节：鉴于MFH可能被误诊为良性病变，病理检查对于诊断确立存在困难，因此其具有至关重要的意义；一般而言，其治疗方法与骨肉瘤相同。
