Ishida T, Machinami R, Kojima T, Kikuchi F
Department of Pathology, Faculty of Medicine, University of Tokyo, Japan.
Pathol Res Pract. 1992 Aug;188(6):757-63. doi: 10.1016/S0344-0338(11)80174-3.
Three cases of bone sarcomas arising in fibrous dysplasia (FD) without prior radiation therapy were reported. One of the tumors was a conventional osteoblastic osteosarcoma (OS) and the other two were malignant fibrous histiocytomas (MFH). The lesion of FD was monostotic in two patients and polyostocic (monomelic) in one. Bone sarcomas and FD were detected simultaneously in all cases. One of the MFH cases died 6 months after diagnosis, and the other MFH case and the OS case are alive without disease 3 years and one and a half years after surgery, respectively. Conservative treatment has been selected in most of the patients of FD. We should closely follow up these patients, because bone sarcomas such as OS and MFH could arise at the site of FD. This is the first report of the cases of MFH of bone arising in FD.
报告了3例未接受过放疗的纤维发育不良(FD)相关骨肉瘤病例。其中1例肿瘤为传统成骨细胞性骨肉瘤(OS),另外2例为恶性纤维组织细胞瘤(MFH)。2例患者的FD病变为单骨型,1例为多骨型(单肢型)。所有病例中骨肉瘤和FD均同时被发现。1例MFH患者在诊断后6个月死亡,另1例MFH患者和OS患者分别在手术后3年和1年半无病存活。大多数FD患者选择了保守治疗。我们应密切随访这些患者,因为FD部位可能发生OS和MFH等骨肉瘤。这是首例关于FD相关骨MFH病例的报告。