Demiralp Bahtiyar, Ozdemir M Taner, Erler Kaan, Basbozkurt Mustafa
Gulhane Military Medical Academy, Department of Orthopaedics, Ankara, Turkey.
Acta Orthop Belg. 2007 Jun;73(3):403-7.
We report two cases of malignant soft-tissue tumours--one myxoid malignant fibrous histiocytoma and one pleomorphic rhabdomyosarcoma--which were diagnosed in two young adult patients with type 1 neurofibromatosis (NF 1). The patients were evaluated with criteria for Neurofibromatosis 1 and NF 1 gene analysis was performed. Four of seven criteria were found in both patients. The tumours were stage II and III respectively. Both patients were treated with radiotherapy or chemotherapy and surgical intervention. Diagnoses of myxoid malignant fibrous histiocytoma and pleomorphic rhabdomyosarcoma in adult NF 1 patients are exceedingly rare. Thus detection of subtypes of rhabdomyosarcoma and malignant fibrous histiocytoma with immunohistochemistry may be helpful for the management of these tumours among other pleomorphic sarcomas that may occur in type 1 Neurofibromatosis.
我们报告了两例恶性软组织肿瘤——一例黏液样恶性纤维组织细胞瘤和一例多形性横纹肌肉瘤——这两例肿瘤分别在两名患有1型神经纤维瘤病(NF 1)的年轻成年患者中被诊断出来。对这两名患者进行了1型神经纤维瘤病的标准评估,并进行了NF 1基因分析。两名患者均符合七项标准中的四项。肿瘤分别处于II期和III期。两名患者均接受了放疗或化疗以及手术干预。成年NF 1患者中黏液样恶性纤维组织细胞瘤和多形性横纹肌肉瘤的诊断极为罕见。因此,通过免疫组织化学检测横纹肌肉瘤和恶性纤维组织细胞瘤的亚型,可能有助于在1型神经纤维瘤病中可能出现的其他多形性肉瘤中对这些肿瘤进行管理。