Hamada T, Ito H, Araki Y, Fujii K, Inoue M, Ishida O
Department of Radiology, Kinki University School of Medicine, Osaka, Japan.
Skeletal Radiol. 1996 Jan;25(1):25-9. doi: 10.1007/s002560050027.
Benign fibrous histiocytoma is a tumor with histologic features similar to those of xanthofibromas, which include fibrous cortical defects and nonossifying fibromas, but with different clinical features. This study investigated the findings of benign fibrous histiocytoma on various imaging modalities. It emphasized the importance of clinical and imaging features as well as histologic findings in establishing the diagnosis.
We reviewed three cases of benign fibrous histiocytoma of the femur that had been diagnosed histologically as (fibro)xanthoma during a retrospective analysis of 187 primary benign and malignant bone lesions.
All the patients were middle-aged women with various knee complaints.
Radiologically, the lesions were all lytic with well-defined geographic margins and sclerotic rims. The tumors arose within the medullary cavity in the distal metaphysis of the femur and involved the epiphysis. CT showed lytic destruction with well-defined marginal sclerosis. T1-weighted MR images showed that the lesions had predominantly the same signal intensity as that of skeletal muscle. The lesions were hypovascular on angiography. Bone scintigraphy showed moderately increased uptake. It was concluded that multiple images as well as clinical features can be useful in differentiating benign fibrous histiocytoma from fibroxanthoma, giant cell tumor, and other fibrohistiocytic tumors of bone.
良性纤维组织细胞瘤是一种组织学特征与黄色纤维瘤相似的肿瘤,黄色纤维瘤包括纤维皮质缺损和非骨化性纤维瘤,但具有不同的临床特征。本研究调查了良性纤维组织细胞瘤在各种影像学检查中的表现。强调了临床和影像学特征以及组织学检查结果在确立诊断中的重要性。
在对187例原发性良恶性骨病变的回顾性分析中,我们复查了3例经组织学诊断为(纤维)黄色瘤的股骨良性纤维组织细胞瘤病例。
所有患者均为中年女性,有各种膝关节症状。
放射学上,病变均为溶骨性,边界清晰呈地图样,有硬化边缘。肿瘤起源于股骨远端干骺端的髓腔内,并累及骨骺。CT显示溶骨性破坏,边缘硬化清晰。T1加权磁共振成像显示病变的信号强度与骨骼肌基本相同。血管造影显示病变血管较少。骨闪烁显像显示摄取中度增加。得出结论,多种影像学检查以及临床特征有助于将良性纤维组织细胞瘤与纤维黄色瘤、骨巨细胞瘤及其他骨纤维组织细胞性肿瘤相鉴别。