Rao A S, Vigorita V J
J Bone Joint Surg Am. 1984 Jan;66(1):76-94.
We reviewed the cases of eighty-one patients with pigmented villonodular synovitis and giant-cell tumor of the tendon sheath. The average duration of symptoms prior to consulting a physician was twenty-seven months. The lesion was slow-growing, was located in one joint or tendon sheath, and usually was asymptomatic in a finger or thumb but painful in a knee or toe. Twenty-nine per cent of the finger or thumb lesions and 21 per cent of the knee lesions that were followed recurred. Approximately 70 per cent of the radiographs showed abnormalities that ranged from soft-tissue swelling to bone erosion. Six lesions were incidental findings during arthrotomy for some other lesion. The histological characteristics of the solitary nodular, multiple nodular, and diffuse lesions suggested that they have a common histogenesis that is characterized by proliferation of fibroblastic or histiocytic mesenchymal cells, or both, beneath the synovial or tenosynovial lining cells, and by collagen production. Foam cells and iron deposits appear to be secondary changes and are usually seen in the periphery of the expanding nodules. The centrifugal growth pattern and the distinct differences between the lesional tissue and the adjacent hyperplastic synovial tissue suggest that pigmented villonodular synovitis is a true neoplastic process.
我们回顾了81例色素沉着绒毛结节性滑膜炎和腱鞘巨细胞瘤患者的病例。就诊前症状的平均持续时间为27个月。病变生长缓慢,位于一个关节或腱鞘,通常在手指或拇指无症状,但在膝关节或脚趾疼痛。随访的手指或拇指病变中有29%复发,膝关节病变中有21%复发。约70%的X线片显示异常,范围从软组织肿胀到骨质侵蚀。6个病变是在因其他病变进行关节切开术时偶然发现的。孤立结节性、多发结节性和弥漫性病变的组织学特征表明它们有共同的组织发生,其特征是滑膜或腱鞘内衬细胞下方的成纤维细胞或组织细胞间充质细胞或两者增殖,并产生胶原蛋白。泡沫细胞和铁沉积似乎是继发性改变,通常见于扩大结节周边。离心生长模式以及病变组织与相邻增生滑膜组织之间的明显差异表明色素沉着绒毛结节性滑膜炎是一个真正的肿瘤性过程。