O'Connell J X, Trotter M J
Department of Pathology and Laboratory Medicine, Vancouver Hospital, British Columbia, Canada.
Mod Pathol. 1996 Mar;9(3):273-8.
We report two examples of dermatofibrosarcoma protuberans with fibrosarcomatous change, in which the fibrosarcomatous component of the tumor demonstrated focal myofibroblastic differentiation. This was recognized by light microscopy as plump myoid cells associated with abundant extracellular collagen production, immunohistochemically by positive staining for smooth muscle and muscle specific actin, and ultrastructurally by subplasmalemmal filament aggregates and micropinocytotic vesicles. Myofibroblastic differentiation has not been described before in dermatofibrosarcoma protuberans with fibrosarcomatous change and because of a lack of information concerning the immunohistochemical profile of this variant of DFSP its incidence is unknown. Focal myofibroblastic differentiation, as demonstrated in the fibrosarcomatous regions of these two tumors, might support the proposed dermal fibroblastic origin for dermatofibrosarcoma protuberans with fibrosarcomatous change.
我们报告了两例伴有纤维肉瘤样改变的隆突性皮肤纤维肉瘤,其中肿瘤的纤维肉瘤成分显示出局灶性肌成纤维细胞分化。光镜下表现为丰满的肌样细胞并伴有大量细胞外胶原产生,免疫组化显示平滑肌和肌肉特异性肌动蛋白呈阳性染色,超微结构可见质膜下细丝聚集和微吞饮小泡,从而得以识别。伴有纤维肉瘤样改变的隆突性皮肤纤维肉瘤此前尚未见有肌成纤维细胞分化的报道,由于缺乏关于该DFSP变体免疫组化特征的信息,其发生率尚不清楚。这两例肿瘤纤维肉瘤区域所显示的局灶性肌成纤维细胞分化,可能支持了伴有纤维肉瘤样改变的隆突性皮肤纤维肉瘤起源于真皮成纤维细胞的观点。