Kutzner H, Hügel H, Rütten A, Braun M
Dermatologische Gemeinschaftspraxis, Friedrichshafen.
Hautarzt. 1993 Sep;44(9):561-8.
Adult myofibroma is an acquired skin tumour that is histologically identical to infantile myofibroma. Histologically, four tumour variants can be distinguished: leiomyoma type, cellular spindle cell type, haemangiopericytoma or glomus type, and biphasic type. Practical help in diagnosis is supplied by the hamartomatous composition of the leiomyoma-type, hyalinized spindle cell whorls, endothelium-lined haemangiopericytoma-like vascular channels, and desmin-negative, muscle-actin-positive myofibroblasts, which may show spindle cell or undifferentiated mesenchymal cell differentiation. The tumours clinically present as firm, occasionally bluish cutaneous or subcutaneous nodules. Adult myofibroma should be recognized as a distinct benign neoplasm, most probably of vascular origin. Clinicians and dermatopathologists must be aware that lesions identical to those of infantile myofibroma can occur in adults.
成人肌纤维瘤是一种后天性皮肤肿瘤,在组织学上与婴儿肌纤维瘤相同。在组织学上,可区分出四种肿瘤变体:平滑肌瘤型、细胞性梭形细胞型、血管外皮细胞瘤或血管球型以及双相型。平滑肌瘤型的错构瘤成分、玻璃样变性的梭形细胞漩涡、内皮衬里的血管外皮细胞瘤样血管通道以及结蛋白阴性、肌动蛋白阳性的肌成纤维细胞(可能显示梭形细胞或未分化间充质细胞分化)为诊断提供了实际帮助。这些肿瘤临床上表现为坚实的、偶尔呈蓝色的皮肤或皮下结节。成人肌纤维瘤应被视为一种独特的良性肿瘤,很可能起源于血管。临床医生和皮肤病理学家必须意识到,与婴儿肌纤维瘤相同的病变也可发生于成人。