Palungwachira P, Shirai M, Iwahara K, Ogawa H
Srinakharinwirot Skin Center, Srinakharinwirot University, Bangkok, Thailand.
J Med Assoc Thai. 1998 May;81(5):371-8.
Clinical, histopathologic and electronmicroscopic findings in a case of congenital localized multiple fibromatosis of interscapular region are presented. This 10 year-old Japanese girl developed this lesion since she was 3 weeks old, metastases have never been observed. The histological and electron-microscopic features point to the hamartomous origin of this tumor with partial differentiation of its cells towards myofibroblasts and atypical fibroblasts. The differential diagnosis from other soft tissue tumors in infancy and early childhood is discussed.
本文报告了一例先天性肩胛间区局限性多发性纤维瘤病的临床、组织病理学和电子显微镜检查结果。这名10岁的日本女孩自3周大时就出现了这种病变，从未观察到转移情况。组织学和电子显微镜特征表明该肿瘤起源于错构瘤，其细胞部分分化为肌成纤维细胞和非典型成纤维细胞。文中还讨论了与婴幼儿期其他软组织肿瘤的鉴别诊断。
