Ito H, Kishikawa T, Toda T, Arai M, Muro H
J Pediatr Surg. 1984 Jun;19(3):315-7. doi: 10.1016/s0022-3468(84)80197-9.
An 8-month-old boy was found to have a solitary hepatic mesenchymal hamartoma. Histologically, the lesion appeared as a large island of loose mesenchymal tissue with few cystic bile ducts and liver cells. Electronmicroscopy showed microvilli on the surface of tumor cells and desmosomes between the cells. Immunohistochemical studies showed that alpha-fetoprotein was localized in the proliferating liver cells and bile ductal epithelium of this neoplasm. This case is the 17th case of hepatic mesenchymal hamartoma reported in Japan.
一名8个月大的男婴被发现患有孤立性肝间叶性错构瘤。组织学上,病变表现为一大片疏松的间叶组织岛,伴有少量囊性胆管和肝细胞。电子显微镜检查显示肿瘤细胞表面有微绒毛,细胞间有桥粒。免疫组织化学研究表明,甲胎蛋白定位于该肿瘤增殖的肝细胞和胆管上皮中。该病例是日本报道的第17例肝间叶性错构瘤。