Kokshunova L E
Arkh Patol. 1980;42(1):63-5.
An observation of a rare congenital multiple tumor of the heart with histological structure of rhabdomyoma is described. Of interest is the presence in the child with congenital rhabdomyoma of the heart of dysplastic changes in the kidneys in the form of few small cysts and in the brain in the form of angiomatous structures. Such combination confirms dysontogenetic origin of rhabdomyoma.
本文描述了一例具有横纹肌瘤组织学结构的罕见先天性心脏多发性肿瘤的观察情况。值得关注的是,患有先天性心脏横纹肌瘤的儿童同时存在肾脏发育异常改变,表现为少量小囊肿,以及脑部存在血管瘤样结构。这种组合证实了横纹肌瘤的发育异常起源。