Jung W H, Choi S, Oh K K, Chi J G
Department of Pathology and Radiology, Yong Dong Severance Hospital, Yonsei University, College of Medicine, Seoul, Korea.
J Korean Med Sci. 1990 Dec;5(4):225-31. doi: 10.3346/jkms.1990.5.4.225.
A congenital neoplasm arising in the central nervous system is rarely encountered, and the majority of case reports that have dealt with intracranial tumors have been divided almost equally between teratomas and various gliomas. We experienced a rare case of congenital glioblastoma multiforme encountered in a three day-old male infant who presented with hydrocephalus since birth. Post-mortem examination revealed that the tumor seemed to have originated from the right thalamic region extending centrifugally to the cerebral cortex and through the brain-stem down to the cerebellum.
中枢神经系统先天性肿瘤极为罕见,大多数有关颅内肿瘤的病例报告中,畸胎瘤和各种胶质瘤的比例几乎相等。我们遇到了一例罕见的先天性多形性胶质母细胞瘤病例,患儿为一名3日龄男婴,自出生起就患有脑积水。尸检显示,肿瘤似乎起源于右丘脑区域,呈离心性扩展至大脑皮层,并通过脑干延伸至小脑。