伴有相关巨大动脉瘤的促结缔组织增生性婴儿型节细胞胶质瘤——病例报告

Desmoplastic infantile ganglioglioma with associated giant aneurysm—case report.

作者信息

To Chiu Yuen, Rajah Gary, Klein Elizabeth, McNaughton Michelle, Ham Steven, Haridas Abilash, Kupsky William, Marin Horia, Sood Sandeep

机构信息

Department of Neurosurgery, Detroit Medical Center, Wayne State University, Detroit, MI, USA,

出版信息

Childs Nerv Syst. 2015 Aug;31(8):1413-8. doi: 10.1007/s00381-015-2722-6. Epub 2015 Apr 29.

DOI:10.1007/s00381-015-2722-6

PMID:25922053

Abstract

Desmoplastic infantile ganglioglioma (DIG) and supratentorial giant cerebral aneurysm are each extremely rare entities in infants. Here, we present the case of an 8-day old boy who had both of these conditions concurrently. To our knowledge, there is no previous case reported of a patient with coexisting DIG and giant aneurysm.

摘要

促结缔组织增生性婴儿型节细胞胶质瘤（DIG）和幕上巨大脑动脉瘤在婴儿中均极为罕见。在此，我们报告一例同时患有这两种疾病的8日龄男婴病例。据我们所知，此前尚无DIG与巨大动脉瘤并存患者的病例报道。