| Literature DB >> 1700324 |
H Nakagawa1, Y Furuta, S Nakajima, A Murasawa, Y Nakajima.
Abstract
The authors report on a surgical case of cavernous angioma in the pontomedullary region. A 60-year-old male exhibited a progressive neurological deficit consisting mainly of bulbar paresis and cerebellar signs, without ictal episodes, and computed tomographic scans showed growth of the lesion over 3 years. On preoperative assessment, a glial tumor was suspected to coexist with a cavernous angioma. The vascular malformation was totally excised successfully. This case also revealed an unusual familial occurrence.Entities:
Mesh:
Year: 1990 PMID: 1700324 DOI: 10.2176/nmc.30.422
Source DB: PubMed Journal: Neurol Med Chir (Tokyo) ISSN: 0470-8105 Impact factor: 1.742