Suppr超能文献

面部血管瘤伴脑血管异常和小脑发育不全。

Facial hemangioma with cerebrovascular anomalies and cerebellar hypoplasia.

作者信息

Mizuno Y, Kurokawa T, Numaguchi Y, Goya N

出版信息

Brain Dev. 1982;4(5):375-8. doi: 10.1016/s0387-7604(82)80022-3.

Abstract

A 5-year-old female patient with a left facial strawberry nevus, ipsilateral optic atrophy and cerebellar signs was observed. Computed tomography and cerebral angiography confirmed left cerebellar hypoplasia and cerebrovascular abnormalities such as internal carotid arterial stenosis, basilar artery occlusion, and a saccular aneurysm of left carotid siphon, all of which are presumed to develop congenitally. This case may represent a new variety of neurocutaneous syndrome which is different from other syndromes associated with facial hemangioma, such as the Sturge-Weber syndrome and the Wyburn-Mason syndrome.

摘要

观察到一名5岁女性患者,有左侧面部草莓状痣、同侧视神经萎缩和小脑体征。计算机断层扫描和脑血管造影证实左侧小脑发育不全以及脑血管异常,如颈内动脉狭窄、基底动脉闭塞和左侧颈内动脉虹吸部囊状动脉瘤,所有这些都被认为是先天性发育而来。该病例可能代表一种新型的神经皮肤综合征,与其他与面部血管瘤相关的综合征,如斯特奇-韦伯综合征和怀伯恩-梅森综合征不同。

相似文献

1
Facial hemangioma with cerebrovascular anomalies and cerebellar hypoplasia.
Brain Dev. 1982;4(5):375-8. doi: 10.1016/s0387-7604(82)80022-3.
6
Hereditary neurocutaneous angiomatosis. Report of four cases.
J Neurosurg. 1996 Dec;85(6):1135-42. doi: 10.3171/jns.1996.85.6.1135.
7
A new 3C syndrome: cerebellar hypoplasia, cavernous haemangioma and coarctation of the aorta.
Dev Med Child Neurol. 1993 Jul;35(7):637-41. doi: 10.1111/j.1469-8749.1993.tb11702.x.
8
Extensive facial strawberry mark associated with cerebellar hypoplasia and vascular abnormalities.
J Dermatol. 1997 Feb;24(2):113-6. doi: 10.1111/j.1346-8138.1997.tb02754.x.
10
[A case of Wyburn-Mason syndrome].
Rinsho Shinkeigaku. 1989 Aug;29(8):1039-44.

引用本文的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验