无面部痣的伊藤色素减退症与斯特奇-韦伯综合征：一种关联还是一种新综合征？

Hypomelanosis of Ito and Sturge-Weber syndrome without facial nevus: an association or a new syndrome?

作者信息

Değerliyurt Aydan, Kantar Asli, Ceylaner Serdar, Aysun Sabiha

机构信息

Department of Pediatric Neurology, Ankara Diskapi Children's Hospital, Ankara, Turkey.

出版信息

Pediatr Neurol. 2009 May;40(5):395-7. doi: 10.1016/j.pediatrneurol.2008.11.017.

DOI:10.1016/j.pediatrneurol.2008.11.017

PMID:19380080

Abstract

Sturge-Weber syndrome without facial nevus is rare. Twenty-four cases were previously reported. Although hypomelanosis of Ito is a relatively common disorder, there was only one previous case in association with Sturge-Weber syndrome. We describe an 11-year-old boy with Sturge-Weber syndrome without facial nevus, coexistent with hypomelanosis of Ito.

摘要

无面部痣的斯特奇-韦伯综合征很罕见。此前曾报道过24例。虽然伊藤色素减退症是一种相对常见的疾病，但此前仅有1例与斯特奇-韦伯综合征相关。我们描述了一名11岁无面部痣的斯特奇-韦伯综合征男孩，同时合并伊藤色素减退症。