与斯-韦综合征相关的IIb型色素血管性斑痣性错构瘤病
Phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome.
作者信息
Al Robaee Ahmad, Banka Nusrat, Alfadley Abdullah
机构信息
Department of Medicine, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia.
出版信息
Pediatr Dermatol. 2004 Nov-Dec;21(6):642-5. doi: 10.1111/j.0736-8046.2004.21605.x.
Abstract
We describe a 23-month-old child with phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome. Phakomatosis pigmentovascularis type IIb is a rare cutaneous malformation characterized by the simultaneous occurrence of nevus flammeus and melanocytic nevi. A brief review of the literature is presented and classification of this rare disease is discussed.
摘要
我们描述了一名患有与斯特奇-韦伯综合征相关的IIb型色素血管性斑痣性错构瘤病的23个月大儿童。IIb型色素血管性斑痣性错构瘤病是一种罕见的皮肤畸形，其特征为火焰状痣和黑素细胞痣同时出现。本文对相关文献进行了简要综述，并讨论了这种罕见疾病的分类。
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