Phakomatosis Pigmentovascularis Type IIb Associated with Sturge‐Weber Syndrome
Phakomatosis Pigmentovascularis Type IIb Associated with Sturge‐Weber Syndrome
复制标题
与 Sturge-Weber 综合征相关的 IIb 型血管色素瘤病
作者：
Ahmad A. Al Robaee;N. Banka;A. Alfadley
翻译后摘要：我们描述了一个23个月大的儿童与色素性血管瘤病IIb型与斯特奇-韦伯综合征。 色素血管性斑痣病是一种罕见的皮肤畸形，其特征是同时发生鲜红斑痣和黑素细胞痣。本文简要回顾了文献，并讨论了这种罕见疾病的分类。
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.