一名患有太田痣、广泛蒙古斑、鲜红斑痣、贫血痣和先天性毛细血管扩张性大理石样皮肤的男孩病例：色素血管性斑痣性错构瘤病的一个独特实例。
The case of a boy with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita: a unique instance of phacomatosis pigmentovascularis.
作者信息
Ma Han, Liao Mengsi, Qiu Shu, Luo Ruijun, Lu Rongbiao, Lu Chun
机构信息
Third Affi liated Hospital, Sun Yat-sen Universit, Guangdong, CN.
出版信息
An Bras Dermatol. 2015 May-Jun;90(3 Suppl 1):10-2. doi: 10.1590/abd1806-4841.20153466.
Abstract
Phacomatosis pigmentovascularis is a rare, congenital condition characterized by a combination of cutaneous melanocytic lesions and vascular malformation. We discuss an entirely unique case of Phacomatosis pigmentovascularis with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita, which may represent a heretofore undescribed variant of phacomatosis pigmentovascularis.
摘要
色素血管性斑痣性错构瘤病是一种罕见的先天性疾病，其特征为皮肤黑素细胞病变和血管畸形并存。我们讨论了一例极为独特的色素血管性斑痣性错构瘤病病例，该病例伴有太田痣、广泛的蒙古斑、鲜红斑痣、贫血痣和先天性毛细血管扩张性大理石样皮肤，这可能代表了一种迄今尚未描述的色素血管性斑痣性错构瘤病变体。
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