Larralde Margarita, Santos-Muñoz Andrea, Rodríguez Cáceres María, Ciardiullo Analía
Department of Pediatric Dermatology, Ramos Mejía Hospital, Buenos Aires, Argentina.
Pediatr Dermatol. 2008 Mar-Apr;25(2):198-200. doi: 10.1111/j.1525-1470.2008.00633.x.
Phacomatosis pigmentovascularis is a rare genodermatosis characterized by a combination of melanocytic nevi and vascular malformations. A new type of phacomatosis pigmentovascularis was recently described which included cutis marmorata telangiectatica congenita and aberrant Mongolian spots and was named type V. We report a 3-month-old girl with diagnosis of phacomatosis pigmentovascularis type V.
色素血管性斑痣性错构瘤病是一种罕见的遗传性皮肤病，其特征为黑素细胞痣和血管畸形并存。最近描述了一种新型的色素血管性斑痣性错构瘤病，其中包括先天性毛细血管扩张性大理石样皮肤和异常蒙古斑，被命名为V型。我们报告了一名3个月大的女孩，诊断为V型色素血管性斑痣性错构瘤病。
