Verma Shyam B, Desai Hitesh K, Shah Vishal N, Happle Rudolf
Nirvana Skin Clinic, Vadodara, Gujarat, India.
KG Patel Children Hospital, Vadodara, Gujarat, India.
Indian J Dermatol. 2017 Mar-Apr;62(2):207-209. doi: 10.4103/0019-5154.201760.
A 2-month-old boy was presented with widespread lateralized blue macules (nevus cesius), an extensive nevus flammeus, and large patches of cutis marmorata telangiectatica congenita. Moreover, he had macrocephaly, a coarse facial appearance with depressed nasal bridge, retinal abnormalities, septal defects of the heart, and obliteration of the left brachiocephalic vein and major veins of the left arm with pronounced collateralization. The multisystem disorder of this boy cannot be categorized within the present classification of distinct types of phacomatosis pigmentovascularis. Although some similar complex cases have previously been reported, it seems too early to give them a specific name. Rather, the present case should be included, so far, into the group of unclassifiable types of phacomatosis pigmentovascularis.
一名2个月大的男婴表现为广泛的单侧蓝色斑(青色痣)、大片鲜红斑痣以及大片先天性网状青斑。此外,他还患有巨头畸形、面部粗糙、鼻梁凹陷、视网膜异常、心脏间隔缺损,以及左头臂静脉和左臂主要静脉闭塞并伴有明显的侧支循环形成。该男婴的多系统疾病无法归入目前色素血管性错构瘤病的不同类型分类中。尽管此前曾报道过一些类似的复杂病例,但现在为它们赋予特定名称似乎还为时过早。相反,目前该病例应暂时归入色素血管性错构瘤病不可分类类型组。