两篇关于IIb型色素血管性斑痣性错构瘤病的报告，其中一篇与斯-韦综合征和克-特综合征相关。
Two reports of phacomatosis pigmentovascularis type IIb, one in association with Sturge-Weber syndrome and Klippel-Trenaunay syndrome.
作者信息
Finklea Lindsey B, Mohr Melinda R, Warthan Molly M, Darrow David H, Williams Judith V
机构信息
Department of Dermatology, Eastern Virginia Medical School, Norfolk, Virginia 23507, USA.
出版信息
Pediatr Dermatol. 2010 May-Jun;27(3):303-5. doi: 10.1111/j.1525-1470.2010.01144.x.
We present two rare cases of phacomatosis pigmentovascularis type IIb, with one patient demonstrating concurrent Sturge-Weber syndrome and Klippel-Trenaunay syndrome. To the best of our knowledge, this is the second infantile case meeting diagnostic criteria for systemic phacomatosis pigmentovascularis type IIb, Sturge-Weber syndrome and Klippel-Trenaunay syndrome in the English language literature.
我们报告了两例罕见的IIb型色素血管性母斑病，其中一例患者同时患有斯-韦综合征和克-特综合征。据我们所知，这是英文文献中第二例符合全身性IIb型色素血管性母斑病、斯-韦综合征和克-特综合征诊断标准的婴儿病例。
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