IVa型色素血管性斑痣性错构瘤病
Phakomatosis pigmentovascularis type IVa.
作者信息
Hasegawa Y, Yasuhara M
出版信息
Arch Dermatol. 1985 May;121(5):651-5.
PMID:3994413
Abstract
Phakomatosis pigmentovascularis was first reported in 1947. We describe a 1-year-old Japanese girl who, since birth, has had three nevoid skin disorders: nevus flammeus, nevus spilus, and aberrant mongolian spots. No systemic disease of any kind has been present. We believe that this phakomatosis, which we have named phakomatosis pigmentovascularis type IVa, does not reflect the merely coincidental coexistence of three kinds of nevi.
摘要
色素血管性斑痣性错构瘤病于1947年首次被报道。我们描述了一名1岁的日本女孩，自出生以来患有三种痣样皮肤疾病：火焰状痣、斑状痣和异常蒙古斑。未出现任何全身性疾病。我们认为这种斑痣性错构瘤病（我们将其命名为IVa型色素血管性斑痣性错构瘤病）并非仅仅是三种痣的偶然并存。
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