[1型神经纤维瘤病患儿的视网膜缺血性病变]
[Ischemic lesions of the retina in a child with neurofibromatosis 1].
作者信息
Mosin I M
出版信息
Vestn Oftalmol. 1998 May-Jun;114(3):46-8.
PMID:9720403
Abstract
A rare case is described: unilateral diffuse retinal ischemia in a 3-year-old girl with type I neurofibromatosis. Besides retinal involvement, the child developed melanocytic iridial hamartomas in the ipsilateral eye and skin disorders presenting as "milk-and-coffee" spots and freckles in the armpits. Differential diagnosis and pathogenesis of retinal ischemia in neurofibromatosis are discussed.
摘要
描述了一例罕见病例
一名患有I型神经纤维瘤病的3岁女孩出现单侧弥漫性视网膜缺血。除视网膜受累外，该患儿同侧眼还出现了黑素细胞性虹膜错构瘤，以及表现为“牛奶咖啡斑”和腋窝雀斑的皮肤病变。讨论了神经纤维瘤病中视网膜缺血的鉴别诊断和发病机制。
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