遗传性出血性毛细血管扩张症（伦杜-奥斯勒-韦伯病）的眼部表现。
Ocular manifestations in hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease).
作者信息
Brant A M, Schachat A P, White R I
机构信息
Ocular Oncology Service, Wilmer Ophthalmological Institute, Johns Hopkins Hospital, Baltimore, Maryland 21205.
出版信息
Am J Ophthalmol. 1989 Jun 15;107(6):642-6. doi: 10.1016/0002-9394(89)90261-4.
Although hereditary hemorrhagic telangiectasia is a cause of blood tears from the conjunctival telangiectasias, visual loss from intraocular vascular malformations is a rare complication. We examined 20 patients with hereditary hemorrhagic telangiectasia to determine the prevalence of ocular abnormalities in this disease. Seven patients (35%) had conjunctival telangiectasias and two (10%) had retinal vascular malformations.
尽管遗传性出血性毛细血管扩张症是结膜毛细血管扩张导致血性泪液的一个病因，但眼内血管畸形导致的视力丧失是一种罕见的并发症。我们检查了20例遗传性出血性毛细血管扩张症患者，以确定该疾病眼部异常的患病率。7例患者（35%）有结膜毛细血管扩张，2例（10%）有视网膜血管畸形。
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