Humphries J E, Frierson H F, Underwood P B
Department of Pathology, University of Virginia Health Sciences Center, Charlottesville.
Obstet Gynecol. 1993 May;81(5 ( Pt 2)):865-6.
The Osler-Weber-Rendu syndrome (hereditary hemorrhagic telangiectasia) is an autosomal dominant disorder of blood vessels associated with mucocutaneous telangiectasis and arteriovenous malformations of internal organs.
A 23-year-old woman was found on routine gynecologic examination to have asymptomatic vaginal telangiectasias, a previously unreported initial site of involvement in this syndrome.
The finding of asymptomatic vaginal telangiectasias on routine pelvic examination should alert the clinician to the possibility of the Osler-Weber-Rendu syndrome.
奥斯勒-韦伯-伦杜综合征（遗传性出血性毛细血管扩张症）是一种常染色体显性血管疾病，与黏膜皮肤毛细血管扩张及内脏动静脉畸形相关。
一名23岁女性在常规妇科检查中被发现有无症状性阴道毛细血管扩张，这是该综合征此前未报道过的初始受累部位。
在常规盆腔检查中发现无症状性阴道毛细血管扩张应提醒临床医生注意奥斯勒-韦伯-伦杜综合征的可能性。
