血管性假血友病是以出血时间延长、血浆因子Ⅷ缺乏及血小板功能异常为特征的常染色体显性遗传的出血性疾病。本文报告一家三人并发血管性假血友病,对诊断作概要讨论: 病例介绍例1:陈×,男,15岁。1964年(2岁)出现出血倾向,唇破流血不止,予缝合及对症处理后方停。继后,出血倾向逐渐加 Vasculogenic hemophilia is an autosomal dominant hemorrhagic disease characterized by prolonged bleeding, plasma factor VIII deficiency, and platelet dysfunction. This article reports a trio of patients with von Willebrand\'s disease, a summary diagnosis of the diagnosis: case introduction Example 1: Chen ×, male, 15 years old. 1964 (2 years old) bleeding tendency, lip bleeding more than to suture and symptomatic treatment after stopping. Followed by gradual increase in bleeding tendency