意义未明的单克隆丙种球蛋白病患者获得性血管性血友病综合征
Acquired von Willebrand syndrome in a patient with monoclonal gammopathy of undetermined significance.
作者信息
Puronen Camille E, Josephson Neil C, Broudy Virginia C
机构信息
Department of Medicine, Harborview Medical Center, Seattle, WA 98104, USA.
出版信息
Blood Coagul Fibrinolysis. 2013 Jun;24(4):430-2. doi: 10.1097/MBC.0b013e32835bfdde.
PMID:23249617
Abstract
Acquired von Willebrand syndrome (AVWS) is a rare bleeding disorder that typically presents as mucocutaneous bleeding in individuals with no personal or family history of bleeding disorder. Here we present a case in which a patient presented with profound epistaxis and was found to have AVWS in the setting of monoclonal gammopathy of undetermined significance (MGUS).
摘要
获得性血管性血友病综合征（AVWS）是一种罕见的出血性疾病，通常表现为无个人或家族出血性疾病史的个体出现黏膜皮肤出血。在此，我们报告一例患者，该患者出现严重鼻出血，在意义未明的单克隆丙种球蛋白病（MGUS）背景下被发现患有AVWS。
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