Combination Venetoclax and Rituximab: A Novel Approach to Gastrointestinal Hemorrhage from Acquired Von Willebrand Syndrome in the Setting of Relapsed Chronic Lymphocytic Leukemia

Heald Jt, Oleszewski Rt
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Abstract

Congenital Von Willebrand Disease (VWD) is the most common bleeding diathesis in humans with a prevalence of one percent in the general population. However, acquired Von Willebrand Syndrome (aVWS) is a rare coagulopathy that has been reported to be associated with numerous conditions and occurs through a variety of mechanisms. In addition to causing bleeding diathesis due to coagulopathy, there is evidence that demonstrates Von Willebrand’s Factor (VWF) deficiency leads to aberrant blood vessel formation. Treatment for this disease is directed at stabilization of associated hemorrhage and correction of underlying etiology. We present the case of a patient with aVWS disease due to relapse of Chronic Lymphocytic Leukemia (CLL) complicated by gastrointestinal hemorrhage from gastric and small bowel angiodysplasia treated with rituximab and venetoclax, previously unreported in the medical literature.
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Venetoclax和Rituximab联合治疗复发性慢性淋巴细胞白血病中获得性血管性血友病综合征胃肠道出血的新方法
先天性血管性血友病(VWD)是人类最常见的出血素质,在普通人群中的患病率为1%。然而,获得性血管性血友病综合征(aVWS)是一种罕见的凝血病,据报道与多种疾病有关,并通过多种机制发生。除了凝血障碍导致出血素质外,有证据表明血管性血友病因子(VWF)缺乏会导致异常血管形成。这种疾病的治疗旨在稳定相关出血并纠正潜在病因。我们报告了一例因慢性淋巴细胞白血病(CLL)复发并伴有胃和小肠血管发育不良胃肠道出血而患有aVWS疾病的患者,该患者接受了利妥昔单抗和venetoclax治疗,此前医学文献中未报道。
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