一名17岁原发性血小板增多症患者获得性血管性血友病综合征：病例报告及文献复习
Acquired von Willebrand Syndrome in a 17-Year-Old With Essential Thrombocythemia: A Case Report With Literature Review.
作者信息
Youn Linda, Kuta Amber, Srinivasan Mirra, Mahatara Renuka, Khalil Mazen
机构信息
Internal Medicine, St. Bernards Medical Center, Jonesboro, USA.
Internal Medicine, New York Institute of Technology College of Osteopathic Medicine, Jonesboro, USA.
出版信息
Cureus. 2024 Mar 6;16(3):e55668. doi: 10.7759/cureus.55668. eCollection 2024 Mar.
Acquired von Willebrand syndrome (AVWS) is a rare bleeding disorder that is often underdiagnosed. AVWS typically occurs in adults without a family history of bleeding disorders and with associated conditions such as lymphoproliferative, myeloproliferative, and cardiovascular disorders. Here, we present a case of AVWS in a young patient with essential thrombocythemia and a literature review on AVWS in the setting of essential thrombocythemia.
获得性血管性血友病综合征（AVWS）是一种罕见的出血性疾病，常常未被诊断出来。AVWS通常发生在没有出血性疾病家族史且伴有如淋巴增殖性、骨髓增殖性和心血管疾病等相关病症的成年人中。在此，我们报告一例患有原发性血小板增多症的年轻患者的AVWS病例，并对原发性血小板增多症背景下的AVWS进行文献综述。
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