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一位患有多种合并症的患者出现获得性血管性血友病综合征,包括边缘区淋巴瘤伴 IgA 单克隆丙种球蛋白病和高黏滞血症综合征。

Acquired von Willebrand Syndrome in a Patient with Multiple Comorbidities, Including MALT Lymphoma with IgA Monoclonal Gammopathy and Hyperviscosity Syndrome.

机构信息

Department of Hematology, Fukushima Medical University, Japan.

Department of Pulmonary Medicine, Fukushima Medical University, Japan.

出版信息

Intern Med. 2023 Feb 15;62(4):605-611. doi: 10.2169/internalmedicine.9815-22. Epub 2022 Jul 22.

Abstract

Acquired von Willebrand syndrome (aVWS) develops with various underlying diseases. We herein report an individual with aVWS associated with mucosa-associated lymphoid tissue lymphoma in the lungs complicated by hyperviscosity syndrome, Sjögren's syndrome, and hypothyroidism. This patient developed life-threatening hemorrhaging during a lung biopsy despite transfusion of concentrate of plasma-derived VWF/factor VIII. The use of rituximab caused remission of the lymphoma and hyperviscosity syndrome in parallel with the resolution of aVWS. Thus, lymphoma and hyperviscosity might result in aVWS. Invasive procedures with a risk of bleeding should be avoided in individuals with aVWS.

摘要

获得性血管性血友病综合征(aVWS)可由多种基础疾病引起。我们在此报告一例与肺部黏膜相关淋巴组织淋巴瘤相关的 aVWS 病例,该病例并发高黏滞血症综合征、干燥综合征和甲状腺功能减退症。尽管输注了血浆源性 vWF/因子 VIII 浓缩物,但该患者在肺活检时仍发生了危及生命的出血。利妥昔单抗的使用使淋巴瘤和高黏滞血症同时得到缓解,aVWS 也得到了缓解。因此,淋巴瘤和高黏滞血症可能导致 aVWS。患有 aVWS 的个体应避免有出血风险的侵入性操作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3efc/10017253/09f20fdeaf0b/1349-7235-62-0605-g001.jpg

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