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获得性血管性血友病综合征与AL淀粉样变性自体干细胞移植后出现的继发性IgM意义未明的单克隆丙种球蛋白病相关。

Acquired von Willebrand Syndrome Associated to Secondary IgM MGUS Emerging after Autologous Stem Cell Transplantation for AL Amyloidosis.

作者信息

Qamar Hina, Lee Adrienne, Valentine Karen, Skeith Leslie, Jimenez-Zepeda Victor H

机构信息

Department of Medicine, University of Alberta, Edmonton, AB, Canada.

Southern Alberta Rare Blood & Bleeding Disorders Comprehensive Care Program, Department of Medicine, Calgary, AB, Canada.

出版信息

Mediterr J Hematol Infect Dis. 2017 May 1;9(1):e2017034. doi: 10.4084/MJHID.2017.034. eCollection 2017.

Abstract

Acquired von Willebrand syndrome (AVWS) is a rare hemorrhagic disorder that occurs in patients with no prior personal or family history of bleeding. Here, we describe a case of AVWS occurring after autologous stem cell transplantation (ASCT). Interestingly, AVWS developed after bortezomib-based induction and conditioning regimens. Recent evidence suggests that the proximity of the bortezomib therapy to the collection of stem cells with consequent depletion of regulatory T cells after the conditioning regimen could explain some of the unusual autoimmune complications reported in patients receiving bortezomib prior to ASCT. In addition, this patient developed a secondary MGUS post-ASCT, which may have also contributed to the AVWS. To the best of our knowledge, this is the first case of post-ASCT AVWS reported. Prospective data is needed to better elucidate the mechanisms by which these unusual complications occur in patients receiving bortezomib prior to ASCT.

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,发生于既往无个人或家族出血史的患者。在此,我们描述一例自体干细胞移植(ASCT)后发生AVWS的病例。有趣的是,AVWS在基于硼替佐米的诱导和预处理方案后出现。近期证据表明,硼替佐米治疗与干细胞采集时间接近,导致预处理方案后调节性T细胞耗竭,这可能解释了在ASCT前接受硼替佐米治疗的患者中报告的一些不寻常的自身免疫并发症。此外,该患者在ASCT后发生了继发性意义未明的单克隆丙种球蛋白病(MGUS),这也可能促成了AVWS。据我们所知,这是首例报道的ASCT后AVWS病例。需要前瞻性数据来更好地阐明在ASCT前接受硼替佐米治疗的患者中发生这些不寻常并发症的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/676b/5419196/4176b0decbe5/mjhid-9-1-e2017034f1.jpg

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