Acquired von Willebrand Syndrome Associated with a Smoldering Multiple Myeloma, Successfully Treated by Daratumumab, Lenalidomide, and Dexamethasone.

IF 1.7 4区 医学 Q3 HEMATOLOGY
Acta Haematologica Pub Date : 2024-01-01 Epub Date: 2024-02-15 DOI:10.1159/000536650
Michael Iarossi, Marie-Christiane Madeleine Vekemans, Nicolas Weynants, Cedric Hermans
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引用次数: 0

Abstract

Introduction: Acquired von Willebrand syndrome (AvWS) is a rare entity with approximately 700 cases described in the literature. A number of etiologies are responsible for this condition, mainly lymphoproliferative, myeloproliferative syndromes and cardiac diseases. Management is aimed at preventing and treating bleeds, as well as treating the underlying pathology. In the case of a monoclonal gammopathy, there are limited evidence and high heterogeneity only based on old case reports, resulting in poor quality recommendations. It seems essential in 2023 to take into account and offer the new anti-myeloma treatments available.

Case presentation: We describe the case of a patient with an AvWS secondary to an IgG smoldering multiple myeloma, experiencing multiple bleeding, treated successfully with daratumumab, lenalidomide, and dexamethasone, after multiple treatment failure.

Conclusion: Daratumumab, lenalidomide, and dexamethasone was demonstrated as a rapid and effective treatment for a patient with severe AvWS and multiple bleeding complications.

达拉单抗、来那度胺和地塞米松成功治疗了伴有多发性骨髓瘤的获得性冯-威廉综合征。
简介获得性冯-威廉综合征(AvWS)是一种罕见病,文献中描述的病例约有 700 例。导致这种病症的病因有很多,主要是淋巴增生、骨髓增生综合征和心脏病。治疗的目的是预防和治疗出血,以及治疗潜在的病变。就单克隆抗体病而言,目前的证据有限,且异质性较高,仅基于旧的病例报告,因此建议的质量不高。在2023年,考虑并提供现有的抗骨髓瘤新疗法似乎至关重要:我们描述了一例继发于 IgG 多发性骨髓瘤的 AvWS 患者的病例,该患者经历了多次出血,在多次治疗失败后,使用达拉单抗、来那度胺和地塞米松成功治疗:结论:达拉单抗、来那度胺和地塞米松是治疗严重AvWS和多发性出血并发症患者的快速有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Haematologica
Acta Haematologica 医学-血液学
CiteScore
4.90
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: ''Acta Haematologica'' is a well-established and internationally recognized clinically-oriented journal featuring balanced, wide-ranging coverage of current hematology research. A wealth of information on such problems as anemia, leukemia, lymphoma, multiple myeloma, hereditary disorders, blood coagulation, growth factors, hematopoiesis and differentiation is contained in first-rate basic and clinical papers some of which are accompanied by editorial comments by eminent experts. These are supplemented by short state-of-the-art communications, reviews and correspondence as well as occasional special issues devoted to ‘hot topics’ in hematology. These will keep the practicing hematologist well informed of the new developments in the field.
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