Acquired von Willebrand syndrome and lymphoproliferative disorders: A case report

Acquired von Willebrand syndrome is a rare bleeding disorder often secondary to an underlying lymphoproliferative disorder. We report a case in whom response of both the acquired von Willebrand syndrome and smoldering multiple myeloma persist 14 months after daratumumab treatment discontinuation.

Detalles Bibliográficos
Autores principales: Nicol, Christophe, Raj, Leela, Guillerm, Gaëlle, Couturaud, Francis, Eveillard, Jean‐Richard, Pan‐Petesch, Brigitte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250994/
https://www.ncbi.nlm.nih.gov/pubmed/32477542
http://dx.doi.org/10.1002/ccr3.2770
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author Nicol, Christophe
Raj, Leela
Guillerm, Gaëlle
Couturaud, Francis
Eveillard, Jean‐Richard
Pan‐Petesch, Brigitte
author_facet Nicol, Christophe
Raj, Leela
Guillerm, Gaëlle
Couturaud, Francis
Eveillard, Jean‐Richard
Pan‐Petesch, Brigitte
author_sort Nicol, Christophe
collection PubMed
description Acquired von Willebrand syndrome is a rare bleeding disorder often secondary to an underlying lymphoproliferative disorder. We report a case in whom response of both the acquired von Willebrand syndrome and smoldering multiple myeloma persist 14 months after daratumumab treatment discontinuation.
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spelling pubmed-72509942020-05-29 Acquired von Willebrand syndrome and lymphoproliferative disorders: A case report Nicol, Christophe Raj, Leela Guillerm, Gaëlle Couturaud, Francis Eveillard, Jean‐Richard Pan‐Petesch, Brigitte Clin Case Rep Case Reports Acquired von Willebrand syndrome is a rare bleeding disorder often secondary to an underlying lymphoproliferative disorder. We report a case in whom response of both the acquired von Willebrand syndrome and smoldering multiple myeloma persist 14 months after daratumumab treatment discontinuation. John Wiley and Sons Inc. 2020-03-09 /pmc/articles/PMC7250994/ /pubmed/32477542 http://dx.doi.org/10.1002/ccr3.2770 Text en © 2020 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Nicol, Christophe
Raj, Leela
Guillerm, Gaëlle
Couturaud, Francis
Eveillard, Jean‐Richard
Pan‐Petesch, Brigitte
Acquired von Willebrand syndrome and lymphoproliferative disorders: A case report
title Acquired von Willebrand syndrome and lymphoproliferative disorders: A case report
title_full Acquired von Willebrand syndrome and lymphoproliferative disorders: A case report
title_fullStr Acquired von Willebrand syndrome and lymphoproliferative disorders: A case report
title_full_unstemmed Acquired von Willebrand syndrome and lymphoproliferative disorders: A case report
title_short Acquired von Willebrand syndrome and lymphoproliferative disorders: A case report
title_sort acquired von willebrand syndrome and lymphoproliferative disorders: a case report
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250994/
https://www.ncbi.nlm.nih.gov/pubmed/32477542
http://dx.doi.org/10.1002/ccr3.2770
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