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Acquired von Willebrand Syndrome in a Patient with Multiple Comorbidities, Including MALT Lymphoma with IgA Monoclonal Gammopathy and Hyperviscosity Syndrome
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 develo...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japanese Society of Internal Medicine
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017253/ https://www.ncbi.nlm.nih.gov/pubmed/35871597 http://dx.doi.org/10.2169/internalmedicine.9815-22 |
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author | Owari, Mai Harada-Shirado, Kayo Togawa, Ryuichi Fukatsu, Masahiko Sato, Yuki Fukuchi, Koichiro Endo, Mamiko Takahashi, Hiroshi Kimura, Satoshi Osaki, Tsukasa Souri, Masayoshi Ichinose, Akitada Shibata, Yoko Hashimoto, Yuko Ikezoe, Takayuki |
author_facet | Owari, Mai Harada-Shirado, Kayo Togawa, Ryuichi Fukatsu, Masahiko Sato, Yuki Fukuchi, Koichiro Endo, Mamiko Takahashi, Hiroshi Kimura, Satoshi Osaki, Tsukasa Souri, Masayoshi Ichinose, Akitada Shibata, Yoko Hashimoto, Yuko Ikezoe, Takayuki |
author_sort | Owari, Mai |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10017253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Japanese Society of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-100172532023-03-16 Acquired von Willebrand Syndrome in a Patient with Multiple Comorbidities, Including MALT Lymphoma with IgA Monoclonal Gammopathy and Hyperviscosity Syndrome Owari, Mai Harada-Shirado, Kayo Togawa, Ryuichi Fukatsu, Masahiko Sato, Yuki Fukuchi, Koichiro Endo, Mamiko Takahashi, Hiroshi Kimura, Satoshi Osaki, Tsukasa Souri, Masayoshi Ichinose, Akitada Shibata, Yoko Hashimoto, Yuko Ikezoe, Takayuki Intern Med Case Report 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. The Japanese Society of Internal Medicine 2022-07-22 2023-02-15 /pmc/articles/PMC10017253/ /pubmed/35871597 http://dx.doi.org/10.2169/internalmedicine.9815-22 Text en Copyright © 2023 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Owari, Mai Harada-Shirado, Kayo Togawa, Ryuichi Fukatsu, Masahiko Sato, Yuki Fukuchi, Koichiro Endo, Mamiko Takahashi, Hiroshi Kimura, Satoshi Osaki, Tsukasa Souri, Masayoshi Ichinose, Akitada Shibata, Yoko Hashimoto, Yuko Ikezoe, Takayuki Acquired von Willebrand Syndrome in a Patient with Multiple Comorbidities, Including MALT Lymphoma with IgA Monoclonal Gammopathy and Hyperviscosity Syndrome |
title | Acquired von Willebrand Syndrome in a Patient with Multiple Comorbidities, Including MALT Lymphoma with IgA Monoclonal Gammopathy and Hyperviscosity Syndrome |
title_full | Acquired von Willebrand Syndrome in a Patient with Multiple Comorbidities, Including MALT Lymphoma with IgA Monoclonal Gammopathy and Hyperviscosity Syndrome |
title_fullStr | Acquired von Willebrand Syndrome in a Patient with Multiple Comorbidities, Including MALT Lymphoma with IgA Monoclonal Gammopathy and Hyperviscosity Syndrome |
title_full_unstemmed | Acquired von Willebrand Syndrome in a Patient with Multiple Comorbidities, Including MALT Lymphoma with IgA Monoclonal Gammopathy and Hyperviscosity Syndrome |
title_short | Acquired von Willebrand Syndrome in a Patient with Multiple Comorbidities, Including MALT Lymphoma with IgA Monoclonal Gammopathy and Hyperviscosity Syndrome |
title_sort | acquired von willebrand syndrome in a patient with multiple comorbidities, including malt lymphoma with iga monoclonal gammopathy and hyperviscosity syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017253/ https://www.ncbi.nlm.nih.gov/pubmed/35871597 http://dx.doi.org/10.2169/internalmedicine.9815-22 |
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