A Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female

Factor X deficiency is a rare coagulopathy that can be inherited or acquired. Acquired factor X deficiency has been associated with plasma cell dyscrasias, amyloids, and use of vitamin K antagonists. Of plasma cell dyscrasias, most cases in the literature have been associated with multiple myeloma w...

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Autores principales: Ayrton Bangolo, Trupti Waykole, Bilal Niazi, Chandini Sajja, Mahabuba Akhter, Bhavna Gupta, Sameh Elias
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Publicado: Hindawi Limited 2021
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Acceso en línea:https://doaj.org/article/48c74ffb87a4442a915979db976bd1e5
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spelling oai:doaj.org-article:48c74ffb87a4442a915979db976bd1e52021-11-29T00:55:40ZA Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female2090-657910.1155/2021/1138329https://doaj.org/article/48c74ffb87a4442a915979db976bd1e52021-01-01T00:00:00Zhttp://dx.doi.org/10.1155/2021/1138329https://doaj.org/toc/2090-6579Factor X deficiency is a rare coagulopathy that can be inherited or acquired. Acquired factor X deficiency has been associated with plasma cell dyscrasias, amyloids, and use of vitamin K antagonists. Of plasma cell dyscrasias, most cases in the literature have been associated with multiple myeloma with or without concomitant AL amyloidosis. Here, we present a rare case of acquired isolated factor X deficiency in an elderly patient with immunoglobulin A (Ig A) monoclonal gammopathy of undetermined significance (MGUS). Herein, we highlight a rare cause of acquired factor X deficiency, and we hope to contribute to the growing literature of plasma cell dyscrasias associated with factor X deficiency.Ayrton BangoloTrupti WaykoleBilal NiaziChandini SajjaMahabuba AkhterBhavna GuptaSameh EliasHindawi LimitedarticleDiseases of the blood and blood-forming organsRC633-647.5ENCase Reports in Hematology, Vol 2021 (2021)
institution DOAJ
collection DOAJ
language EN
topic Diseases of the blood and blood-forming organs
RC633-647.5
spellingShingle Diseases of the blood and blood-forming organs
RC633-647.5
Ayrton Bangolo
Trupti Waykole
Bilal Niazi
Chandini Sajja
Mahabuba Akhter
Bhavna Gupta
Sameh Elias
A Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female
description Factor X deficiency is a rare coagulopathy that can be inherited or acquired. Acquired factor X deficiency has been associated with plasma cell dyscrasias, amyloids, and use of vitamin K antagonists. Of plasma cell dyscrasias, most cases in the literature have been associated with multiple myeloma with or without concomitant AL amyloidosis. Here, we present a rare case of acquired isolated factor X deficiency in an elderly patient with immunoglobulin A (Ig A) monoclonal gammopathy of undetermined significance (MGUS). Herein, we highlight a rare cause of acquired factor X deficiency, and we hope to contribute to the growing literature of plasma cell dyscrasias associated with factor X deficiency.
format article
author Ayrton Bangolo
Trupti Waykole
Bilal Niazi
Chandini Sajja
Mahabuba Akhter
Bhavna Gupta
Sameh Elias
author_facet Ayrton Bangolo
Trupti Waykole
Bilal Niazi
Chandini Sajja
Mahabuba Akhter
Bhavna Gupta
Sameh Elias
author_sort Ayrton Bangolo
title A Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female
title_short A Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female
title_full A Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female
title_fullStr A Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female
title_full_unstemmed A Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female
title_sort rare cause of acquired factor x deficiency in an 87-year-old female
publisher Hindawi Limited
publishDate 2021
url https://doaj.org/article/48c74ffb87a4442a915979db976bd1e5
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