Cargando…
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...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612776/ https://www.ncbi.nlm.nih.gov/pubmed/34840836 http://dx.doi.org/10.1155/2021/1138329 |
_version_ | 1784603513993560064 |
---|---|
author | Bangolo, Ayrton Waykole, Trupti Niazi, Bilal Sajja, Chandini Akhter, Mahabuba Gupta, Bhavna Elias, Sameh |
author_facet | Bangolo, Ayrton Waykole, Trupti Niazi, Bilal Sajja, Chandini Akhter, Mahabuba Gupta, Bhavna Elias, Sameh |
author_sort | Bangolo, Ayrton |
collection | PubMed |
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 | Online Article Text |
id | pubmed-8612776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-86127762021-11-25 A Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female Bangolo, Ayrton Waykole, Trupti Niazi, Bilal Sajja, Chandini Akhter, Mahabuba Gupta, Bhavna Elias, Sameh Case Rep Hematol Case Report 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. Hindawi 2021-11-17 /pmc/articles/PMC8612776/ /pubmed/34840836 http://dx.doi.org/10.1155/2021/1138329 Text en Copyright © 2021 Ayrton Bangolo et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Bangolo, Ayrton Waykole, Trupti Niazi, Bilal Sajja, Chandini Akhter, Mahabuba Gupta, Bhavna Elias, Sameh A Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female |
title | 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_short | 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 |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612776/ https://www.ncbi.nlm.nih.gov/pubmed/34840836 http://dx.doi.org/10.1155/2021/1138329 |
work_keys_str_mv | AT bangoloayrton ararecauseofacquiredfactorxdeficiencyinan87yearoldfemale AT waykoletrupti ararecauseofacquiredfactorxdeficiencyinan87yearoldfemale AT niazibilal ararecauseofacquiredfactorxdeficiencyinan87yearoldfemale AT sajjachandini ararecauseofacquiredfactorxdeficiencyinan87yearoldfemale AT akhtermahabuba ararecauseofacquiredfactorxdeficiencyinan87yearoldfemale AT guptabhavna ararecauseofacquiredfactorxdeficiencyinan87yearoldfemale AT eliassameh ararecauseofacquiredfactorxdeficiencyinan87yearoldfemale AT bangoloayrton rarecauseofacquiredfactorxdeficiencyinan87yearoldfemale AT waykoletrupti rarecauseofacquiredfactorxdeficiencyinan87yearoldfemale AT niazibilal rarecauseofacquiredfactorxdeficiencyinan87yearoldfemale AT sajjachandini rarecauseofacquiredfactorxdeficiencyinan87yearoldfemale AT akhtermahabuba rarecauseofacquiredfactorxdeficiencyinan87yearoldfemale AT guptabhavna rarecauseofacquiredfactorxdeficiencyinan87yearoldfemale AT eliassameh rarecauseofacquiredfactorxdeficiencyinan87yearoldfemale |