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Successful Treatment of Linear IgA Disease and Ulcerative Colitis With Sulfasalazine

Linear IgA disease (LAD) is an uncommon autoimmune blistering disease that has been associated with medications, malignancy, and other autoimmune diseases, such as ulcerative colitis (UC). In this case report, a patient with a history of UC developed characteristic LAD lesions. While dapsone is cons...

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Detalles Bibliográficos
Autores principales: Fletcher, Drew, Patel, Sagar, Motaparthi, Kiran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166405/
https://www.ncbi.nlm.nih.gov/pubmed/37168182
http://dx.doi.org/10.7759/cureus.37210
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author Fletcher, Drew
Patel, Sagar
Motaparthi, Kiran
author_facet Fletcher, Drew
Patel, Sagar
Motaparthi, Kiran
author_sort Fletcher, Drew
collection PubMed
description Linear IgA disease (LAD) is an uncommon autoimmune blistering disease that has been associated with medications, malignancy, and other autoimmune diseases, such as ulcerative colitis (UC). In this case report, a patient with a history of UC developed characteristic LAD lesions. While dapsone is considered first-line therapy for LAD, the treatment team opted for an underutilized, plausibly less toxic, and more simplified treatment regimen with sulfasalazine, successfully utilizing the two distinct actions of sulfasalazine’s components - sulfapyridine and 5-aminosalicylate (5-ASA) - to concurrently treat both the LAD and UC symptoms. The authors discuss the pathophysiology of LAD and UC and expound on the mechanistic theory of their association. Additionally, the pharmacodynamics of sulfasalazine and considerations of its side effect profile are examined.
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spelling pubmed-101664052023-05-09 Successful Treatment of Linear IgA Disease and Ulcerative Colitis With Sulfasalazine Fletcher, Drew Patel, Sagar Motaparthi, Kiran Cureus Dermatology Linear IgA disease (LAD) is an uncommon autoimmune blistering disease that has been associated with medications, malignancy, and other autoimmune diseases, such as ulcerative colitis (UC). In this case report, a patient with a history of UC developed characteristic LAD lesions. While dapsone is considered first-line therapy for LAD, the treatment team opted for an underutilized, plausibly less toxic, and more simplified treatment regimen with sulfasalazine, successfully utilizing the two distinct actions of sulfasalazine’s components - sulfapyridine and 5-aminosalicylate (5-ASA) - to concurrently treat both the LAD and UC symptoms. The authors discuss the pathophysiology of LAD and UC and expound on the mechanistic theory of their association. Additionally, the pharmacodynamics of sulfasalazine and considerations of its side effect profile are examined. Cureus 2023-04-06 /pmc/articles/PMC10166405/ /pubmed/37168182 http://dx.doi.org/10.7759/cureus.37210 Text en Copyright © 2023, Fletcher et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Dermatology
Fletcher, Drew
Patel, Sagar
Motaparthi, Kiran
Successful Treatment of Linear IgA Disease and Ulcerative Colitis With Sulfasalazine
title Successful Treatment of Linear IgA Disease and Ulcerative Colitis With Sulfasalazine
title_full Successful Treatment of Linear IgA Disease and Ulcerative Colitis With Sulfasalazine
title_fullStr Successful Treatment of Linear IgA Disease and Ulcerative Colitis With Sulfasalazine
title_full_unstemmed Successful Treatment of Linear IgA Disease and Ulcerative Colitis With Sulfasalazine
title_short Successful Treatment of Linear IgA Disease and Ulcerative Colitis With Sulfasalazine
title_sort successful treatment of linear iga disease and ulcerative colitis with sulfasalazine
topic Dermatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166405/
https://www.ncbi.nlm.nih.gov/pubmed/37168182
http://dx.doi.org/10.7759/cureus.37210
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