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First presentation of pyoderma gangrenosum in a patient with partial immunoglobulin A deficiency

We describe the case of a 58-year-old female with an intensely painful and rapidly enlarging necrotic cutaneous ulcer to the right shin on a background of partial immunoglobulin A deficiency (IgAD). She was seen by various healthcare professionals and managed with upscaling antibiotics for celluliti...

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Autores principales: Demirel, S, Shetty, M, Patel, M, Mahmood, K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019357/
https://www.ncbi.nlm.nih.gov/pubmed/35464105
http://dx.doi.org/10.1177/20542704221086386
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author Demirel, S
Shetty, M
Patel, M
Mahmood, K
author_facet Demirel, S
Shetty, M
Patel, M
Mahmood, K
author_sort Demirel, S
collection PubMed
description We describe the case of a 58-year-old female with an intensely painful and rapidly enlarging necrotic cutaneous ulcer to the right shin on a background of partial immunoglobulin A deficiency (IgAD). She was seen by various healthcare professionals and managed with upscaling antibiotics for cellulitis requiring an inpatient hospital stay. The dermatology team made a clinical diagnosis of ulcerative Pyoderma Gangrenosum (PG) on assessing the patient 13 days post-onset of symptoms. The patient responded dramatically to steroids and oral tetracycline. This case highlights the unusually described association between PG and IgAD as well as the diagnostic challenge seen in patients presenting with PG.
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spelling pubmed-90193572022-04-21 First presentation of pyoderma gangrenosum in a patient with partial immunoglobulin A deficiency Demirel, S Shetty, M Patel, M Mahmood, K JRSM Open Case Report We describe the case of a 58-year-old female with an intensely painful and rapidly enlarging necrotic cutaneous ulcer to the right shin on a background of partial immunoglobulin A deficiency (IgAD). She was seen by various healthcare professionals and managed with upscaling antibiotics for cellulitis requiring an inpatient hospital stay. The dermatology team made a clinical diagnosis of ulcerative Pyoderma Gangrenosum (PG) on assessing the patient 13 days post-onset of symptoms. The patient responded dramatically to steroids and oral tetracycline. This case highlights the unusually described association between PG and IgAD as well as the diagnostic challenge seen in patients presenting with PG. SAGE Publications 2022-04-13 /pmc/articles/PMC9019357/ /pubmed/35464105 http://dx.doi.org/10.1177/20542704221086386 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Demirel, S
Shetty, M
Patel, M
Mahmood, K
First presentation of pyoderma gangrenosum in a patient with partial immunoglobulin A deficiency
title First presentation of pyoderma gangrenosum in a patient with partial immunoglobulin A deficiency
title_full First presentation of pyoderma gangrenosum in a patient with partial immunoglobulin A deficiency
title_fullStr First presentation of pyoderma gangrenosum in a patient with partial immunoglobulin A deficiency
title_full_unstemmed First presentation of pyoderma gangrenosum in a patient with partial immunoglobulin A deficiency
title_short First presentation of pyoderma gangrenosum in a patient with partial immunoglobulin A deficiency
title_sort first presentation of pyoderma gangrenosum in a patient with partial immunoglobulin a deficiency
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019357/
https://www.ncbi.nlm.nih.gov/pubmed/35464105
http://dx.doi.org/10.1177/20542704221086386
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