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A striking presentation of pustular Sweet syndrome induced by trimethoprim‐sulfamethoxazole
We describe a strikingly robust presentation of trimethoprim‐sulfamethoxazole (TMP‐SMX)‐induced pustular Sweet syndrome and discuss how to distinguish it from iododerma and other neutrophil‐rich conditions. A review of the literature indicates that TMP‐SMX‐induced Sweet syndrome (SS) may have higher...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796284/ https://www.ncbi.nlm.nih.gov/pubmed/35866718 http://dx.doi.org/10.1111/ajd.13897 |
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author | Ryder, C. Yoonhee Matthews, Natalie H. Lowe, Lori Wang, Frank |
author_facet | Ryder, C. Yoonhee Matthews, Natalie H. Lowe, Lori Wang, Frank |
author_sort | Ryder, C. Yoonhee |
collection | PubMed |
description | We describe a strikingly robust presentation of trimethoprim‐sulfamethoxazole (TMP‐SMX)‐induced pustular Sweet syndrome and discuss how to distinguish it from iododerma and other neutrophil‐rich conditions. A review of the literature indicates that TMP‐SMX‐induced Sweet syndrome (SS) may have higher rates of neutrophilia and greater ocular, mucosal, and musculoskeletal involvement compared to SS from other drugs. Recognizing these features and identifying the offending agent are critical for correctly diagnosing TMP‐SMX‐induced SS in a timely manner. |
format | Online Article Text |
id | pubmed-9796284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97962842022-12-30 A striking presentation of pustular Sweet syndrome induced by trimethoprim‐sulfamethoxazole Ryder, C. Yoonhee Matthews, Natalie H. Lowe, Lori Wang, Frank Australas J Dermatol Brief Reports We describe a strikingly robust presentation of trimethoprim‐sulfamethoxazole (TMP‐SMX)‐induced pustular Sweet syndrome and discuss how to distinguish it from iododerma and other neutrophil‐rich conditions. A review of the literature indicates that TMP‐SMX‐induced Sweet syndrome (SS) may have higher rates of neutrophilia and greater ocular, mucosal, and musculoskeletal involvement compared to SS from other drugs. Recognizing these features and identifying the offending agent are critical for correctly diagnosing TMP‐SMX‐induced SS in a timely manner. John Wiley and Sons Inc. 2022-07-22 2022-11 /pmc/articles/PMC9796284/ /pubmed/35866718 http://dx.doi.org/10.1111/ajd.13897 Text en © 2022 The Authors. Australasian Journal of Dermatology published by John Wiley & Sons Australia, Ltd on behalf of Australasian College of Dermatologists. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Brief Reports Ryder, C. Yoonhee Matthews, Natalie H. Lowe, Lori Wang, Frank A striking presentation of pustular Sweet syndrome induced by trimethoprim‐sulfamethoxazole |
title | A striking presentation of pustular Sweet syndrome induced by trimethoprim‐sulfamethoxazole |
title_full | A striking presentation of pustular Sweet syndrome induced by trimethoprim‐sulfamethoxazole |
title_fullStr | A striking presentation of pustular Sweet syndrome induced by trimethoprim‐sulfamethoxazole |
title_full_unstemmed | A striking presentation of pustular Sweet syndrome induced by trimethoprim‐sulfamethoxazole |
title_short | A striking presentation of pustular Sweet syndrome induced by trimethoprim‐sulfamethoxazole |
title_sort | striking presentation of pustular sweet syndrome induced by trimethoprim‐sulfamethoxazole |
topic | Brief Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796284/ https://www.ncbi.nlm.nih.gov/pubmed/35866718 http://dx.doi.org/10.1111/ajd.13897 |
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