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Neutrophilic dermatoses in a seronegative rheumatoid arthritis patient: A case report

Rheumatoid arthritis (RA) is a chronic inflammatory disease, characterized by symmetric and destructive polyarthritis with a broad‐spectrum clinical manifestation of various organs. RND is an unusual distinctive manifestation of RA and typically develops in severe RA. This report aims to present an...

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Autores principales: IbnIdris Rodwan, Amel Awad, A. Mohammed, Abdel Gaffar., Adam Essa, Mohammed Elmujtba, Abdalla Babker, Atif Elhadi, Mohamed Abdelsatir, Ali, Mohammed Elagib, Elnour
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741871/
https://www.ncbi.nlm.nih.gov/pubmed/35028144
http://dx.doi.org/10.1002/ccr3.5249
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author IbnIdris Rodwan, Amel Awad
A. Mohammed, Abdel Gaffar.
Adam Essa, Mohammed Elmujtba
Abdalla Babker, Atif Elhadi
Mohamed Abdelsatir, Ali
Mohammed Elagib, Elnour
author_facet IbnIdris Rodwan, Amel Awad
A. Mohammed, Abdel Gaffar.
Adam Essa, Mohammed Elmujtba
Abdalla Babker, Atif Elhadi
Mohamed Abdelsatir, Ali
Mohammed Elagib, Elnour
author_sort IbnIdris Rodwan, Amel Awad
collection PubMed
description Rheumatoid arthritis (RA) is a chronic inflammatory disease, characterized by symmetric and destructive polyarthritis with a broad‐spectrum clinical manifestation of various organs. RND is an unusual distinctive manifestation of RA and typically develops in severe RA. This report aims to present an unusual and a rare neutrophilic skin condition, in a seronegative RA Sudanese patient. A 51‐year‐old woman was diagnosed with RA three years ago and a history of bilateral polyarthritis, presented with a skin rash involving her extremities and abdomen. Clinical examination of her skin revealed the presence of maculopapular lesions affecting the extensor surfaces of the lower extremities and the lower part of the abdomen with hyperpigmentation. Hand X‐ray demonstrated periarticular osteopenia, and laboratory and immunological studies that include C‐reactive protein, erythrocyte sedimentation rate (ESR), rheumatoid factor (RF), anticitrullinated peptide antibodies (ACPAs), and antinuclear factor in addition to skin biopsy were all suggested a diagnosis of neutrophilic dermatosis. The patient received steroids for the skin lesion still no significant improvement was seen, and then, cyclosporin 100 mg was administrated twice/ day with close monitoring, and two weeks later marked improvement was shown.
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spelling pubmed-87418712022-01-12 Neutrophilic dermatoses in a seronegative rheumatoid arthritis patient: A case report IbnIdris Rodwan, Amel Awad A. Mohammed, Abdel Gaffar. Adam Essa, Mohammed Elmujtba Abdalla Babker, Atif Elhadi Mohamed Abdelsatir, Ali Mohammed Elagib, Elnour Clin Case Rep Case Report Rheumatoid arthritis (RA) is a chronic inflammatory disease, characterized by symmetric and destructive polyarthritis with a broad‐spectrum clinical manifestation of various organs. RND is an unusual distinctive manifestation of RA and typically develops in severe RA. This report aims to present an unusual and a rare neutrophilic skin condition, in a seronegative RA Sudanese patient. A 51‐year‐old woman was diagnosed with RA three years ago and a history of bilateral polyarthritis, presented with a skin rash involving her extremities and abdomen. Clinical examination of her skin revealed the presence of maculopapular lesions affecting the extensor surfaces of the lower extremities and the lower part of the abdomen with hyperpigmentation. Hand X‐ray demonstrated periarticular osteopenia, and laboratory and immunological studies that include C‐reactive protein, erythrocyte sedimentation rate (ESR), rheumatoid factor (RF), anticitrullinated peptide antibodies (ACPAs), and antinuclear factor in addition to skin biopsy were all suggested a diagnosis of neutrophilic dermatosis. The patient received steroids for the skin lesion still no significant improvement was seen, and then, cyclosporin 100 mg was administrated twice/ day with close monitoring, and two weeks later marked improvement was shown. John Wiley and Sons Inc. 2022-01-07 /pmc/articles/PMC8741871/ /pubmed/35028144 http://dx.doi.org/10.1002/ccr3.5249 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. 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 Case Report
IbnIdris Rodwan, Amel Awad
A. Mohammed, Abdel Gaffar.
Adam Essa, Mohammed Elmujtba
Abdalla Babker, Atif Elhadi
Mohamed Abdelsatir, Ali
Mohammed Elagib, Elnour
Neutrophilic dermatoses in a seronegative rheumatoid arthritis patient: A case report
title Neutrophilic dermatoses in a seronegative rheumatoid arthritis patient: A case report
title_full Neutrophilic dermatoses in a seronegative rheumatoid arthritis patient: A case report
title_fullStr Neutrophilic dermatoses in a seronegative rheumatoid arthritis patient: A case report
title_full_unstemmed Neutrophilic dermatoses in a seronegative rheumatoid arthritis patient: A case report
title_short Neutrophilic dermatoses in a seronegative rheumatoid arthritis patient: A case report
title_sort neutrophilic dermatoses in a seronegative rheumatoid arthritis patient: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741871/
https://www.ncbi.nlm.nih.gov/pubmed/35028144
http://dx.doi.org/10.1002/ccr3.5249
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