Localized scleroderma with pulmonary arterial hypertension and pulmonary interstitial fibrosis in a patient with positive Th/to antibodies: Case report and review of literature

Morphea is an auto‐immune disease, and its association with other immune‐mediated diseases should not come as a surprise. Dermatologists should be aware of its possible coexistence with severe systemic involvement.

Detalles Bibliográficos
Autores principales: Elinkichari, Dorsaf, Tabka, Mariem, Souissi, Asmahane, Alaoui, Fatimazahra, Chelly, Ines, Haouet, Slim, Mokni, Mourad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10188899/
https://www.ncbi.nlm.nih.gov/pubmed/37207083
http://dx.doi.org/10.1002/ccr3.7183
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author Elinkichari, Dorsaf
Tabka, Mariem
Souissi, Asmahane
Alaoui, Fatimazahra
Chelly, Ines
Haouet, Slim
Mokni, Mourad
author_facet Elinkichari, Dorsaf
Tabka, Mariem
Souissi, Asmahane
Alaoui, Fatimazahra
Chelly, Ines
Haouet, Slim
Mokni, Mourad
author_sort Elinkichari, Dorsaf
collection PubMed
description Morphea is an auto‐immune disease, and its association with other immune‐mediated diseases should not come as a surprise. Dermatologists should be aware of its possible coexistence with severe systemic involvement.
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spelling pubmed-101888992023-05-18 Localized scleroderma with pulmonary arterial hypertension and pulmonary interstitial fibrosis in a patient with positive Th/to antibodies: Case report and review of literature Elinkichari, Dorsaf Tabka, Mariem Souissi, Asmahane Alaoui, Fatimazahra Chelly, Ines Haouet, Slim Mokni, Mourad Clin Case Rep Case Report Morphea is an auto‐immune disease, and its association with other immune‐mediated diseases should not come as a surprise. Dermatologists should be aware of its possible coexistence with severe systemic involvement. John Wiley and Sons Inc. 2023-05-16 /pmc/articles/PMC10188899/ /pubmed/37207083 http://dx.doi.org/10.1002/ccr3.7183 Text en © 2023 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
Elinkichari, Dorsaf
Tabka, Mariem
Souissi, Asmahane
Alaoui, Fatimazahra
Chelly, Ines
Haouet, Slim
Mokni, Mourad
Localized scleroderma with pulmonary arterial hypertension and pulmonary interstitial fibrosis in a patient with positive Th/to antibodies: Case report and review of literature
title Localized scleroderma with pulmonary arterial hypertension and pulmonary interstitial fibrosis in a patient with positive Th/to antibodies: Case report and review of literature
title_full Localized scleroderma with pulmonary arterial hypertension and pulmonary interstitial fibrosis in a patient with positive Th/to antibodies: Case report and review of literature
title_fullStr Localized scleroderma with pulmonary arterial hypertension and pulmonary interstitial fibrosis in a patient with positive Th/to antibodies: Case report and review of literature
title_full_unstemmed Localized scleroderma with pulmonary arterial hypertension and pulmonary interstitial fibrosis in a patient with positive Th/to antibodies: Case report and review of literature
title_short Localized scleroderma with pulmonary arterial hypertension and pulmonary interstitial fibrosis in a patient with positive Th/to antibodies: Case report and review of literature
title_sort localized scleroderma with pulmonary arterial hypertension and pulmonary interstitial fibrosis in a patient with positive th/to antibodies: case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10188899/
https://www.ncbi.nlm.nih.gov/pubmed/37207083
http://dx.doi.org/10.1002/ccr3.7183
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