Recalcitrant course of bullous pemphigoid indicating coexisting hypereosinophilic syndrome: A case report and literature review

KEY CLINICAL MESSAGE: As dermatologists, we must be aware that even limited localized lesions may signal a life‐threatening condition, for which early diagnosis and treatment can improve the prognosis. ABSTRACT: Bullous pemphigoid is an autoimmune disorder characterized by blister formation. Hypereo...

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Autores principales: Ganji, Raziyeh, Diab, Reem, Mousavi, Farideh, Abdollahimajd, Fahimeh
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/PMC10264926/
https://www.ncbi.nlm.nih.gov/pubmed/37323291
http://dx.doi.org/10.1002/ccr3.7384
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author Ganji, Raziyeh
Diab, Reem
Mousavi, Farideh
Abdollahimajd, Fahimeh
author_facet Ganji, Raziyeh
Diab, Reem
Mousavi, Farideh
Abdollahimajd, Fahimeh
author_sort Ganji, Raziyeh
collection PubMed
description KEY CLINICAL MESSAGE: As dermatologists, we must be aware that even limited localized lesions may signal a life‐threatening condition, for which early diagnosis and treatment can improve the prognosis. ABSTRACT: Bullous pemphigoid is an autoimmune disorder characterized by blister formation. Hypereosinophilic syndrome is a myeloproliferative disorder featuring papules, nodules, urticarial lesions, and blisters. The coexistence of these disorders may highlight the involvement of common molecular and cellular factors. Here, we describe a 16‐year‐old patient with hypereosinophilic syndrome and bullous pemphigoid.
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spelling pubmed-102649262023-06-15 Recalcitrant course of bullous pemphigoid indicating coexisting hypereosinophilic syndrome: A case report and literature review Ganji, Raziyeh Diab, Reem Mousavi, Farideh Abdollahimajd, Fahimeh Clin Case Rep Case Report KEY CLINICAL MESSAGE: As dermatologists, we must be aware that even limited localized lesions may signal a life‐threatening condition, for which early diagnosis and treatment can improve the prognosis. ABSTRACT: Bullous pemphigoid is an autoimmune disorder characterized by blister formation. Hypereosinophilic syndrome is a myeloproliferative disorder featuring papules, nodules, urticarial lesions, and blisters. The coexistence of these disorders may highlight the involvement of common molecular and cellular factors. Here, we describe a 16‐year‐old patient with hypereosinophilic syndrome and bullous pemphigoid. John Wiley and Sons Inc. 2023-06-13 /pmc/articles/PMC10264926/ /pubmed/37323291 http://dx.doi.org/10.1002/ccr3.7384 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
Ganji, Raziyeh
Diab, Reem
Mousavi, Farideh
Abdollahimajd, Fahimeh
Recalcitrant course of bullous pemphigoid indicating coexisting hypereosinophilic syndrome: A case report and literature review
title Recalcitrant course of bullous pemphigoid indicating coexisting hypereosinophilic syndrome: A case report and literature review
title_full Recalcitrant course of bullous pemphigoid indicating coexisting hypereosinophilic syndrome: A case report and literature review
title_fullStr Recalcitrant course of bullous pemphigoid indicating coexisting hypereosinophilic syndrome: A case report and literature review
title_full_unstemmed Recalcitrant course of bullous pemphigoid indicating coexisting hypereosinophilic syndrome: A case report and literature review
title_short Recalcitrant course of bullous pemphigoid indicating coexisting hypereosinophilic syndrome: A case report and literature review
title_sort recalcitrant course of bullous pemphigoid indicating coexisting hypereosinophilic syndrome: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10264926/
https://www.ncbi.nlm.nih.gov/pubmed/37323291
http://dx.doi.org/10.1002/ccr3.7384
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