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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Detalles Bibliográficos
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
Descripción
Sumario: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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