Excellent response to rituximab in a patient with recalcitrant epidermolysis bullosa acquisita: a case report

Epidermolysis Bullosa Acquisita is a rare, chronic autoimmune blistering disorder characterized by vesicles and bullae on the skin and mucous membranes. This condition, presenting typically in adulthood, is caused by autoantibodies against type VII collagen. Conventional treatments, including system...

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Main Authors: Fahad Alrashidi, Khalid Nabil Nagshabandi, Ruaa Alharithy
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2025-05-01
Series:Journal of the Egyptian Women’s Dermatologic Society
Subjects:
Online Access:https://journals.lww.com/10.4103/jewd.jewd_109_24
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author Fahad Alrashidi
Khalid Nabil Nagshabandi
Ruaa Alharithy
author_facet Fahad Alrashidi
Khalid Nabil Nagshabandi
Ruaa Alharithy
author_sort Fahad Alrashidi
collection DOAJ
description Epidermolysis Bullosa Acquisita is a rare, chronic autoimmune blistering disorder characterized by vesicles and bullae on the skin and mucous membranes. This condition, presenting typically in adulthood, is caused by autoantibodies against type VII collagen. Conventional treatments, including systemic corticosteroids and immunosuppressants, often fail to achieve long-term remission. Biologic agents like rituximab have shown promise in managing refractory cases. This report presents a case of a 27-year-old female with recalcitrant epidermolysis bullosa acquisita successfully managed after starting rituximab therapy.
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publisher Wolters Kluwer Medknow Publications
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series Journal of the Egyptian Women’s Dermatologic Society
spelling doaj-art-ecfaeebc69bd455a97f250451bedd7a72025-08-20T02:32:29ZengWolters Kluwer Medknow PublicationsJournal of the Egyptian Women’s Dermatologic Society2090-25652025-05-0122217017410.4103/jewd.jewd_109_24Excellent response to rituximab in a patient with recalcitrant epidermolysis bullosa acquisita: a case reportFahad AlrashidiKhalid Nabil NagshabandiRuaa AlharithyEpidermolysis Bullosa Acquisita is a rare, chronic autoimmune blistering disorder characterized by vesicles and bullae on the skin and mucous membranes. This condition, presenting typically in adulthood, is caused by autoantibodies against type VII collagen. Conventional treatments, including systemic corticosteroids and immunosuppressants, often fail to achieve long-term remission. Biologic agents like rituximab have shown promise in managing refractory cases. This report presents a case of a 27-year-old female with recalcitrant epidermolysis bullosa acquisita successfully managed after starting rituximab therapy.https://journals.lww.com/10.4103/jewd.jewd_109_24biologicsepidermolysis bullosa acquisitarituximab
spellingShingle Fahad Alrashidi
Khalid Nabil Nagshabandi
Ruaa Alharithy
Excellent response to rituximab in a patient with recalcitrant epidermolysis bullosa acquisita: a case report
Journal of the Egyptian Women’s Dermatologic Society
biologics
epidermolysis bullosa acquisita
rituximab
title Excellent response to rituximab in a patient with recalcitrant epidermolysis bullosa acquisita: a case report
title_full Excellent response to rituximab in a patient with recalcitrant epidermolysis bullosa acquisita: a case report
title_fullStr Excellent response to rituximab in a patient with recalcitrant epidermolysis bullosa acquisita: a case report
title_full_unstemmed Excellent response to rituximab in a patient with recalcitrant epidermolysis bullosa acquisita: a case report
title_short Excellent response to rituximab in a patient with recalcitrant epidermolysis bullosa acquisita: a case report
title_sort excellent response to rituximab in a patient with recalcitrant epidermolysis bullosa acquisita a case report
topic biologics
epidermolysis bullosa acquisita
rituximab
url https://journals.lww.com/10.4103/jewd.jewd_109_24
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AT ruaaalharithy excellentresponsetorituximabinapatientwithrecalcitrantepidermolysisbullosaacquisitaacasereport