A Case of Bullous Skin Disease Presenting with Odynophagia: A Diagnostic Challenge

We report a case of Epidermolysis Bullosa Acquisita (EBA) that presented as a diagnostic challenge. A 60-year-old Qatari lady presented with odynophagia, oral ulceration, and weight loss. Multiple physicians investigated her for over 6 months with a multitude of tests and serial gastroscopies, all o...

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Main Authors: G. Kravvas, D. Veitch, C. M. Perrett
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Case Reports in Dermatological Medicine
Online Access:http://dx.doi.org/10.1155/2016/2839104
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author G. Kravvas
D. Veitch
C. M. Perrett
author_facet G. Kravvas
D. Veitch
C. M. Perrett
author_sort G. Kravvas
collection DOAJ
description We report a case of Epidermolysis Bullosa Acquisita (EBA) that presented as a diagnostic challenge. A 60-year-old Qatari lady presented with odynophagia, oral ulceration, and weight loss. Multiple physicians investigated her for over 6 months with a multitude of tests and serial gastroscopies, all of which failed to reach a conclusive diagnosis. Only after referral to a dermatologist and full body examination was diagnosis finally achieved. After reviewing the literature, we provide a summary of EBA and highlight the importance of comprehensive clinical reviews in order to avoid unnecessary morbidity.
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institution Kabale University
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spelling doaj-art-5863e282dae24ab79cfea3839191102c2025-08-20T03:33:36ZengWileyCase Reports in Dermatological Medicine2090-64632090-64712016-01-01201610.1155/2016/28391042839104A Case of Bullous Skin Disease Presenting with Odynophagia: A Diagnostic ChallengeG. Kravvas0D. Veitch1C. M. Perrett2Department of Dermatology, University College London Hospitals, London NW1 2BU, UKDepartment of Dermatology, University College London Hospitals, London NW1 2BU, UKDepartment of Dermatology, University College London Hospitals, London NW1 2BU, UKWe report a case of Epidermolysis Bullosa Acquisita (EBA) that presented as a diagnostic challenge. A 60-year-old Qatari lady presented with odynophagia, oral ulceration, and weight loss. Multiple physicians investigated her for over 6 months with a multitude of tests and serial gastroscopies, all of which failed to reach a conclusive diagnosis. Only after referral to a dermatologist and full body examination was diagnosis finally achieved. After reviewing the literature, we provide a summary of EBA and highlight the importance of comprehensive clinical reviews in order to avoid unnecessary morbidity.http://dx.doi.org/10.1155/2016/2839104
spellingShingle G. Kravvas
D. Veitch
C. M. Perrett
A Case of Bullous Skin Disease Presenting with Odynophagia: A Diagnostic Challenge
Case Reports in Dermatological Medicine
title A Case of Bullous Skin Disease Presenting with Odynophagia: A Diagnostic Challenge
title_full A Case of Bullous Skin Disease Presenting with Odynophagia: A Diagnostic Challenge
title_fullStr A Case of Bullous Skin Disease Presenting with Odynophagia: A Diagnostic Challenge
title_full_unstemmed A Case of Bullous Skin Disease Presenting with Odynophagia: A Diagnostic Challenge
title_short A Case of Bullous Skin Disease Presenting with Odynophagia: A Diagnostic Challenge
title_sort case of bullous skin disease presenting with odynophagia a diagnostic challenge
url http://dx.doi.org/10.1155/2016/2839104
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