Cargando…

Retrospective analysis of autoimmune bullous diseases in Middle Franconia

INTRODUCTION: Autoimmune bullous diseases (AIBDs) are a group of rare cutaneous disorders affecting cornified skin and mucous membranes. They are characterized by tense or flaccid blistering and erosions due to autoantibodies against desmosomal and hemidesmosomal structural proteins of the skin. Thi...

Descripción completa

Detalles Bibliográficos
Autores principales: Sollfrank, Lukas, Schönfelder, Valerie, Sticherling, Micheal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10595001/
https://www.ncbi.nlm.nih.gov/pubmed/37881435
http://dx.doi.org/10.3389/fimmu.2023.1256617
_version_ 1785124770592849920
author Sollfrank, Lukas
Schönfelder, Valerie
Sticherling, Micheal
author_facet Sollfrank, Lukas
Schönfelder, Valerie
Sticherling, Micheal
author_sort Sollfrank, Lukas
collection PubMed
description INTRODUCTION: Autoimmune bullous diseases (AIBDs) are a group of rare cutaneous disorders affecting cornified skin and mucous membranes. They are characterized by tense or flaccid blistering and erosions due to autoantibodies against desmosomal and hemidesmosomal structural proteins of the skin. This group of disorders can be divided into those of pemphigoid and those of pemphigus diseases. If left untreated, these autoimmune diseases can cause serious or even life-threatening complications such as loss of fluid, superinfections or impaired food intake. Due to modern standardized serological assays, the diagnosis of AIBDs can usually be confirmed in combination with their clinical appearance. Whereas for a long time corticosteroids were the major players in the treatment of these diseases, with the approval of rituximab and other immunosuppressive agents, the therapy has increasingly improved. METHODS: In this study, we aimed to investigate epidemiologic and clinical features as well as diagnostics and therapy of bullous autoimmune diseases in Middle Franconia, a governorate within the German federal state of Bavaria. Patients diagnosed or treated because of a AIBDs between 01.04.2013 and 31.03.2019 at the dermatological department of the university hospital Erlangen were included in this retrospective study (n = 242). Patients were either diagnosed for the first time (n=176) or the diagnosis has been confirmed (n=66) at the department. The respective incidence was calculated among the 176 subjects who had been diagnosed at the center in this period. Data was taken from patient records and analyzed with Microsoft® Excel. The evaluation included the diagnoses of pemphigus vulgaris (PV), pemphigus foliaceus (PF), bullous pemphigoid (BP), mucous membrane pemphigoid (MMP), linear IgA dermatosis (LAD), epidermolysis bullosa acquisita (EBA), and dermatitis herpetiformis (DH). RESULTS: This study shows that the incidence of each AIBDs in Middle Franconia is low and comparable (PV, PF, LAD, EBA) or lower (BP, MMP, DH) than in other studies and regions. BP is the most common newly diagnosed AIBD in Middle Franconia. DISCUSSION: Due to the chronic and sometimes severe course of AIBDs, repeated in-house treatments are often necessary. To date, mainly topically and systemically applied corticosteroids in combination with immunomodulators are used as first-line therapy.
format Online
Article
Text
id pubmed-10595001
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-105950012023-10-25 Retrospective analysis of autoimmune bullous diseases in Middle Franconia Sollfrank, Lukas Schönfelder, Valerie Sticherling, Micheal Front Immunol Immunology INTRODUCTION: Autoimmune bullous diseases (AIBDs) are a group of rare cutaneous disorders affecting cornified skin and mucous membranes. They are characterized by tense or flaccid blistering and erosions due to autoantibodies against desmosomal and hemidesmosomal structural proteins of the skin. This group of disorders can be divided into those of pemphigoid and those of pemphigus diseases. If left untreated, these autoimmune diseases can cause serious or even life-threatening complications such as loss of fluid, superinfections or impaired food intake. Due to modern standardized serological assays, the diagnosis of AIBDs can usually be confirmed in combination with their clinical appearance. Whereas for a long time corticosteroids were the major players in the treatment of these diseases, with the approval of rituximab and other immunosuppressive agents, the therapy has increasingly improved. METHODS: In this study, we aimed to investigate epidemiologic and clinical features as well as diagnostics and therapy of bullous autoimmune diseases in Middle Franconia, a governorate within the German federal state of Bavaria. Patients diagnosed or treated because of a AIBDs between 01.04.2013 and 31.03.2019 at the dermatological department of the university hospital Erlangen were included in this retrospective study (n = 242). Patients were either diagnosed for the first time (n=176) or the diagnosis has been confirmed (n=66) at the department. The respective incidence was calculated among the 176 subjects who had been diagnosed at the center in this period. Data was taken from patient records and analyzed with Microsoft® Excel. The evaluation included the diagnoses of pemphigus vulgaris (PV), pemphigus foliaceus (PF), bullous pemphigoid (BP), mucous membrane pemphigoid (MMP), linear IgA dermatosis (LAD), epidermolysis bullosa acquisita (EBA), and dermatitis herpetiformis (DH). RESULTS: This study shows that the incidence of each AIBDs in Middle Franconia is low and comparable (PV, PF, LAD, EBA) or lower (BP, MMP, DH) than in other studies and regions. BP is the most common newly diagnosed AIBD in Middle Franconia. DISCUSSION: Due to the chronic and sometimes severe course of AIBDs, repeated in-house treatments are often necessary. To date, mainly topically and systemically applied corticosteroids in combination with immunomodulators are used as first-line therapy. Frontiers Media S.A. 2023-10-10 /pmc/articles/PMC10595001/ /pubmed/37881435 http://dx.doi.org/10.3389/fimmu.2023.1256617 Text en Copyright © 2023 Sollfrank, Schönfelder and Sticherling https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Sollfrank, Lukas
Schönfelder, Valerie
Sticherling, Micheal
Retrospective analysis of autoimmune bullous diseases in Middle Franconia
title Retrospective analysis of autoimmune bullous diseases in Middle Franconia
title_full Retrospective analysis of autoimmune bullous diseases in Middle Franconia
title_fullStr Retrospective analysis of autoimmune bullous diseases in Middle Franconia
title_full_unstemmed Retrospective analysis of autoimmune bullous diseases in Middle Franconia
title_short Retrospective analysis of autoimmune bullous diseases in Middle Franconia
title_sort retrospective analysis of autoimmune bullous diseases in middle franconia
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10595001/
https://www.ncbi.nlm.nih.gov/pubmed/37881435
http://dx.doi.org/10.3389/fimmu.2023.1256617
work_keys_str_mv AT sollfranklukas retrospectiveanalysisofautoimmunebullousdiseasesinmiddlefranconia
AT schonfeldervalerie retrospectiveanalysisofautoimmunebullousdiseasesinmiddlefranconia
AT sticherlingmicheal retrospectiveanalysisofautoimmunebullousdiseasesinmiddlefranconia