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Esophageal lichen planus: Current knowledge, challenges and future perspectives
Lichen planus (LP) is a frequent, chronic inflammatory disease involving the skin, mucous membranes and/or skin appendages. Esophageal involvement in lichen planus (ELP) is a clinically important albeit underdiagnosed inflammatory condition. This narrative review aims to give an overview of the curr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669830/ https://www.ncbi.nlm.nih.gov/pubmed/36405107 http://dx.doi.org/10.3748/wjg.v28.i41.5893 |
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author | Decker, Annegrit Schauer, Franziska Lazaro, Adhara Monasterio, Carmen Schmidt, Arthur Robert Schmitt-Graeff, Annette Kreisel, Wolfgang |
author_facet | Decker, Annegrit Schauer, Franziska Lazaro, Adhara Monasterio, Carmen Schmidt, Arthur Robert Schmitt-Graeff, Annette Kreisel, Wolfgang |
author_sort | Decker, Annegrit |
collection | PubMed |
description | Lichen planus (LP) is a frequent, chronic inflammatory disease involving the skin, mucous membranes and/or skin appendages. Esophageal involvement in lichen planus (ELP) is a clinically important albeit underdiagnosed inflammatory condition. This narrative review aims to give an overview of the current knowledge on ELP, its prevalence, pathogenesis, clinical manifestation, diagnostic criteria, and therapeutic options in order to provide support in clinical management. Studies on ELP were collected using PubMed/Medline. Relevant clinical and therapeutical characteristics from published patient cohorts including our own cohort were extracted and summarized. ELP mainly affects middle-aged women. The principal symptom is dysphagia. However, asymptomatic cases despite progressed macroscopic esophageal lesions may occur. The pathogenesis is unknown, however an immune-mediated mechanism is probable. Endoscopically, ELP is characterized by mucosal denudation and tearing, trachealization, and hyperkeratosis. Scarring esophageal stenosis may occur in chronic courses. Histologic findings include mucosal detachment, T-lymphocytic infiltrations, epithelial apoptosis (Civatte bodies), dyskeratosis, and hyperkeratosis. Direct immuno-fluorescence shows fibrinogen deposits along the basement membrane zone. To date, there is no established therapy. However, treatment with topical steroids induces symptomatic and histologic improvement in two thirds of ELP patients in general. More severe cases may require therapy with immunosuppressors. In symptomatic esophageal stenosis, endoscopic dilation may be necessary. ELP may be regarded as a precancerous condition as transition to squamous cell carcinoma has been documented in literature. ELP is an underdiagnosed yet clinically important differential diagnosis for patients with unclear dysphagia or esophagitis. Timely diagnosis and therapy might prevent potential sequelae such as esophageal stenosis or development of invasive squamous cell carcinoma. Further studies are needed to gain more knowledge about the pathogenesis and treatment options. |
format | Online Article Text |
id | pubmed-9669830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-96698302022-11-18 Esophageal lichen planus: Current knowledge, challenges and future perspectives Decker, Annegrit Schauer, Franziska Lazaro, Adhara Monasterio, Carmen Schmidt, Arthur Robert Schmitt-Graeff, Annette Kreisel, Wolfgang World J Gastroenterol Review Lichen planus (LP) is a frequent, chronic inflammatory disease involving the skin, mucous membranes and/or skin appendages. Esophageal involvement in lichen planus (ELP) is a clinically important albeit underdiagnosed inflammatory condition. This narrative review aims to give an overview of the current knowledge on ELP, its prevalence, pathogenesis, clinical manifestation, diagnostic criteria, and therapeutic options in order to provide support in clinical management. Studies on ELP were collected using PubMed/Medline. Relevant clinical and therapeutical characteristics from published patient cohorts including our own cohort were extracted and summarized. ELP mainly affects middle-aged women. The principal symptom is dysphagia. However, asymptomatic cases despite progressed macroscopic esophageal lesions may occur. The pathogenesis is unknown, however an immune-mediated mechanism is probable. Endoscopically, ELP is characterized by mucosal denudation and tearing, trachealization, and hyperkeratosis. Scarring esophageal stenosis may occur in chronic courses. Histologic findings include mucosal detachment, T-lymphocytic infiltrations, epithelial apoptosis (Civatte bodies), dyskeratosis, and hyperkeratosis. Direct immuno-fluorescence shows fibrinogen deposits along the basement membrane zone. To date, there is no established therapy. However, treatment with topical steroids induces symptomatic and histologic improvement in two thirds of ELP patients in general. More severe cases may require therapy with immunosuppressors. In symptomatic esophageal stenosis, endoscopic dilation may be necessary. ELP may be regarded as a precancerous condition as transition to squamous cell carcinoma has been documented in literature. ELP is an underdiagnosed yet clinically important differential diagnosis for patients with unclear dysphagia or esophagitis. Timely diagnosis and therapy might prevent potential sequelae such as esophageal stenosis or development of invasive squamous cell carcinoma. Further studies are needed to gain more knowledge about the pathogenesis and treatment options. Baishideng Publishing Group Inc 2022-11-07 2022-11-07 /pmc/articles/PMC9669830/ /pubmed/36405107 http://dx.doi.org/10.3748/wjg.v28.i41.5893 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Review Decker, Annegrit Schauer, Franziska Lazaro, Adhara Monasterio, Carmen Schmidt, Arthur Robert Schmitt-Graeff, Annette Kreisel, Wolfgang Esophageal lichen planus: Current knowledge, challenges and future perspectives |
title | Esophageal lichen planus: Current knowledge, challenges and future perspectives |
title_full | Esophageal lichen planus: Current knowledge, challenges and future perspectives |
title_fullStr | Esophageal lichen planus: Current knowledge, challenges and future perspectives |
title_full_unstemmed | Esophageal lichen planus: Current knowledge, challenges and future perspectives |
title_short | Esophageal lichen planus: Current knowledge, challenges and future perspectives |
title_sort | esophageal lichen planus: current knowledge, challenges and future perspectives |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669830/ https://www.ncbi.nlm.nih.gov/pubmed/36405107 http://dx.doi.org/10.3748/wjg.v28.i41.5893 |
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