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Esophageal lichen planus: Current knowledge, challenges and future perspectives. | LitMetric

Esophageal lichen planus: Current knowledge, challenges and future perspectives.

World J Gastroenterol

Department of Medicine II, Gastroenterology, Hepatology, Endocrinology and Infectious Diseases, Medical Center-University of Freiburg, Faculty of Medicine, Freiburg 79106, Germany.

Published: November 2022

AI Article Synopsis

  • Lichen planus (LP) is a chronic inflammatory disease that can affect the skin and mucous membranes, with esophageal involvement (ELP) being notable but often underdiagnosed.
  • The primary symptom of ELP is dysphagia (difficulty swallowing), especially in middle-aged women, and it can present asymptomatically despite the presence of significant lesions.
  • There is no definitive treatment for ELP, but topical steroids can improve symptoms for many patients; chronic cases might require more aggressive therapies and could pose a risk for esophageal cancer.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669830PMC
http://dx.doi.org/10.3748/wjg.v28.i41.5893DOI Listing

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