Esophageal lichen planus: Current knowledge, challenges and future perspectives

被引:11
|
作者
Decker, Annegrit [1 ]
Schauer, Franziska [2 ]
Lazaro, Adhara [3 ]
Monasterio, Carmen [1 ]
Schmidt, Arthur Robert [1 ]
Schmitt-Graeff, Annette [4 ,5 ]
Kreisel, Wolfgang [1 ,6 ]
机构
[1] Univ Freiburg, Fac Med, Med Ctr, Dept Med 2,Gastroenterol Hepatol Endocrinol & Infe, D-79106 Freiburg, Germany
[2] Univ Freiburg, Fac Med, Med Ctr, Dept Dermatol, D-79104 Freiburg, Germany
[3] Univ Freiburg, Dept Med, Inst Exercise & Occupat Med, Fac Med,Med Ctr, D-79106 Freiburg, Germany
[4] Inst Dermatohistol Pathol & Mol Pathol Prof Dr Laa, Freiburg, Germany
[5] Univ Freiburg, D-79106 Freiburg, Germany
[6] Univ Freiburg, Fac Med, Med Ctr, Dept Med 2,Gastroenterol Hepatol Endocrinol & Infe, Hugstetter Str 55, D-79106 Freiburg, Germany
关键词
Lichen planus; Esophagitis; T-lymphocytes; Budesonide; Dysphagia; Precancerosis; MALIGNANT-TRANSFORMATION; EOSINOPHILIC ESOPHAGITIS; EPIDERMOID METAPLASIA; LYMPHOCYTIC ESOPHAGITIS; DISSECANS SUPERFICIALIS; INVOLVEMENT; MANAGEMENT; DISEASE; RISK; ASSOCIATION;
D O I
10.3748/wjg.v28.i41.5893
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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.
引用
收藏
页码:5893 / 5909
页数:17
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