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食管扁平苔藓:病例系列及文献综述

Oesophageal Lichen Planus: Case Series and Review of the Literature.

作者信息

Manzanares Nerea, Molina-Alvarez Andrea, Iglesias Mar, Naves Juan Enrique, Pujol Ramon M, Segura Sonia

机构信息

Dermatology Department, Hospital del Mar- Hospital del Mar Research Institute, Universitat Pompeu Fabra (UPF), Barcelona, Spain.

Pathology Department, Hospital del Mar- Hospital del Mar Research Institute, Universitat Pompeu Fabra (UPF), Barcelona, Spain.

出版信息

Acta Derm Venereol. 2025 Aug 11;105:adv43358. doi: 10.2340/actadv.v105.43358.

Abstract

Lichen planus affects 0.5% to 2% of the population. The involvement of the oesophagus is a rare manifestation with high morbidity and risk of malignancy. Clinical characteristics and diagnostic-therapeutic strategies were reviewed. A retrospective study of clinical-pathological characteristics, endoscopic findings, and follow-up of patients with oesophageal lichen planus treated at a tertiary hospital during 2006-2023 was conducted. Nine patients (1 man, 8 women) with a median age of 76 years were included. All patients had oral lichen planus. Dysphagia was the initial symptom, being the first manifestation of the disease in 2 cases. All presented lesions in the oral oesophagus with fibrous rings, stenosis, and mucosal denudation. Histological changes of the lichenoid type were observed in 8/9. After a median follow-up of 2 years, no progression to oesophageal squamous cell carcinoma was observed. Swallowed glucocorticoid therapy, proton pump inhibitors, prokinetics, and oesophageal dilatations were prescribed. Eight out of 9 patients showed partial improvement with clinical stabilization. Oesophageal lichen planus is an infrequent and underdiagnosed disease. Its diagnosis may be based on endoscopic features, histopathology, and direct immunofluorescence. The correct management is often challenging, but necessary because this entity has been associated with oesophageal squamous cell carcinoma.

摘要

扁平苔藓影响0.5%至2%的人群。食管受累是一种罕见表现,具有高发病率和恶性风险。对其临床特征及诊断治疗策略进行了综述。对2006年至2023年期间在一家三级医院接受治疗的食管扁平苔藓患者的临床病理特征、内镜检查结果及随访情况进行了回顾性研究。纳入9例患者(1例男性,8例女性),中位年龄76岁。所有患者均有口腔扁平苔藓。吞咽困难是初始症状,2例患者以此为疾病的首发表现。所有患者口腔食管均出现病变,表现为纤维环、狭窄及黏膜剥脱。9例中有8例观察到苔藓样组织学改变。中位随访2年后,未观察到进展为食管鳞状细胞癌。给予口服糖皮质激素治疗、质子泵抑制剂、促动力药及食管扩张治疗。9例患者中有8例临床症状部分改善并稳定。食管扁平苔藓是一种罕见且诊断不足的疾病。其诊断可基于内镜特征、组织病理学及直接免疫荧光检查。正确的治疗往往具有挑战性,但很有必要,因为该疾病与食管鳞状细胞癌有关。

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