Koleva Maria, Raby Martin, Dikov Dorian
Department of General and Clinical Pathology, University Hospital St. George, Plovdiv, BGR.
Department of Pathology, Jossigny Hospital, Jossigny, FRA.
Cureus. 2024 Oct 4;16(10):e70815. doi: 10.7759/cureus.70815. eCollection 2024 Oct.
Lymphocytic esophagitis (LE) is a rare type of chronic esophagitis, marked by an increased number of peripapillary intraepithelial lymphocytes (IEL) with little to no presence of intraepithelial granulocytes and intercellular edema. There is currently no established standard for quantifying IEL in the esophageal mucosa. Clinically, LE manifests with a range of symptoms, including difficulty swallowing (dysphagia), indigestion (dyspepsia), nausea, and chest pain. It is more commonly diagnosed in older women and is often associated with tobacco use, gastroesophageal reflux disease, and achalasia, although the exact cause remains unknown. Programmed cell death protein 1 (PD-1) and its ligand (PD-L1) are expressed on the surface of immune and epithelial cells in healthy and tumor tissues, typically in response to various cytokines. We present a new case of LE associated with chronic severe psoriasis, highlighting the role of PD-L1 expression. This supports the immunopathological basis of the disease and its links to other immune and autoimmune disorders, suggesting its potential as a biomarker for distinguishing LE from reflux esophagitis.
淋巴细胞性食管炎(LE)是一种罕见的慢性食管炎,其特征是乳头周围上皮内淋巴细胞(IEL)数量增加,上皮内粒细胞几乎不存在或不存在,且细胞间水肿。目前尚无食管黏膜中IEL定量的既定标准。临床上,LE表现出一系列症状,包括吞咽困难、消化不良、恶心和胸痛。它在老年女性中更常见,并且通常与吸烟、胃食管反流病和贲门失弛缓症有关,尽管确切病因尚不清楚。程序性细胞死亡蛋白1(PD-1)及其配体(PD-L1)在健康组织和肿瘤组织的免疫细胞和上皮细胞表面表达,通常是对各种细胞因子的反应。我们报告了一例与慢性重度银屑病相关的LE新病例,突出了PD-L1表达的作用。这支持了该疾病的免疫病理学基础及其与其他免疫和自身免疫性疾病的联系,表明其作为区分LE与反流性食管炎生物标志物的潜力。