Centre for Digestive Motility, Division of Gastroenterology, Department of Medicine, University of Calgary Faculty of Medicine, Calgary, AB, Canada.
Gut Liver. 2013 Jul;7(4):401-5. doi: 10.5009/gnl.2013.7.4.401. Epub 2013 Jun 11.
BACKGROUND/AIMS: Esophageal lichen planus (LP) has been described as a cause of nonspecific esophagitis that may cause dysphagia, but its incidence is unknown. We aimed to estimate the incidence of esophageal LP in a defined geographic region and describe the clinical characteristics of affected patients.
A histopathology database for a population of 1 million people was searched for all esophageal mucosal biopsy results over an 8-year period. Cases showing inflammation or abnormalities without a diagnosis after three or more biopsies were reviewed for findings of LP.
Of 13,589 esophageal biopsies, only one received a diagnosis of LP. Seven patients (four male; mean age, 59 years; range, 39 to 76 years) were identified as having chronic dysphagia and nonspecific proximal esophagitis for which no diagnosis could be made. All patients had proximal inflammation, and six of seven had full-thickness lymphocytic infiltration. Elongation of the lamina propria papillae was noted in all patients, whereas six patients had parakeratosis and ballooning. Only one patient had findings potentially consistent with, but not sufficient for, a diagnosis of esophageal LP.
Esophageal LP appears to be extremely uncommon in this North American population, and esophageal biopsy alone is likely not sufficient to establish a diagnosis of LP.
背景/目的:食管扁平苔藓(LP)被描述为一种非特异性食管炎的病因,可能导致吞咽困难,但其发病率尚不清楚。我们旨在估计特定地理区域内食管 LP 的发病率,并描述受影响患者的临床特征。
对 100 万人的组织病理学数据库进行了为期 8 年的食管黏膜活检结果搜索。对经过三次以上活检仍未诊断的炎症或异常病例进行了回顾,以寻找 LP 的发现。
在 13589 例食管活检中,仅一例被诊断为 LP。7 名患者(4 名男性;平均年龄 59 岁;范围 39 至 76 岁)出现慢性吞咽困难和非特异性近端食管炎,无法做出诊断。所有患者均有近端炎症,7 例中有 6 例有全层淋巴细胞浸润。所有患者的固有膜乳头均有伸长,而 6 例有角化过度和气球样变。仅有 1 例患者的发现可能符合但不足以诊断为食管 LP。
在这个北美人种中,食管 LP 似乎极为罕见,单独进行食管活检可能不足以确立 LP 的诊断。