Sunkara Tagore, Rawla Prashanth, Yarlagadda Krishna Sowjanya, Gaduputi Vinaya
Division of Gastroenterology and Hepatology, Mercy Medical Center, Des Moines, IA 50314, USA.
Division of Gastroenterology, St. Barnabas Hospital Health System, New York, NY, 10457, USA.
Clin Exp Gastroenterol. 2019 Jun 5;12:239-253. doi: 10.2147/CEG.S173130. eCollection 2019.
Eosinophilic gastroenteritis (EGE) is a digestive disorder in children and adults that is characterized by eosinophilic infiltration in the stomach and intestine. The underlying molecular mechanisms predisposing to this disease are unknown, but it seems that hypersensitivity response plays a major role in its pathogenesis, as many patients have a history of seasonal allergies, food sensitivities, asthma, and eczema. Symptoms and clinical presentations vary, depending on the site and layer of the gastrointestinal wall infiltrated by eosinophils. Laboratory results, radiological findings, and endoscopy can provide important diagnostic evidence for EGE; however, the cornerstone of the diagnosis remains the histological examination of gastric and duodenal specimens for evidence of eosinophilic infiltration (>20 eosinophils per high-power field), and finally clinicians make the diagnosis in correlation with and by exclusion of other disorders associated with eosinophilic infiltration. Although spontaneous remission is reported in around 30%-40% of EGE cases, most patients require ongoing treatment. The management options for this disorder include both dietary and pharmacological approaches, with corticosteroids being the mainstay of therapy and highly effective. The subsequent course is quite variable. Some patients have no recurrences, while a few experience recurrent symptoms during or immediately after corticosteroid interruption. An alternative therapeutic armamentarium includes mast-cell stabilizers, leukotriene antagonists, antihistamines, immunomodulators, and biological agents. In this review, we provide a summary of the different diagnostic tools utilized in practice, as well as the different therapeutic approaches available for EGE management.
嗜酸性粒细胞性胃肠炎(EGE)是一种发生于儿童和成人的消化系统疾病,其特征是胃和肠道出现嗜酸性粒细胞浸润。导致这种疾病的潜在分子机制尚不清楚,但超敏反应似乎在其发病机制中起主要作用,因为许多患者有季节性过敏、食物过敏、哮喘和湿疹病史。症状和临床表现各不相同,这取决于嗜酸性粒细胞浸润的胃肠道壁的部位和层次。实验室检查结果、影像学检查结果和内镜检查可为EGE提供重要的诊断依据;然而,诊断的关键仍然是对胃和十二指肠标本进行组织学检查,以寻找嗜酸性粒细胞浸润的证据(每高倍视野>20个嗜酸性粒细胞),最后临床医生通过与其他伴有嗜酸性粒细胞浸润的疾病进行关联和排除来做出诊断。虽然约30%-40%的EGE病例报告有自发缓解,但大多数患者需要持续治疗。这种疾病的治疗选择包括饮食和药物治疗方法,其中皮质类固醇是主要的治疗手段且疗效显著。后续病程差异很大。一些患者没有复发,而少数患者在皮质类固醇中断期间或之后立即出现复发症状。其他治疗手段包括肥大细胞稳定剂、白三烯拮抗剂、抗组胺药、免疫调节剂和生物制剂。在本综述中,我们总结了实践中使用的不同诊断工具以及EGE管理可用的不同治疗方法。