Khan Seema, Orenstein Susan R, Di Lorenzo Carlo, Kocoshis Samuel A, Putnam Philip E, Sigurdsson Luther, Shalaby Theresa M
Division of Pediatric Gastroenterology, University of Pittsburgh School of Medicine, Children's Hospital of Pittsburgh, 3705 Fifth Avenue, Pittsburgh, Pennsylvania 15213-2583, USA.
Dig Dis Sci. 2003 Jan;48(1):22-9. doi: 10.1023/a:1021769928180.
Eosinophilic esophagitis, long known to be a feature of acid reflux, has recently been described in patients with food allergies and macroscopically furrowed esophagus. The pathophysiology and optimal management of patients with eosinophilic esophagitis is unclear. We describe our clinical experience related to eosinophilic esophagitis and obstructive symptoms in children and propose etiopathogenesis and management guidelines. Twelve children with obstructive esophageal symptoms (11 male), median age 5 years, and identified to have eosinophilic esophagitis with > 5 eosinophils per high-power field (eos/hpf) are reported. Of these, four had strictures, six had impactions, and two had only dysphagia. A diagnostic evaluation included esophagogastroduodenoscopy with biopsies in all and upper gastrointestinal series, IgE, radioallergosorbent tests, and skin tests for food allergies in some cases. Esophageal histology specimens were independently analyzed for eosinophil density by two authors. Four of five children with > 20 eos/hpf responded to elimination diets/steroids. The fifth child responded to a fundoplication. Seven children had 5-20 eos/hpf and three of them with no known food allergies responded to antireflux therapy alone. Three others in this group with positive food allergies responded to treatment with elimination diets and/or steroids. The seventh patient in this group was lost to follow-up. In conclusion, on the basis of response to therapy, eosinophilic esophagitis can be subdivided into two groups: those with likely gastroesophageal reflux disease if < 20 eos/hpf and no food allergies, and others with allergic eosinophilic esophagitis associated with food allergies and often with > 20 eos/hpf.
嗜酸性食管炎长期以来被认为是胃酸反流的一个特征,最近在食物过敏和食管出现肉眼可见皱襞的患者中也有描述。嗜酸性食管炎患者的病理生理学和最佳治疗方法尚不清楚。我们描述了与儿童嗜酸性食管炎和梗阻症状相关的临床经验,并提出了病因发病机制和治疗指南。报告了12例有食管梗阻症状的儿童(11例男性),中位年龄5岁,经鉴定患有嗜酸性食管炎,每高倍视野(eos/hpf)嗜酸性粒细胞>5个。其中,4例有狭窄,6例有食物嵌塞,2例仅有吞咽困难。诊断评估包括对所有患者进行食管胃十二指肠镜检查及活检,部分患者进行上消化道造影、IgE、放射变应原吸附试验和食物过敏皮肤试验。两位作者独立分析食管组织学标本的嗜酸性粒细胞密度。5例每高倍视野嗜酸性粒细胞>20个的儿童中有4例对饮食排除/类固醇治疗有反应。第5例儿童对胃底折叠术有反应。7例儿童每高倍视野嗜酸性粒细胞为5 - 20个,其中3例无已知食物过敏,仅对抗反流治疗有反应。该组另外3例食物过敏检测呈阳性的儿童对饮食排除和/或类固醇治疗有反应。该组第7例患者失访。总之,根据治疗反应,嗜酸性食管炎可分为两组:每高倍视野嗜酸性粒细胞<20个且无食物过敏的患者可能患有胃食管反流病,其他患者患有与食物过敏相关的过敏性嗜酸性食管炎,通常每高倍视野嗜酸性粒细胞>20个。