Department of Pediatric Gastroenterology, King Abdul-Aziz Medical City, National Guard Hospital, Jeddah, Saudi Arabia.
Saudi J Gastroenterol. 2011 Mar-Apr;17(2):119-23. doi: 10.4103/1319-3767.77242.
BACKGROUND/AIM: Eosinophilic esophagitis (EE) is a clinicopathologic entity characterized by esophageal symptoms in association with a dense eosinophilic infiltrate currently defined as >15 eosinophils per high power field in the appropriate clinical context. This is the first pediatric study in Saudi Arabia to give the experience with EE and examine its symptom, histology and endoscopy results.
Retrospective chart review of all patients diagnosed with EE at National Guard Hospital, Jeddah Between 2007 and 2009. The authors identified EE on histologic criteria (≥15 eosinophils per high-power field) together with their clinical context. The authors reviewed medical records for details of clinical presentation, laboratory data, radiologic, endoscopic, and histologic findings, and the results of treatment.
We identified 15 patients in our database in the last three years. 100% of the patients were males. The median age at presentation was 10 years (range, 3-17 years). The commonly reported symptoms were failure to thrive (86%), epigastric abdominal pain (53%), poor eating (40%), dysphagia with solid food (26%), food impaction (13%), and vomiting (20%). Asthma was reported in 46% and allergic rhinitis in 40%. Peripheral eosinophilia (>0.7 Χ 10/l) was found in 66%. High serum IgE Level (>60 IU/ml) was found in 60%. Upper endoscopic analysis revealed esophageal trachealization in 46%, esophageal erythema in 46%, white specks on the esophageal mucosa in 33%, esophageal narrowing in 13%, and normal endoscopy in 13%. The mean eosinophils per high-power field was 30.4 (range, 20-71). Histologic characteristics included degranulated eosinophils (86%), basal cell hyperplasia (93%) and eosinophils clusters (micro-abscess) in 73%. The treatment of EE revealed that they used swallowed corticosteroid in 50%, proton pump inhibitors in 66%, elemental diet/ food elimination in 13% and systemic corticosteroid in 13%.
Failure to thrive and abdominal pain in a male, atopic school-aged child was the most common feature of EE. Peripheral eosinophilia, high serum IgE and endoscopic esophageal erythema and trachealization should significantly raise the clinical index of suspicion for the diagnosis of EE.
背景/目的:嗜酸性食管炎(EE)是一种临床病理实体,其特征为食管症状与密集的嗜酸性粒细胞浸润相关,目前在适当的临床背景下定义为每高倍视野 >15 个嗜酸性粒细胞。这是沙特阿拉伯首例儿科研究,提供了 EE 的经验,并检查了其症状、组织学和内镜结果。
回顾性分析 2007 年至 2009 年期间在沙特阿拉伯吉达的国民警卫队医院诊断为 EE 的所有患者的病历。作者根据组织学标准(每高倍视野≥15 个嗜酸性粒细胞)结合其临床背景确定 EE。作者查阅了病历,以了解临床表现、实验室数据、影像学、内镜和组织学发现以及治疗结果的详细信息。
在过去三年的数据库中,我们共发现了 15 名患者。100%的患者为男性。发病时的中位年龄为 10 岁(范围 3-17 岁)。常见的症状有生长发育迟缓(86%)、上腹痛(53%)、饮食不良(40%)、固体食物吞咽困难(26%)、食物嵌塞(13%)和呕吐(20%)。哮喘占 46%,过敏性鼻炎占 40%。外周血嗜酸性粒细胞计数>0.7Χ10/l 占 66%。高血清 IgE 水平(>60 IU/ml)占 60%。上消化道内镜检查显示食管气管化占 46%、食管红斑占 46%、食管黏膜上有白色斑点占 33%、食管狭窄占 13%、内镜正常占 13%。每高倍视野嗜酸性粒细胞的平均值为 30.4(范围 20-71)。组织学特征包括脱颗粒嗜酸性粒细胞(86%)、基底细胞增生(93%)和嗜酸性粒细胞簇(微脓肿)占 73%。EE 的治疗显示,50%的患者使用口服皮质类固醇,66%的患者使用质子泵抑制剂,13%的患者使用元素饮食/食物消除,13%的患者使用全身皮质类固醇。
生长发育迟缓、男性、学龄期、特应性儿童的上腹痛是 EE 的最常见特征。外周血嗜酸性粒细胞计数升高、高血清 IgE 水平和内镜下食管红斑和气管化应显著提高 EE 诊断的临床怀疑指数。