Gastrointestinal Endoscopy
Volume 61, Issue 7 , Pages 795-801, June 2005

Association of eosinophilic inflammation with esophageal food impaction in adults

Current affiliations: Department of Medicine, Department of Pathology, Beaumont Hospital, Royal Oak, Michigan; Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts; Combined Program in Pediatric Gastroenterology and Nutrition, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts, USA

Received 28 September 2004; accepted 31 January 2005.

Royal Oak, Michigan, USA

Introduction

Esophageal food impaction is a common presentation of eosinophilic esophagitis. The prevalence of eosinophilic esophagitis among patients with food impaction is unknown. To address this, we evaluated clinicopathologic features of adults with food impaction.

Methods

For a 3-year period, patients from a single, adult, community-based gastroenterology practice with esophageal food impaction were evaluated. Histories were assessed and esophageal biopsy specimens were evaluated by routine and immunohistochemical techniques.

Results

Thirty-one patients with food impaction were evaluated. Seventeen of 31 patients had >20 eosinophils/high power field (HPF) without gender predilection. Thirteen of these 17 patients had been treated with proton pump inhibitors at the time biopsy specimens were obtained. Patients with >20 eosinophils/HPF were significantly younger (mean age 42 ± 4 years) than patients with <20 eosinophils/HPF (mean age 70+3 years). Superficial white exudates and eosinophilic microabscesses in the squamous epithelium were features observed only in patients with >20 eosinophils/HPF. Immunopathologic analysis demonstrated increased CD8 lymphocytes and major basic protein deposition in their squamous epithelium.

Conclusions

More than half of patients with esophageal food impaction in a primary gastroenterology practice have >20 eosinophils/HPF. Based on clinicopathologic features, a significant number likely have eosinophilic esophagitis.

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 See CME section; p. 872.Supported by National Institutes of Health grant DK062245.This work was presented, in part, at Digestive Diseases Week, May 19-23, 2002, San Francisco, California.

PII: S0016-5107(05)00313-5

Gastrointestinal Endoscopy
Volume 61, Issue 7 , Pages 795-801, June 2005