Volume 119, Issue 3 , Pages 731-738, March 2007
Pediatric patients with eosinophilic esophagitis: An 8-year follow-up
Background
Eosinophilic esophagitis (EE) is a gastrointestinal disorder that is increasingly diagnosed in pediatric patients.
Objective
We aimed to define, in pediatric patients with EE, their demographic and atopic characteristics, the histopathology of all segments of the gastrointestinal tract, and the effect of therapeutic interventions on the natural history.
Methods
We conducted a retrospective analysis of a database of pediatric patients with EE followed over a period of 8 years.
Results
In 89 pediatric patients with EE, male sex (78.6%), white race (94.4%), young age at diagnosis, mean ± SD, 6.2 ± 4.8 years, and atopy with sensitization to environmental and food allergens in 79% and 75%, respectively, were prevalent. Patients had EE of the proximal and distal esophagus, and 77% had in addition either mucosal eosinophilia or noneosinophilic histopathology in the stomach, duodenum, and colon. EE was chronic, with a duration of mean ± SD, 0.91 ± 0.84 years, until first resolution, and was recurrent; of 66% of the patients who had resolution, 79% later relapsed.
Conclusion
Eosinophilic esophagitis in the pediatric population is a chronic and relapsing condition, associated with atopy and sometimes with subsequent histopathology in segments of the gastrointestinal tract other than the esophagus.
Clinical implications
Physicians evaluating pediatric patients with chronic gastrointestinal symptoms should consider the diagnosis of EE, particularly in young white male patients with atopy. Once diagnosed and treated, the physicians should follow the patients over a period of several years because the course of the disease is protracted, other gastrointestinal segments may be affected, and relapses are common.
Key words: Eosinophilic esophagitis, food allergy, atopy patch test, eosinophil, pediatric, eosinophilic gastroenteritis, environmental allergy, atopy, skin test
Abbreviations used: EE, Eosinophilic esophagitis, Hpf, High-power field, SPT, Skin prick test
Supported by a 2005 American Academy of Allergy, Asthma & Immunology/Sanofi Aventis Women Physicians in Allergy Project Grant Award (A.H.A.) and a 2004 American Academy of Allergy, Asthma & Immunology Clinical Fellowship Award (J.Z.B.).Disclosure of potential conflict of interest: A. H. Assa'ad has consulting arrangements with and has received grant support from GlaxoSmithKline. M. H. Collins has consulting arrangements with GlaxoSmithKline and Ception Therapeutics. R. J. Noel has consulting arrangements with Ception Therapeutics. M. E. Rothenberg has consulting arrangements with GlaxoSmithKline, Ception Therapeutics, Cambridge Antibody Technology, Tanox, and MedaCorp; owns stock in Ception Therapeutics; has received grant support from Cambridge Antibody Technology; and is on the speakers' bureau for Merck. The rest of the authors have declared that they have no conflict of interest.
PII: S0091-6749(06)03792-4
doi:10.1016/j.jaci.2006.10.044
© 2007 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
Volume 119, Issue 3 , Pages 731-738, March 2007
