Clinicopathologic Analysis of Proton Pump Inhibitor-Responsive Esophageal Eosinophilia in Korean Patients.
- Author:
Da Hyun JUNG
1
;
Gak Won YUN
;
Yoo Jin LEE
;
Yunju JO
;
Hyojin PARK
Author Information
- Publication Type:Original Article
- Keywords: Proton pump inhibitor responsive esophageal eosinophilia; Eosinophilic esophagitis; Proton pump inhibitors
- MeSH: Adult; Asian Continental Ancestry Group; Chest Pain/etiology; Deglutition Disorders/etiology; Diagnosis, Differential; Eosinophilic Esophagitis/complications/*drug therapy/*pathology; Esophagus/pathology; Female; Follow-Up Studies; Gastroesophageal Reflux/etiology; Heartburn/etiology; Humans; Male; Middle Aged; Pharyngitis/etiology; Phenotype; Proton Pump Inhibitors/*therapeutic use; Republic of Korea; Retrospective Studies; Sensation Disorders/etiology; Treatment Outcome; Young Adult
- From:Gut and Liver 2016;10(1):37-41
- CountryRepublic of Korea
- Language:English
- Abstract: BACKGROUND/AIMS: Proton pump inhibitor-responsive esophageal eosinophilia (PPI-REE) is a newly recognized form of eosinophilic esophagitis (EoE) that responds to PPI therapy. It remains unclear whether PPI-REE represents a subphenotype of gastroesophageal reflux disease, a subphenotype of EoE, or its own distinct entity. The aim was to evaluate the clinicopathologic features of PPI-REE. METHODS: Six patients were diagnosed with PPI-REE based on symptoms, endoscopic abnormalities, esophageal eosinophilia with > or =15 eosinophils/high-power field, and a response to PPI treatment. Symptoms and endoscopic and pathological findings were evaluated. RESULTS: The median follow-up duration was 12 months. Presenting symptoms included dysphagia, heartburn, chest pain, foreign body sensation, acid reflux, and sore throat. All patients had typical endoscopic findings of EoE such as esophageal rings, linear furrows, nodularity, and whitish plaques. Three patients had a concomitant allergic disorder, and one had reflux esophagitis. Four patients exhibited elevated serum IgE, and five had positive skin prick tests. All patients experienced symptomatic resolution within 4 weeks and histologic resolution within 8 weeks after starting PPI therapy. There was no symptomatic recurrence. CONCLUSIONS: PPI therapy induced rapid resolution of symptoms and eosinophil counts in patients with PPI-REE. Large-scale studies with long-term follow-up are warranted.
