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Histopathologic variability and endoscopic correlates in adults with eosinophilic esophagitis - 16/08/11

Doi : 10.1016/j.gie.2006.04.037 
Nirmala Gonsalves, MD, Maria Policarpio-Nicolas, MD, Qing Zhang, MD, M. Sambasiva Rao, MD, Ikuo Hirano, MD
Current affiliations: Division of Gastroenterology (Drs Gonsalves, Zhang, and Hirano), Division of Pathology (Drs Policarpio-Nicolas and Rao), Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA 

Reprint requests: Ikuo Hirano, MD, Division of Gastroenterology and Hepatology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611-2951.

Chicago, Illinois, USA

Abstract

Background

Recently recognized as an important cause of dysphagia and food impaction in adults, eosinophilic esophagitis (EE) is diagnosed by histologic findings of increased mucosal eosinophils.

Objective

We examined variability in histopathologic features of adults with EE to derive a recommendation on the optimal number and location of biopsies needed for diagnosis.

Design

Charts were reviewed from 74 patients diagnosed with EE based on ≥15 eosinophils per high-power field (eos/hpf). Biopsy specimens were prospectively analyzed for the degree of eosinophilia and histopathologic features of EE. Subgroup analysis was performed in patients with biopsy specimens from both the proximal and the distal esophagus. The biopsy specimens from patients with EE were compared with specimens from biopsied Schatzki’s ring.

Setting

Northwestern University Feinberg School of Medicine.

Patients

Charts were reviewed for 74 adult patients and biopsy specimens were available for 66 patients.

Results

A total of 341 biopsy specimens from 66 patients were available for analysis and revealed marked variability within and between biopsy specimens of individual patients. The median eos/hpf was 107 (0-557 eos/hpf). By using criteria of ≥15 eos/hpf for diagnosis, we found that 1 biopsy specimen had a sensitivity of 55%, which increased to 100% after 5 biopsies. By using stricter criteria, additional biopsy specimens were needed to achieve 100% sensitivity. Despite a higher eosinophilia in distal (82 eos/hpf) compared with proximal biopsy specimens (68 eos/hpf), this difference was not statistically significant. There was marked difference between eosinophilia in mucosal biopsy specimens of patients with EE (82 eos/hpf) compared with Schatzki’s ring (0.3 eos/hpf).

Conclusions

Significant histologic variability exists among biopsy specimens from individual patients with EE and necessitates multiple biopsies to improve diagnostic sensitivity. No significant difference in eosinophilia was demonstrated between proximal and distal sites.

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© 2006  American Society for Gastrointestinal Endoscopy. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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Vol 64 - N° 3

P. 313-319 - settembre 2006 Ritorno al numero
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