Volume 68, Issue 5 pp. 689-694
Original Article: Gastroenterology: Eosinophilic Gastrointestinal Diseases

Esophageal IgG4

Clinical, Endoscopic, and Histologic Correlations in Eosinophilic Esophagitis

Amanda E. Pope

Amanda E. Pope

Division of Pediatric Gastroenterology, Hepatology and Nutrition, Los Angeles, CA

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Nicholas Stanzione

Nicholas Stanzione

Pathology and Laboratory Medicine, Los Angeles, CA

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Bita V. Naini

Bita V. Naini

Pathology and Laboratory Medicine, Los Angeles, CA

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Maria Garcia-Lloret

Maria Garcia-Lloret

Allergy and Immunology, Los Angeles, CA

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Kevin A. Ghassemi

Kevin A. Ghassemi

Gastroenterology, UCLA, Los Angeles, CA

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Elizabeth A. Marcus

Elizabeth A. Marcus

Division of Pediatric Gastroenterology, Hepatology and Nutrition, Los Angeles, CA

VA Greater Los Angeles Health System, Los Angeles, CA

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Martin G. Martin

Martin G. Martin

Division of Pediatric Gastroenterology, Hepatology and Nutrition, Los Angeles, CA

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Laura J. Wozniak

Corresponding Author

Laura J. Wozniak

Division of Pediatric Gastroenterology, Hepatology and Nutrition, Los Angeles, CA

Address correspondence and reprint requests to Laura J. Wozniak, MD, MS, Department of Pediatrics, Division of Pediatric Gastroenterology, Hepatology and Nutrition, University of California Los Angeles, 10833 Le Conte Ave, MDCC 12-383, Los Angeles, CA 90095 (e-mail: [email protected]).Search for more papers by this author
First published: 01 May 2019
Citations: 20

Supplemental digital content is available for this article. Direct URL citations appear in the printed text, and links to the digital files are provided in the HTML text of this article on the journal's Web site (www.jpgn.org).

The authors report no conflicts of interest.

ABSTRACT

Objective:

Recent studies show increased serum and esophageal IgG4 in patients with eosinophilic esophagitis (EoE), suggesting a possible IgG4-involved process. The role of IgG4 in pediatric EoE has not been extensively investigated. Our aim was to analyze IgG4 in esophageal tissue in children in parallel to that in adults with EoE.

Methods:

In a retrospective institutional review board–approved study, we performed immunohistochemical staining of IgG4 in esophageal biopsy specimens from 39 subjects: children with EoE (n = 16), adults with EoE (n = 15), children with reflux esophagitis (n = 4), and pediatric controls (n = 4). We assessed the relationships between IgG4 staining and clinical, endoscopic, and histopathologic characteristics.

Results:

Patients with EoE were significantly more likely to stain positively for IgG4 than children with reflux esophagitis or controls (P = 0.015). Fifteen of 31 (48%) EoE cases stained positively for IgG4. None of the reflux esophagitis or control cases stained positively. IgG4 staining had 48% sensitivity and 100% specificity for EoE. There was a trend toward IgG4 staining being associated with foreign body/food impaction (P = 0.153). There was a strong association between distal IgG4 staining and basal zone hyperplasia (P = 0.003).

Conclusions:

Our study suggests IgG4 is not a consistent finding of EoE at disease diagnosis. Although IgG4 staining was specific for EoE, it had a poor sensitivity with positive staining in only 48% of EoE patients. Further studies are warranted to fully elucidate the role of IgG4 in EoE.

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