Prediction of esophageal and gastric histology by macroscopic diagnosis during upper endoscopy in pediatric celiac disease

AIM To determine the sensitivity of macroscopic appearance for predicting histological diagnosis at sites other than duodenum in pediatric celiac disease(CD).METHODS Endoscopic and histologic findings in pediatric patients undergoing upper endoscopy for first-time diagnosis of CD at Stollery Childre...

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Published inWorld journal of gastroenterology : WJG Vol. 23; no. 4; pp. 646 - 652
Main Authors Boschee, Erin D, Yap, Jason Y K, Turner, Justine M
Format Journal Article
LanguageEnglish
Published United States Baishideng Publishing Group Inc 28.01.2017
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Summary:AIM To determine the sensitivity of macroscopic appearance for predicting histological diagnosis at sites other than duodenum in pediatric celiac disease(CD).METHODS Endoscopic and histologic findings in pediatric patients undergoing upper endoscopy for first-time diagnosis of CD at Stollery Children’s Hospital from 2010-2012 were retrospectively reviewed.RESULTS Clinical charts from 140 patients were reviewed. Esophageal and gastric biopsies were taken in 54.3% and 77.9% of patients, respectively. Endoscopic appearance was normal in the esophagus and stomach in 75% and 86.2%. Endoscopic esophageal diagnoses were eosinophilic esophagitis(EE)(11.8%), esophagitis(7.9%), glycogenic acanthosis(1.3%) and non-specific abnormalities(3.9%). Endoscopic gastric diagnoses were gastritis(8.3%), pancreatic rest(0.9%), and nonspecific abnormalities(4.6%). Histology was normal in 76.3% of esophageal and 87.2% of gastric speci-mens. Abnormal esophageal histology was EE(10.5%), esophagitis(10.5%), glycogenic acanthosis(1.3%) and non-specific(1.3%). Gastritis was reported in 12.8% of specimens. Sensitivity and specificity of normal endoscopy for predicting normal esophageal histology was 86.2% and 61.1%, and for normal gastric histology was 87.4% and 21.4%.CONCLUSION In the absence of macroscopic abnormalities, routine esophageal and gastric biopsy during endoscopy for pediatric CD does not identify major pathologies. These findings have cost and time saving implications for clinical practice.
Bibliography:Erin D Boschee;Jason YK Yap;Justine M Turner;Department of Alberta;Edmonton Clinic Health Academy,University of Alberta Hospital;Division of Pediatric Gastroenterology, Department of Pediatrics, University of Alberta
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Author contributions: Boschee ED helped to design the research, performed the data collection and analysis, and wrote the manuscript; Yap JYK and Turner JM helped to design and supervise the project.
Supported by Women and Children’s Health Research Institute.
Correspondence to: Erin D Boschee, MD, BSc (Hons), Department of Pediatrics, University of Alberta, 8440 112 Street NW, Edmonton, Alberta T6G 2B7, Canada. boschee@ualberta.ca
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.v23.i4.646