Comparison of Endoscopic and Histological Findings between Typical and Atypical Celiac Disease in Children
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Purpose: Celiac disease is a common non-communicable disease with varied presentations. Purpose of this study was to find the duodeno-endoscopic features in celiac disease and to compare duodeno-endoscopic and histological findings between typical and atypical celiac disease in children. Methods: Hospital based observational study was conducted at Sir Padampat Mother and Child Health Institute, Jaipur from June 2015 to May 2016. Patients were selected and divided in two groups- typical and atypical celiac disease based upon the presenting symptoms. Upper gastrointestinal endoscopy and duodenal biopsy was per-formed for serology positive patients. Results were analysed using appropriate statistical test of significance.Results: Out of 101 enrolled patients, 47.5% were male. Age ranged from 1 to 18 years. Study showed that 54.5% were typical and 45.5% were atypical. Patients presenting with atypical symptoms were predominantly of older age group. On endoscopy, scalloping, mosaic pattern, reduced fold height and absent fold height; and in histology, ad-vanced Marsh stage were significantly higher in the typical group. Conclusion: Awareness of atypical presentations as well as duodeno-endoscopic features may have considerable practical importance for the diagnosis of celiac disease in children. Scalloping, mosaic pattern, reduced fold height and nodularity are main endoscopic markers of celiac disease in children. Endoscopic markers of duodenal mucosa may be important in early diagnosis of celiac disease, in children subjected to endoscopy for atypical presentations or indication other than suspected celiac disease.
Abstract
Purpose: Celiac disease is a common non-communicable disease with varied presentations. Purpose of this study was to find the duodeno-endoscopic features in celiac disease and to compare duodeno-endoscopic and histological findings between typical and atypical celiac disease in children. Methods: Hospital based observational study was conducted at Sir Padampat Mother and Child Health Institute, Jaipur from June 2015 to May 2016. Patients were selected and divided in two groups- typical and atypical celiac disease based upon the presenting symptoms. Upper gastrointestinal endoscopy and duodenal biopsy was per-formed for serology positive patients. Results were analysed using appropriate statistical test of significance.Results: Out of 101 enrolled patients, 47.5% were male. Age ranged from 1 to 18 years. Study showed that 54.5% were typical and 45.5% were atypical. Patients presenting with atypical symptoms were predominantly of older age group. On endoscopy, scalloping, mosaic pattern, reduced fold height and absent fold height; and in histology, ad-vanced Marsh stage were significantly higher in the typical group. Conclusion: Awareness of atypical presentations as well as duodeno-endoscopic features may have considerable practical importance for the diagnosis of celiac disease in children. Scalloping, mosaic pattern, reduced fold height and nodularity are main endoscopic markers of celiac disease in children. Endoscopic markers of duodenal mucosa may be important in early diagnosis of celiac disease, in children subjected to endoscopy for atypical presentations or indication other than suspected celiac disease.
참고문헌 (20)
- Husby S, "European Society for Pediatric Gastroenterology, Hepatology, and Nutrition guidelines for the diagnosis of coeliac disease", J Pediatr Gastroenterol Nutr, 54, pp.136~160 (2012)[DOI]
- Lionetti E, "New clues in celiac disease epidemiology, pathogenesis, clinical manifestations, and treatment", Int Rev Immunol, 30, pp.219~231 (2011)[DOI]
- Branski D, "Nelson textbook of pediatrics", pp.1835~1838 (2016), Elsevier Saunders
- Dinler G, "Celiac disease in 87 children with typical and atypical symptoms in Black Sea region of Turkey", World J Pediatr, 5, pp.282~286 (2009)[DOI]
- Guandalini S, "Textbook of pediatric gastroenterology and nutrition", pp.435~450 (2004), Taylor & Francis
- Sharma A, "Time to recognize atypical celiac disease in Indian children", Indian J Gastroenterol, 26, pp.269~273 (2007)
- Garg K, "What a practitioner needs to know about celiac disease?", Indian J Pediatr, 82, pp.145~151 (2015)[DOI]
- Balaban DV, "Diagnostic yield of endoscopic markers for celiac disease", J Med Life, 8, pp.452~457 (2015)
- Ravelli AM, "Endoscopic features of celiac disease in children", Gastrointest Endosc, 54, pp.736~742 (2001)[DOI]
- Rosa RM, "Correlation of endoscopic and histological features in adults with suspected celiac disease in a referral center of Minas Gerais, Brazil", Arq Gastroenterol, 51, pp.290~296 (2014)[DOI]
- Corazza GR, "Scalloped duodenal folds in childhood celiac disease", Gastrointest Endosc, 39, pp.543~545 (1993)[DOI]
- Kasirer Y, "Scalloping is a reliable endoscopic marker for celiac disease", Dig Endosc, 26, pp.232~235 (2014)[DOI]
- Oberhuber G, "The histopathology of coeliac disease: time for a standardized report scheme for pathologists", Eur J Gastroenterol Hepatol, 11, pp.1185~1194 (1999)
- Poddar U, "Pediatric and adult celiac disease: similarities and differences", Indian J Gastroenterol, 32, pp.283~288 (2013)[DOI]
- Gupta R, "Indian task force for celiac disease: current status", World J Gastroenterol, 15, pp.6028~6033 (2009)[DOI]
- Zarife Kulo lu, "Celiac Disease: Presentation of 109 Children", Yonsei Medical Journal, 50(5), pp.617~623 (2009), 연세대학교의과대학
- Savas N, "Correlation of clinical and histopathological with endoscopic findings of celiac disease in the Turkish population", Dig Dis Sci, 52, pp.1299~1303 (2007)[DOI]
- Piazzi L, "Diagnostic value of endoscopic markers for celiac disease in adults: a multicentre prospective Italian study", Minerva Gastroenterol Dietol, 54, pp.335~346 (2008)
- Tursi A, "Endoscopic features of celiac disease in adults and their correlation with age, histological damage, and clinical form of the disease", Endoscopy, 34, pp.787~792 (2002)[DOI]
- Brar P, "Lack of correlation of degree of villous atrophy with severity of clinical presentation of coeliac disease", Dig Liver Dis, 39, pp.26~29 (2007)[DOI]
