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Autoimmune Sclerosing Cholangitis in Children: A Prospective Case-Control Study

PURPOSE: In children overlap of autoimmune hepatitis (AIH) and primary sclerosing cholangitis is labelled as autoimmune sclerosing cholangitis (ASC). The only prospective pediatric study showed a high prevalence of ASC by using endoscopic retrograde cholangiopancreatography. Aims of our study were t...

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Autores principales: Kumar, Nagendra, Poddar, Ujjal, Yadav, Rajnikant, Lal, Hira, Pani, Krushna, Yachha, Surender Kumar, Srivastava, Anshu, Pandey, Rakesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007839/
https://www.ncbi.nlm.nih.gov/pubmed/33833971
http://dx.doi.org/10.5223/pghn.2021.24.2.154
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author Kumar, Nagendra
Poddar, Ujjal
Yadav, Rajnikant
Lal, Hira
Pani, Krushna
Yachha, Surender Kumar
Srivastava, Anshu
Pandey, Rakesh
author_facet Kumar, Nagendra
Poddar, Ujjal
Yadav, Rajnikant
Lal, Hira
Pani, Krushna
Yachha, Surender Kumar
Srivastava, Anshu
Pandey, Rakesh
author_sort Kumar, Nagendra
collection PubMed
description PURPOSE: In children overlap of autoimmune hepatitis (AIH) and primary sclerosing cholangitis is labelled as autoimmune sclerosing cholangitis (ASC). The only prospective pediatric study showed a high prevalence of ASC by using endoscopic retrograde cholangiopancreatography. Aims of our study were to find the prevalence of ASC by using magnetic resonance cholangiography (MRC) in AIH and in non-AIH cirrhosis and to compare clinical presentation and outcome of AIH and ASC. METHODS: Prospectively we did MRC in 38 children with AIH (cases) and 19 disease controls (Wilson disease). Multiple biliary strictures with proximal dilatation on MRC were taken as definitive changes of ASC. Detail clinical, laboratory parameters, liver histopathology and treatment outcome were recorded. RESULTS: The median age of cases was 11.5 (3–18) years, 22 (57.9%) were girls and 28 (73.7%) were diagnosed as type 1 AIH. MRC was done in 11 children (28.9%) at the time of diagnosis and in 27 (71.1%) after a median follow-up of 2.5 (0.3–10) years. Abnormal MRC changes were seen in 14/38 (36.8%) of AIH and 8/19 (42.1%) of controls. However, definite changes of ASC were present in four (10.5%) children in AIH and none in controls. None of the clinical, laboratory, histological parameters and treatment response were significantly different between ASC and AIH groups. CONCLUSION: The prevalence of ASC in children with AIH was just 10.5%. We suggest MRC in select group with cholestatic features, inflammatory bowel disease and in those who showed poor response to immunosuppression instead of all children with AIH.
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spelling pubmed-80078392021-04-07 Autoimmune Sclerosing Cholangitis in Children: A Prospective Case-Control Study Kumar, Nagendra Poddar, Ujjal Yadav, Rajnikant Lal, Hira Pani, Krushna Yachha, Surender Kumar Srivastava, Anshu Pandey, Rakesh Pediatr Gastroenterol Hepatol Nutr Original Article PURPOSE: In children overlap of autoimmune hepatitis (AIH) and primary sclerosing cholangitis is labelled as autoimmune sclerosing cholangitis (ASC). The only prospective pediatric study showed a high prevalence of ASC by using endoscopic retrograde cholangiopancreatography. Aims of our study were to find the prevalence of ASC by using magnetic resonance cholangiography (MRC) in AIH and in non-AIH cirrhosis and to compare clinical presentation and outcome of AIH and ASC. METHODS: Prospectively we did MRC in 38 children with AIH (cases) and 19 disease controls (Wilson disease). Multiple biliary strictures with proximal dilatation on MRC were taken as definitive changes of ASC. Detail clinical, laboratory parameters, liver histopathology and treatment outcome were recorded. RESULTS: The median age of cases was 11.5 (3–18) years, 22 (57.9%) were girls and 28 (73.7%) were diagnosed as type 1 AIH. MRC was done in 11 children (28.9%) at the time of diagnosis and in 27 (71.1%) after a median follow-up of 2.5 (0.3–10) years. Abnormal MRC changes were seen in 14/38 (36.8%) of AIH and 8/19 (42.1%) of controls. However, definite changes of ASC were present in four (10.5%) children in AIH and none in controls. None of the clinical, laboratory, histological parameters and treatment response were significantly different between ASC and AIH groups. CONCLUSION: The prevalence of ASC in children with AIH was just 10.5%. We suggest MRC in select group with cholestatic features, inflammatory bowel disease and in those who showed poor response to immunosuppression instead of all children with AIH. The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2021-03 2021-03-08 /pmc/articles/PMC8007839/ /pubmed/33833971 http://dx.doi.org/10.5223/pghn.2021.24.2.154 Text en Copyright © 2021 by The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition https://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kumar, Nagendra
Poddar, Ujjal
Yadav, Rajnikant
Lal, Hira
Pani, Krushna
Yachha, Surender Kumar
Srivastava, Anshu
Pandey, Rakesh
Autoimmune Sclerosing Cholangitis in Children: A Prospective Case-Control Study
title Autoimmune Sclerosing Cholangitis in Children: A Prospective Case-Control Study
title_full Autoimmune Sclerosing Cholangitis in Children: A Prospective Case-Control Study
title_fullStr Autoimmune Sclerosing Cholangitis in Children: A Prospective Case-Control Study
title_full_unstemmed Autoimmune Sclerosing Cholangitis in Children: A Prospective Case-Control Study
title_short Autoimmune Sclerosing Cholangitis in Children: A Prospective Case-Control Study
title_sort autoimmune sclerosing cholangitis in children: a prospective case-control study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007839/
https://www.ncbi.nlm.nih.gov/pubmed/33833971
http://dx.doi.org/10.5223/pghn.2021.24.2.154
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