Cargando…

Partial Internal Biliary Diversion: A Solution for Intractable Pruritus in Progressive Familial Intrahepatic Cholestasis Type 1

Biliary diversion offers a potential option for intractable pruritus in children with chronic cholestatic disorders. Progressive familial intrahepatic cholestasis (PFIC) is an inherited disorder of impaired bile acid transport and excretion, which presents with jaundice and pruritus in the first few...

Descripción completa

Detalles Bibliográficos
Autores principales: Ganesh, Ramaswamy, Suresh, Natarajan, Sathiyasekeran, Malathi, Ramachandran, Priya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122094/
https://www.ncbi.nlm.nih.gov/pubmed/21546727
http://dx.doi.org/10.4103/1319-3767.80387
_version_ 1782206895869657088
author Ganesh, Ramaswamy
Suresh, Natarajan
Sathiyasekeran, Malathi
Ramachandran, Priya
author_facet Ganesh, Ramaswamy
Suresh, Natarajan
Sathiyasekeran, Malathi
Ramachandran, Priya
author_sort Ganesh, Ramaswamy
collection PubMed
description Biliary diversion offers a potential option for intractable pruritus in children with chronic cholestatic disorders. Progressive familial intrahepatic cholestasis (PFIC) is an inherited disorder of impaired bile acid transport and excretion, which presents with jaundice and pruritus in the first few months of life and progresses to cirrhosis by infancy or adolescence. We report a child with PFIC type 1 who underwent internal biliary diversion for intractable pruritus and was relieved of his symptoms.
format Online
Article
Text
id pubmed-3122094
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Medknow Publications
record_format MEDLINE/PubMed
spelling pubmed-31220942011-07-01 Partial Internal Biliary Diversion: A Solution for Intractable Pruritus in Progressive Familial Intrahepatic Cholestasis Type 1 Ganesh, Ramaswamy Suresh, Natarajan Sathiyasekeran, Malathi Ramachandran, Priya Saudi J Gastroenterol Case Report Biliary diversion offers a potential option for intractable pruritus in children with chronic cholestatic disorders. Progressive familial intrahepatic cholestasis (PFIC) is an inherited disorder of impaired bile acid transport and excretion, which presents with jaundice and pruritus in the first few months of life and progresses to cirrhosis by infancy or adolescence. We report a child with PFIC type 1 who underwent internal biliary diversion for intractable pruritus and was relieved of his symptoms. Medknow Publications 2011 /pmc/articles/PMC3122094/ /pubmed/21546727 http://dx.doi.org/10.4103/1319-3767.80387 Text en © Saudi Journal of Gastroenterology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ganesh, Ramaswamy
Suresh, Natarajan
Sathiyasekeran, Malathi
Ramachandran, Priya
Partial Internal Biliary Diversion: A Solution for Intractable Pruritus in Progressive Familial Intrahepatic Cholestasis Type 1
title Partial Internal Biliary Diversion: A Solution for Intractable Pruritus in Progressive Familial Intrahepatic Cholestasis Type 1
title_full Partial Internal Biliary Diversion: A Solution for Intractable Pruritus in Progressive Familial Intrahepatic Cholestasis Type 1
title_fullStr Partial Internal Biliary Diversion: A Solution for Intractable Pruritus in Progressive Familial Intrahepatic Cholestasis Type 1
title_full_unstemmed Partial Internal Biliary Diversion: A Solution for Intractable Pruritus in Progressive Familial Intrahepatic Cholestasis Type 1
title_short Partial Internal Biliary Diversion: A Solution for Intractable Pruritus in Progressive Familial Intrahepatic Cholestasis Type 1
title_sort partial internal biliary diversion: a solution for intractable pruritus in progressive familial intrahepatic cholestasis type 1
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3122094/
https://www.ncbi.nlm.nih.gov/pubmed/21546727
http://dx.doi.org/10.4103/1319-3767.80387
work_keys_str_mv AT ganeshramaswamy partialinternalbiliarydiversionasolutionforintractablepruritusinprogressivefamilialintrahepaticcholestasistype1
AT sureshnatarajan partialinternalbiliarydiversionasolutionforintractablepruritusinprogressivefamilialintrahepaticcholestasistype1
AT sathiyasekeranmalathi partialinternalbiliarydiversionasolutionforintractablepruritusinprogressivefamilialintrahepaticcholestasistype1
AT ramachandranpriya partialinternalbiliarydiversionasolutionforintractablepruritusinprogressivefamilialintrahepaticcholestasistype1