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Idiopathic Adulthood Ductopenia Causing Cirrhosis

Idiopathic adulthood ductopenia (IAD) is a chronic small duct cholestatic biliary disease that is characterized by the loss of interlobular bile ducts. It is diagnosed when there is biochemical evidence of cholestatic liver disease, ductopenia on liver biopsy, and no other identifiable cause of chol...

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Autores principales: Douglass, Kevin M., Willner, Ira R., Glenn, Douglas J., Jones, Ryan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162123/
https://www.ncbi.nlm.nih.gov/pubmed/32337312
http://dx.doi.org/10.14309/crj.0000000000000349
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author Douglass, Kevin M.
Willner, Ira R.
Glenn, Douglas J.
Jones, Ryan M.
author_facet Douglass, Kevin M.
Willner, Ira R.
Glenn, Douglas J.
Jones, Ryan M.
author_sort Douglass, Kevin M.
collection PubMed
description Idiopathic adulthood ductopenia (IAD) is a chronic small duct cholestatic biliary disease that is characterized by the loss of interlobular bile ducts. It is diagnosed when there is biochemical evidence of cholestatic liver disease, ductopenia on liver biopsy, and no other identifiable cause of cholestasis. We present a patient with 10 days of progressive abdominal pain, jaundice, and worsening liver function tests who advanced to fulminant liver failure with no apparent underlying cause. He was found to have cirrhosis, with biopsy demonstrative of ductopenia, consistent with idiopathic adulthood ductopenia, which is a rare etiology of cirrhosis but should be considered when the typical workup yields no answer.
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spelling pubmed-71621232020-04-24 Idiopathic Adulthood Ductopenia Causing Cirrhosis Douglass, Kevin M. Willner, Ira R. Glenn, Douglas J. Jones, Ryan M. ACG Case Rep J Case Report Idiopathic adulthood ductopenia (IAD) is a chronic small duct cholestatic biliary disease that is characterized by the loss of interlobular bile ducts. It is diagnosed when there is biochemical evidence of cholestatic liver disease, ductopenia on liver biopsy, and no other identifiable cause of cholestasis. We present a patient with 10 days of progressive abdominal pain, jaundice, and worsening liver function tests who advanced to fulminant liver failure with no apparent underlying cause. He was found to have cirrhosis, with biopsy demonstrative of ductopenia, consistent with idiopathic adulthood ductopenia, which is a rare etiology of cirrhosis but should be considered when the typical workup yields no answer. Wolters Kluwer 2020-03-17 /pmc/articles/PMC7162123/ /pubmed/32337312 http://dx.doi.org/10.14309/crj.0000000000000349 Text en © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Case Report
Douglass, Kevin M.
Willner, Ira R.
Glenn, Douglas J.
Jones, Ryan M.
Idiopathic Adulthood Ductopenia Causing Cirrhosis
title Idiopathic Adulthood Ductopenia Causing Cirrhosis
title_full Idiopathic Adulthood Ductopenia Causing Cirrhosis
title_fullStr Idiopathic Adulthood Ductopenia Causing Cirrhosis
title_full_unstemmed Idiopathic Adulthood Ductopenia Causing Cirrhosis
title_short Idiopathic Adulthood Ductopenia Causing Cirrhosis
title_sort idiopathic adulthood ductopenia causing cirrhosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162123/
https://www.ncbi.nlm.nih.gov/pubmed/32337312
http://dx.doi.org/10.14309/crj.0000000000000349
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