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Polycystic liver disease presenting as pruritus
Polycystic liver disease (PCLD) is a rare autosomal dominant disorder which usually occurs in association with autosomal dominant polycystic kidney disease. Biliary obstruction is a rare complication of PCLD. Treatment options include percutaneous aspiration and sclerosis, surgical deroofing of cyst...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hellenic Society of Gastroenterology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3959546/ https://www.ncbi.nlm.nih.gov/pubmed/24714704 |
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author | Johnson, Deepak Kochummen Panchili, Shihab Kolasseri, Sandesh Mavali, Ramachandran Thazhath |
author_facet | Johnson, Deepak Kochummen Panchili, Shihab Kolasseri, Sandesh Mavali, Ramachandran Thazhath |
author_sort | Johnson, Deepak Kochummen |
collection | PubMed |
description | Polycystic liver disease (PCLD) is a rare autosomal dominant disorder which usually occurs in association with autosomal dominant polycystic kidney disease. Biliary obstruction is a rare complication of PCLD. Treatment options include percutaneous aspiration and sclerosis, surgical deroofing of cysts, liver resection or liver transplantation. Medical treatment involves the use of somatostatin analogues or mTOR inhibitors. We present a case of PCLD presenting for the first time with longstanding pruritus as the only symptom. |
format | Online Article Text |
id | pubmed-3959546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hellenic Society of Gastroenterology |
record_format | MEDLINE/PubMed |
spelling | pubmed-39595462014-04-07 Polycystic liver disease presenting as pruritus Johnson, Deepak Kochummen Panchili, Shihab Kolasseri, Sandesh Mavali, Ramachandran Thazhath Ann Gastroenterol Case Report Polycystic liver disease (PCLD) is a rare autosomal dominant disorder which usually occurs in association with autosomal dominant polycystic kidney disease. Biliary obstruction is a rare complication of PCLD. Treatment options include percutaneous aspiration and sclerosis, surgical deroofing of cysts, liver resection or liver transplantation. Medical treatment involves the use of somatostatin analogues or mTOR inhibitors. We present a case of PCLD presenting for the first time with longstanding pruritus as the only symptom. Hellenic Society of Gastroenterology 2014 /pmc/articles/PMC3959546/ /pubmed/24714704 Text en Copyright: © Hellenic Society of Gastroenterology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Johnson, Deepak Kochummen Panchili, Shihab Kolasseri, Sandesh Mavali, Ramachandran Thazhath Polycystic liver disease presenting as pruritus |
title | Polycystic liver disease presenting as pruritus |
title_full | Polycystic liver disease presenting as pruritus |
title_fullStr | Polycystic liver disease presenting as pruritus |
title_full_unstemmed | Polycystic liver disease presenting as pruritus |
title_short | Polycystic liver disease presenting as pruritus |
title_sort | polycystic liver disease presenting as pruritus |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3959546/ https://www.ncbi.nlm.nih.gov/pubmed/24714704 |
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