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Severe Hepatopulmonary Syndrome in a Child with Caroli Syndrome

Hepatopulmonary Syndrome (HPS) is a potential complication of chronic liver disease and is more commonly seen in the adult population. Caroli Syndrome is a rare inherited disorder characterized by intrahepatic ductal dilation and liver fibrosis that leads to portal hypertension. In children with liv...

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Autores principales: De Jesus-Rojas, W., McBeth, K., Yadav, A., Stark, J. M., Mosquera, R. A., Jon, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5572614/
https://www.ncbi.nlm.nih.gov/pubmed/28884036
http://dx.doi.org/10.1155/2017/2171974
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author De Jesus-Rojas, W.
McBeth, K.
Yadav, A.
Stark, J. M.
Mosquera, R. A.
Jon, C.
author_facet De Jesus-Rojas, W.
McBeth, K.
Yadav, A.
Stark, J. M.
Mosquera, R. A.
Jon, C.
author_sort De Jesus-Rojas, W.
collection PubMed
description Hepatopulmonary Syndrome (HPS) is a potential complication of chronic liver disease and is more commonly seen in the adult population. Caroli Syndrome is a rare inherited disorder characterized by intrahepatic ductal dilation and liver fibrosis that leads to portal hypertension. In children with liver disease, HPS should be considered in the differential diagnosis of prolonged, otherwise unexplained, hypoxemia. The presence of HPS can improve patient priority on the liver transplantation wait list, despite their Pediatric End-Stage Liver Disease (PELD) score. We present a 6-year-old girl with Caroli Syndrome and End-Stage Renal Disease who presented with persistent hypoxemia. The goal of this report is to increase awareness of HPS in children.
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spelling pubmed-55726142017-09-07 Severe Hepatopulmonary Syndrome in a Child with Caroli Syndrome De Jesus-Rojas, W. McBeth, K. Yadav, A. Stark, J. M. Mosquera, R. A. Jon, C. Case Rep Pediatr Case Report Hepatopulmonary Syndrome (HPS) is a potential complication of chronic liver disease and is more commonly seen in the adult population. Caroli Syndrome is a rare inherited disorder characterized by intrahepatic ductal dilation and liver fibrosis that leads to portal hypertension. In children with liver disease, HPS should be considered in the differential diagnosis of prolonged, otherwise unexplained, hypoxemia. The presence of HPS can improve patient priority on the liver transplantation wait list, despite their Pediatric End-Stage Liver Disease (PELD) score. We present a 6-year-old girl with Caroli Syndrome and End-Stage Renal Disease who presented with persistent hypoxemia. The goal of this report is to increase awareness of HPS in children. Hindawi 2017 2017-08-13 /pmc/articles/PMC5572614/ /pubmed/28884036 http://dx.doi.org/10.1155/2017/2171974 Text en Copyright © 2017 W. De Jesus-Rojas et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under 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
De Jesus-Rojas, W.
McBeth, K.
Yadav, A.
Stark, J. M.
Mosquera, R. A.
Jon, C.
Severe Hepatopulmonary Syndrome in a Child with Caroli Syndrome
title Severe Hepatopulmonary Syndrome in a Child with Caroli Syndrome
title_full Severe Hepatopulmonary Syndrome in a Child with Caroli Syndrome
title_fullStr Severe Hepatopulmonary Syndrome in a Child with Caroli Syndrome
title_full_unstemmed Severe Hepatopulmonary Syndrome in a Child with Caroli Syndrome
title_short Severe Hepatopulmonary Syndrome in a Child with Caroli Syndrome
title_sort severe hepatopulmonary syndrome in a child with caroli syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5572614/
https://www.ncbi.nlm.nih.gov/pubmed/28884036
http://dx.doi.org/10.1155/2017/2171974
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