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Congenital Hepatic Cyst

Congenital hepatic cyst is a rare and nonsymptomatic condition in infants and children. Its incidence is 2.5% in the postnatal life with a much lower incidence in the prenatal period. Incidental finding on antenatal imaging is the most common presentation. We present a case of a newborn in whom feta...

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Autores principales: Recinos, Aldo, Zahouani, Tarik, Guillen, Juan, Rajegowda, Benamanahalli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398644/
https://www.ncbi.nlm.nih.gov/pubmed/28469521
http://dx.doi.org/10.1177/1179556517702853
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author Recinos, Aldo
Zahouani, Tarik
Guillen, Juan
Rajegowda, Benamanahalli
author_facet Recinos, Aldo
Zahouani, Tarik
Guillen, Juan
Rajegowda, Benamanahalli
author_sort Recinos, Aldo
collection PubMed
description Congenital hepatic cyst is a rare and nonsymptomatic condition in infants and children. Its incidence is 2.5% in the postnatal life with a much lower incidence in the prenatal period. Incidental finding on antenatal imaging is the most common presentation. We present a case of a newborn in whom fetal ultrasound detected a cyst within the fetal liver. Postnatal imaging revealed a liver cyst in the right lobe of the liver, with no other intrahepatic structure affected. Liver function tests were abnormal, but the patient was asymptomatic. Posterior follow-up imaging showed a minor decrease in size. Management of congenital hepatic cyst is usually conservative, done with periodic ultrasound monitoring. However, surgical treatment is the mainstay of treatment when hydrops, progressive enlargement, hemorrhage, torsion, or compression of adjacent structures occurs. Malignant transformation can occur, but it is extremely rare. Partial or total removal of the cyst is the preferred treatment in neonates with a large lesion.
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spelling pubmed-53986442017-05-03 Congenital Hepatic Cyst Recinos, Aldo Zahouani, Tarik Guillen, Juan Rajegowda, Benamanahalli Clin Med Insights Pediatr Case Report Congenital hepatic cyst is a rare and nonsymptomatic condition in infants and children. Its incidence is 2.5% in the postnatal life with a much lower incidence in the prenatal period. Incidental finding on antenatal imaging is the most common presentation. We present a case of a newborn in whom fetal ultrasound detected a cyst within the fetal liver. Postnatal imaging revealed a liver cyst in the right lobe of the liver, with no other intrahepatic structure affected. Liver function tests were abnormal, but the patient was asymptomatic. Posterior follow-up imaging showed a minor decrease in size. Management of congenital hepatic cyst is usually conservative, done with periodic ultrasound monitoring. However, surgical treatment is the mainstay of treatment when hydrops, progressive enlargement, hemorrhage, torsion, or compression of adjacent structures occurs. Malignant transformation can occur, but it is extremely rare. Partial or total removal of the cyst is the preferred treatment in neonates with a large lesion. SAGE Publications 2017-04-10 /pmc/articles/PMC5398644/ /pubmed/28469521 http://dx.doi.org/10.1177/1179556517702853 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (http://www.uk.sagepub.com/aboutus/openaccess.htm).
spellingShingle Case Report
Recinos, Aldo
Zahouani, Tarik
Guillen, Juan
Rajegowda, Benamanahalli
Congenital Hepatic Cyst
title Congenital Hepatic Cyst
title_full Congenital Hepatic Cyst
title_fullStr Congenital Hepatic Cyst
title_full_unstemmed Congenital Hepatic Cyst
title_short Congenital Hepatic Cyst
title_sort congenital hepatic cyst
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398644/
https://www.ncbi.nlm.nih.gov/pubmed/28469521
http://dx.doi.org/10.1177/1179556517702853
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