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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Main Authors: Aldo Recinos, Tarik Zahouani, Juan Guillen, Benamanahalli Rajegowda
Format: Article
Language:English
Published: SAGE Publishing 2017-04-01
Series:Clinical Medicine Insights: Pediatrics
Online Access:https://doi.org/10.1177/1179556517702853
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spelling doaj-10fe1fa1f08b494abc38f2d729a1e7772020-11-25T03:09:23ZengSAGE PublishingClinical Medicine Insights: Pediatrics1179-55652017-04-011110.1177/117955651770285310.1177_1179556517702853Congenital Hepatic CystAldo RecinosTarik ZahouaniJuan GuillenBenamanahalli RajegowdaCongenital 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.https://doi.org/10.1177/1179556517702853
collection DOAJ
language English
format Article
sources DOAJ
author Aldo Recinos
Tarik Zahouani
Juan Guillen
Benamanahalli Rajegowda
spellingShingle Aldo Recinos
Tarik Zahouani
Juan Guillen
Benamanahalli Rajegowda
Congenital Hepatic Cyst
Clinical Medicine Insights: Pediatrics
author_facet Aldo Recinos
Tarik Zahouani
Juan Guillen
Benamanahalli Rajegowda
author_sort Aldo Recinos
title Congenital Hepatic Cyst
title_short Congenital Hepatic Cyst
title_full Congenital Hepatic Cyst
title_fullStr Congenital Hepatic Cyst
title_full_unstemmed Congenital Hepatic Cyst
title_sort congenital hepatic cyst
publisher SAGE Publishing
series Clinical Medicine Insights: Pediatrics
issn 1179-5565
publishDate 2017-04-01
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.
url https://doi.org/10.1177/1179556517702853
work_keys_str_mv AT aldorecinos congenitalhepaticcyst
AT tarikzahouani congenitalhepaticcyst
AT juanguillen congenitalhepaticcyst
AT benamanahallirajegowda congenitalhepaticcyst
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