Congenital Hepatic Arteriovenous Malformation Presenting as Isolated Massive Hepatomegaly in an Otherwise Healthy Neonate: A Case Report

Congenital hepatic arteriovenous malformations (HAVMs), though rare, carry high morbidity and mortality rates if left undiagnosed. The usual clinical presentation is in infancy with congestive heart failure, anaemia and hepatomegaly. There are reports of presentation as persistent pulmonary hyperten...

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Autores principales: Tiwari, Charu, Nagdeve, Nilesh, Saoji, Rajendra, Hatwar, Ghanshyam, Sinha, Sanskriti, Thatte, Sharvil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518103/
https://www.ncbi.nlm.nih.gov/pubmed/33074180
http://dx.doi.org/10.34763/jmotherandchild.2020241.2002.000008
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author Tiwari, Charu
Nagdeve, Nilesh
Saoji, Rajendra
Hatwar, Ghanshyam
Sinha, Sanskriti
Thatte, Sharvil
author_facet Tiwari, Charu
Nagdeve, Nilesh
Saoji, Rajendra
Hatwar, Ghanshyam
Sinha, Sanskriti
Thatte, Sharvil
author_sort Tiwari, Charu
collection PubMed
description Congenital hepatic arteriovenous malformations (HAVMs), though rare, carry high morbidity and mortality rates if left undiagnosed. The usual clinical presentation is in infancy with congestive heart failure, anaemia and hepatomegaly. There are reports of presentation as persistent pulmonary hypertension in newborns and reports of their spontaneous regression as well. We describe a healthy full-term neonate with HAVM who was presented with isolated massive hepatomegaly and underwent surgical ligation.
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spelling pubmed-85181032021-11-23 Congenital Hepatic Arteriovenous Malformation Presenting as Isolated Massive Hepatomegaly in an Otherwise Healthy Neonate: A Case Report Tiwari, Charu Nagdeve, Nilesh Saoji, Rajendra Hatwar, Ghanshyam Sinha, Sanskriti Thatte, Sharvil J Mother Child Case Report Congenital hepatic arteriovenous malformations (HAVMs), though rare, carry high morbidity and mortality rates if left undiagnosed. The usual clinical presentation is in infancy with congestive heart failure, anaemia and hepatomegaly. There are reports of presentation as persistent pulmonary hypertension in newborns and reports of their spontaneous regression as well. We describe a healthy full-term neonate with HAVM who was presented with isolated massive hepatomegaly and underwent surgical ligation. Sciendo 2020-07-29 /pmc/articles/PMC8518103/ /pubmed/33074180 http://dx.doi.org/10.34763/jmotherandchild.2020241.2002.000008 Text en © 2020 Charu Tiwari et al., published by Sciendo https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Case Report
Tiwari, Charu
Nagdeve, Nilesh
Saoji, Rajendra
Hatwar, Ghanshyam
Sinha, Sanskriti
Thatte, Sharvil
Congenital Hepatic Arteriovenous Malformation Presenting as Isolated Massive Hepatomegaly in an Otherwise Healthy Neonate: A Case Report
title Congenital Hepatic Arteriovenous Malformation Presenting as Isolated Massive Hepatomegaly in an Otherwise Healthy Neonate: A Case Report
title_full Congenital Hepatic Arteriovenous Malformation Presenting as Isolated Massive Hepatomegaly in an Otherwise Healthy Neonate: A Case Report
title_fullStr Congenital Hepatic Arteriovenous Malformation Presenting as Isolated Massive Hepatomegaly in an Otherwise Healthy Neonate: A Case Report
title_full_unstemmed Congenital Hepatic Arteriovenous Malformation Presenting as Isolated Massive Hepatomegaly in an Otherwise Healthy Neonate: A Case Report
title_short Congenital Hepatic Arteriovenous Malformation Presenting as Isolated Massive Hepatomegaly in an Otherwise Healthy Neonate: A Case Report
title_sort congenital hepatic arteriovenous malformation presenting as isolated massive hepatomegaly in an otherwise healthy neonate: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518103/
https://www.ncbi.nlm.nih.gov/pubmed/33074180
http://dx.doi.org/10.34763/jmotherandchild.2020241.2002.000008
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