Primary Cardiac Hemangioendothelioma in an Infant: A Case Report

Primary cardiac tumors are rare, with a prevalence of 0.001-0.2%. Among such tumors, cardiac hemangioendotheliomas are some of the most uncommon. In Korea, there have been no reports of hemangioendothelioma occurring in the heart of infants. We herein report a case of an infant that was admitted to...

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Main Authors: Jeong-wook Seo, Mi Kyoung Song, Sung-hye Park, Hye Eun Park, Sin Ae Park
Format: Article
Language:English
Published: The Korean Society of Pediatric Hematology-Oncology 2019-04-01
Series:Clinical Pediatric Hematology-Oncology
Subjects:
Online Access:https://doi.org/10.15264/cpho.2019.26.1.60
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spelling doaj-d8be8a0daaa74a54bd73553cb64989be2020-11-25T02:25:04ZengThe Korean Society of Pediatric Hematology-OncologyClinical Pediatric Hematology-Oncology2233-52502019-04-01261606510.15264/cpho.2019.26.1.60cpho.2019.26.1.60Primary Cardiac Hemangioendothelioma in an Infant: A Case ReportJeong-wook Seo0Mi Kyoung Song1Sung-hye Park2Hye Eun Park3Sin Ae Park4Presbyterian Medical Center, Jeonju, KoreaDepartment of Pediatrics, Seoul National University Children’s Hospital, Seoul, KoreaDepartment of Pathology, Seoul National University College of Medicine, Seoul, KoreaDepartment of Pathology, Seoul National University College of Medicine, Seoul, KoreaPresbyterian Medical Center, Jeonju, KoreaPrimary cardiac tumors are rare, with a prevalence of 0.001-0.2%. Among such tumors, cardiac hemangioendotheliomas are some of the most uncommon. In Korea, there have been no reports of hemangioendothelioma occurring in the heart of infants. We herein report a case of an infant that was admitted to our medical center and presented with cough and a runny nose. The initial diagnosis was acute bronchiolitis. Cardiomegaly was observed on chest radiography. Echocardiography revealed a tumor measuring 3.5×4.0 cm in the right atrium. The infant was transferred to a tertiary medical center for tumor excision. The excised lesion was 3.8×3×3.2 cm in size, and biopsy confirmed a diagnosis of hemangioendothelioma. In this case report, we describe our experience with a rare case involving cardiac tumor in an infant with an upper respiratory tract infection.https://doi.org/10.15264/cpho.2019.26.1.60hemangioendotheliomaheartinfanttwins
collection DOAJ
language English
format Article
sources DOAJ
author Jeong-wook Seo
Mi Kyoung Song
Sung-hye Park
Hye Eun Park
Sin Ae Park
spellingShingle Jeong-wook Seo
Mi Kyoung Song
Sung-hye Park
Hye Eun Park
Sin Ae Park
Primary Cardiac Hemangioendothelioma in an Infant: A Case Report
Clinical Pediatric Hematology-Oncology
hemangioendothelioma
heart
infant
twins
author_facet Jeong-wook Seo
Mi Kyoung Song
Sung-hye Park
Hye Eun Park
Sin Ae Park
author_sort Jeong-wook Seo
title Primary Cardiac Hemangioendothelioma in an Infant: A Case Report
title_short Primary Cardiac Hemangioendothelioma in an Infant: A Case Report
title_full Primary Cardiac Hemangioendothelioma in an Infant: A Case Report
title_fullStr Primary Cardiac Hemangioendothelioma in an Infant: A Case Report
title_full_unstemmed Primary Cardiac Hemangioendothelioma in an Infant: A Case Report
title_sort primary cardiac hemangioendothelioma in an infant: a case report
publisher The Korean Society of Pediatric Hematology-Oncology
series Clinical Pediatric Hematology-Oncology
issn 2233-5250
publishDate 2019-04-01
description Primary cardiac tumors are rare, with a prevalence of 0.001-0.2%. Among such tumors, cardiac hemangioendotheliomas are some of the most uncommon. In Korea, there have been no reports of hemangioendothelioma occurring in the heart of infants. We herein report a case of an infant that was admitted to our medical center and presented with cough and a runny nose. The initial diagnosis was acute bronchiolitis. Cardiomegaly was observed on chest radiography. Echocardiography revealed a tumor measuring 3.5×4.0 cm in the right atrium. The infant was transferred to a tertiary medical center for tumor excision. The excised lesion was 3.8×3×3.2 cm in size, and biopsy confirmed a diagnosis of hemangioendothelioma. In this case report, we describe our experience with a rare case involving cardiac tumor in an infant with an upper respiratory tract infection.
topic hemangioendothelioma
heart
infant
twins
url https://doi.org/10.15264/cpho.2019.26.1.60
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