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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The Korean Society of Pediatric Hematology-Oncology
2019-04-01
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Online Access: | https://doi.org/10.15264/cpho.2019.26.1.60 |
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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 |
work_keys_str_mv |
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