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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Published in | Clinical pediatric hematology-oncology Vol. 26; no. 1; pp. 60 - 65 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
The Korean Society of Pediatric Hematology-Oncology
01.04.2019
대한소아혈액종양학회 |
Subjects | |
Online Access | Get full text |
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Summary: | 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. |
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ISSN: | 2233-5250 2233-5250 |
DOI: | 10.15264/cpho.2019.26.1.60 |