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Primary Cardiac Hemangioendothelioma in an Infant: A Case Report / 임상소아혈액종양
Clinical Pediatric Hematology-Oncology ; : 60-65, 2019.
Article in English | WPRIM | ID: wpr-763503
ABSTRACT
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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Full text: Available Index: WPRIM (Western Pacific) Main subject: Respiratory Tract Infections / Thorax / Twins / Biopsy / Bronchiolitis / Echocardiography / Radiography / Nose / Prevalence / Cardiomegaly Type of study: Diagnostic study / Prevalence study Limits: Humans / Infant Country/Region as subject: Asia Language: English Journal: Clinical Pediatric Hematology-Oncology Year: 2019 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Respiratory Tract Infections / Thorax / Twins / Biopsy / Bronchiolitis / Echocardiography / Radiography / Nose / Prevalence / Cardiomegaly Type of study: Diagnostic study / Prevalence study Limits: Humans / Infant Country/Region as subject: Asia Language: English Journal: Clinical Pediatric Hematology-Oncology Year: 2019 Type: Article