A Rare Cause of Hepatomegaly: Infantile Hepatic Hemangiomendothelioma
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Case Report
VOLUME: 6 ISSUE: 3
P: 191 - 193
December 2016

A Rare Cause of Hepatomegaly: Infantile Hepatic Hemangiomendothelioma

J Acad Res Med 2016;6(3):191-193
1. Clinic of Pediatrics, Şişli Hamidiye Etfal Training and Research Hospital, İstanbul, Turkey
2. Clinic of Pediatrics Gastroenterology, Şişli Hamidiye Etfal Training and Research Hospital, İstanbul, Turkey
3. Clinic of Pediatrics Oncology, Şişli Hamidiye Etfal Training and Research Hospital, İstanbul, Turkey
No information available.
No information available
Received Date: 31.05.2015
Accepted Date: 13.07.2015
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ABSTRACT

Infantile hepatic hemangiomendothelioma, a bening vascular neoplasia derived from endothelial cells, is the most common newborn tumor located in the liver. The tumor has female predominancy. Mostly, it is associated with a good prognosis and may show spontaneous regression by the time the infant is 1 year of age. Although most of the patients are asymptomatic, abdominal mass, hepatomegaly, jaundice, nausea, and vomiting can be encountered among common clinical findings. Herein, a 1.5-month-old boy with abdominal distention was referred to our gastroenterology unit for hepatomegaly. Non-invasive diagnostic modalities revealed infantile hepatic hemangioendothelioma.

Keywords:
Infantile hemangiomendothelioma, liver, childhood