Abstract
ABSTRACT Congenital hepatic arteriovenous malformation (HAVM) is an uncommonly encountered condition in clinical practice. This condition often presents as isolated hepatomegaly, congestive cardiac failure or anemia. Here, we discuss a case of a full-term neonate who was admitted to the neonatal care unit for birth asphyxia and neonatal sepsis and was consecutively diagnosed with HAVM and hypertrophic cardiomyopathy, along with persistent pulmonary hypertension.
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