Congenital hepatic arteriovenous malformation: An unusual cause of neonatal persistent pulmonary hypertension

C. P. Alexander, B. G. Sood, M. V. Zilberman, C. Becker, M. P. Bedard

Research output: Contribution to journalArticle

11 Scopus citations

Abstract

Congenital hepatic arteriovenous malformations are rare anomalies, which typically present in infancy with congestive heart failure, anemia, and hepatomegaly. Morbidity and mortality is high if the condition is not recognized and treated promptly. Hepatic arteriovenous malformation associated with persistent pulmonary hypertension of the newborn has been reported in two cases in the literature. We report a neonate who was referred for management of persistent pulmonary hypertension and was subsequently diagnosed with a large hepatic arteriovenous malformation. He underwent coil embolization following which pulmonary hypertension resolved.

Original languageEnglish (US)
Pages (from-to)316-318
Number of pages3
JournalJournal of Perinatology
Volume26
Issue number5
DOIs
StatePublished - May 2006

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health
  • Obstetrics and Gynecology

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