
Hemangioma – A pointer to Abernethy syndrome?
Author(s) -
Shyam Sunder Kothari
Publication year - 2020
Publication title -
annals of pediatric cardiology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.292
H-Index - 19
eISSN - 0974-2069
pISSN - 0974-5149
DOI - 10.4103/apc.apc_91_20
Subject(s) - medicine , portosystemic shunt , hemangioma , radiology , portal hypertension , cirrhosis
Diffuse pulmonary arteriovenous malformations or pulmonary arterial hypertension (PAH) may result from congenital portosystemic venous shunts. Hemangioma as a physical sign of congenital portosystemic shunts (like Abernethy syndrome) has not been described. I report two children (one with severe cyanosis from pulmonary arteriovenous malformations and the other with severe PAH) with cutaneous hemangioma and Abernethy syndrome. Hemangioma may be a clinical pointer to portosystemic shunts even in the absence of obvious liver disease.