z-logo
open-access-imgOpen Access
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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here