Congenital extrahepatic portocaval shunt (CEPS) is a rare condition in which a rare congenital vascular anomaly of the portal system is present. CEPS may manifest as pulmonary arterial hypertension (PAH). When diagnosed and treated early, PAH can be reversible. We report a case of a previously asymptomatic woman, who manifested with severe pulmonary hypertension during pregnancy and was consequently diagnosed with CEPS. After unsuccessful medical treatment, urgent lung transplantation was done.

Harlander M., Badovinac M., Markoska F., Salobir B., Stupnik T., Dolensek M.I., et al. (2022). Case report: Congenital extrahepatic portocaval shunt presenting as pulmonary arterial hypertension in a pregnant patient. PULMONARY CIRCULATION, 12(1), 1-4 [10.1002/pul2.12008].

Case report: Congenital extrahepatic portocaval shunt presenting as pulmonary arterial hypertension in a pregnant patient

Galie N.
2022

Abstract

Congenital extrahepatic portocaval shunt (CEPS) is a rare condition in which a rare congenital vascular anomaly of the portal system is present. CEPS may manifest as pulmonary arterial hypertension (PAH). When diagnosed and treated early, PAH can be reversible. We report a case of a previously asymptomatic woman, who manifested with severe pulmonary hypertension during pregnancy and was consequently diagnosed with CEPS. After unsuccessful medical treatment, urgent lung transplantation was done.
2022
Harlander M., Badovinac M., Markoska F., Salobir B., Stupnik T., Dolensek M.I., et al. (2022). Case report: Congenital extrahepatic portocaval shunt presenting as pulmonary arterial hypertension in a pregnant patient. PULMONARY CIRCULATION, 12(1), 1-4 [10.1002/pul2.12008].
Harlander M.; Badovinac M.; Markoska F.; Salobir B.; Stupnik T.; Dolensek M.I.; Kern I.; Gorjup V.; Galie N.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/903069
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