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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Case report : congenital extrahepatic portocaval shunt presenting as pulmonary arterial hypertension in a pregnant patient</dc:title><dc:creator>Harlander,	Matevž	(Avtor)
	</dc:creator><dc:creator>Badovinac,	Maja	(Avtor)
	</dc:creator><dc:creator>Markoska,	Frosina	(Avtor)
	</dc:creator><dc:creator>Salobir,	Barbara	(Avtor)
	</dc:creator><dc:creator>Štupnik,	Tomaž	(Avtor)
	</dc:creator><dc:creator>Dolenšek,	Marija	(Avtor)
	</dc:creator><dc:creator>Kern,	Izidor	(Avtor)
	</dc:creator><dc:creator>Gorjup,	Vojka	(Avtor)
	</dc:creator><dc:creator>Galiè,	Nazzareno	(Avtor)
	</dc:creator><dc:subject>pulmonary hypertension</dc:subject><dc:subject>pregnancy</dc:subject><dc:subject>congenital extrahepatic portocaval shunt</dc:subject><dc:subject>Abernethy malformation</dc:subject><dc:subject>pulmonary arterial hypertension</dc:subject><dc:description>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.</dc:description><dc:publisher>Wiley</dc:publisher><dc:date>2022</dc:date><dc:date>2022-01-10 13:26:06</dc:date><dc:type>Neznano</dc:type><dc:identifier>14709</dc:identifier><dc:identifier>UDK: 616.1</dc:identifier><dc:identifier>ISSN pri članku: 2045-8940</dc:identifier><dc:identifier>DOI: 10.1002/pul2.12008</dc:identifier><dc:identifier>COBISS_ID: 92131331</dc:identifier><dc:language>sl</dc:language><dc:rights>© 2021 The Authors</dc:rights></metadata>
