Please use this identifier to cite or link to this item: https://accedacris.ulpgc.es/handle/10553/43685
DC FieldValueLanguage
dc.contributor.authorMartínez Quintana, Efrénen_US
dc.contributor.authorRodríguez-González, Faynaen_US
dc.date.accessioned2018-11-21T17:03:59Z-
dc.date.available2018-11-21T17:03:59Z-
dc.date.issued2014en_US
dc.identifier.issn2067-2993en_US
dc.identifier.urihttps://accedacris.ulpgc.es/handle/10553/43685-
dc.description.abstractThe hepatopulmonary syndrome is a rare complication of different types of chronic hepatic diseases with associated portal venous hypertension, resulting in pulmonary vascular dilatation, predominantly in the lower lung fields, and leading to ventilation-perfusion mismatch, arterial hypoxemia and a poor prognosis. We present the case of 42-year-old male patient with an anomalous drainage of the right superior pulmonary vein into the azygos vein and a portal vein cavernomatosis with associated portal venous hypertension who presented severe oxygen desaturation, during exercise, in the context of a hepatopulmonary syndrome.en_US
dc.languageengen_US
dc.publisher2067-2993-
dc.relation.ispartofPneumologiaen_US
dc.sourcePneumologia (Bucharest, Romania) [ISSN 2067-2993], v. 63, p. 48-50en_US
dc.subject32 Ciencias médicasen_US
dc.titleParadoxical arterial hypoxemia in a left-to-right shunt congenital heart diseaseen_US
dc.typeinfo:eu-repo/semantics/articlees
dc.typeArticlees
dc.identifier.scopus84903772116-
dc.contributor.authorscopusid23485891800-
dc.contributor.authorscopusid24825586600-
dc.description.lastpage50-
dc.description.firstpage48-
dc.relation.volume63-
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.identifier.ulpgces
dc.description.sjr0,151
dc.description.sjrqQ3
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.fullNameMartínez Quintana, Efrén-
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