Pulmonary arterial hypertension combined with a high cardiac output state: Three remarkable cases
Identifieur interne : 005D18 ( Ncbi/Merge ); précédent : 005D17; suivant : 005D19Pulmonary arterial hypertension combined with a high cardiac output state: Three remarkable cases
Auteurs : Onno A. Spruijt [Pays-Bas] ; Harm-Jan Bogaard [Pays-Bas] ; Anton Vonk-Noordegraaf [Pays-Bas]Source :
- Pulmonary Circulation [ 2045-8932 ] ; 2013.
Abstract
A congenital extrahepatic portosystemic venous shunt (CEPVS), also known as an Abernethy malformation, is a rare cause of pulmonary arterial hypertension (PAH). In this case series, we describe three male patients of 30, 23, and 27 years of age with PAH due to a CEPVS. In all three patients, a right heart catheterization revealed a high cardiac output. The aim of this case series is to make pulmonary hypertension physicians aware of the possibility of a CEPVS when PAH is accompanied with a high cardiac output state.
Url:
DOI: 10.4103/2045-8932.113185
PubMed: 24015348
PubMed Central: 3757842
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<front><div type="abstract" xml:lang="en"><p>A congenital extrahepatic portosystemic venous shunt (CEPVS), also known as an Abernethy malformation, is a rare cause of pulmonary arterial hypertension (PAH). In this case series, we describe three male patients of 30, 23, and 27 years of age with PAH due to a CEPVS. In all three patients, a right heart catheterization revealed a high cardiac output. The aim of this case series is to make pulmonary hypertension physicians aware of the possibility of a CEPVS when PAH is accompanied with a high cardiac output state.</p>
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<front><journal-meta><journal-id journal-id-type="nlm-ta">Pulm Circ</journal-id>
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<title-group><article-title>Pulmonary arterial hypertension combined with a high cardiac output state: Three remarkable cases</article-title>
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<contrib-group><contrib contrib-type="author"><name><surname>Spruijt</surname>
<given-names>Onno A.</given-names>
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<contrib contrib-type="author"><name><surname>Bogaard</surname>
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<contrib contrib-type="author"><name><surname>Vonk-Noordegraaf</surname>
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<aff id="aff1">Department of Pulmonary Diseases, VU University Medical Center, Amsterdam, The Netherlands</aff>
<author-notes><corresp id="cor1"><bold>Address for correspondence: Prof. Anton Vonk-Noordegraaf</bold>
, VU University Medical Center, ZH-4A-48, 1000 SN Amsterdam, The Netherlands E-mail: <email xlink:href="A.Vonk@vumc.nl">A.Vonk@vumc.nl</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub"><season>Apr-Jun</season>
<year>2013</year>
</pub-date>
<volume>3</volume>
<issue>2</issue>
<fpage>440</fpage>
<lpage>443</lpage>
<permissions><copyright-statement>Copyright: © Pulmonary Circulation</copyright-statement>
<copyright-year>2013</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc-sa/3.0"><license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<abstract><p>A congenital extrahepatic portosystemic venous shunt (CEPVS), also known as an Abernethy malformation, is a rare cause of pulmonary arterial hypertension (PAH). In this case series, we describe three male patients of 30, 23, and 27 years of age with PAH due to a CEPVS. In all three patients, a right heart catheterization revealed a high cardiac output. The aim of this case series is to make pulmonary hypertension physicians aware of the possibility of a CEPVS when PAH is accompanied with a high cardiac output state.</p>
</abstract>
<kwd-group><kwd>abernethy malformation</kwd>
<kwd>congenital extrahepatic portosystemic venous shunt</kwd>
<kwd>congenital extrahepatic portosystemic shunt</kwd>
<kwd>pulmonary arterial hypertension</kwd>
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