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A new variant of Abernethy malformation treated by transhepatic interventional closure: a case report

BACKGROUND: Congenital portosystemic shunts (CPSS) are rare vascular malformations and can be classified into extrahepatic and intrahepatic shunts. Extrahepatic CPSS, also termed Abernethy malformations are associated with severe long-term complications including portopulmonary hypertension, liver a...

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Autores principales: Sieverding, Ludger, Hofbeck, Michael, Michel, Jörg, Hornung, Andreas, Scheckenbach, Christian, Grözinger, Gerd, Sturm, Ekkehard, Warmann, Steven W., Hanser, Anja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822688/
https://www.ncbi.nlm.nih.gov/pubmed/35130851
http://dx.doi.org/10.1186/s12876-022-02123-1
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author Sieverding, Ludger
Hofbeck, Michael
Michel, Jörg
Hornung, Andreas
Scheckenbach, Christian
Grözinger, Gerd
Sturm, Ekkehard
Warmann, Steven W.
Hanser, Anja
author_facet Sieverding, Ludger
Hofbeck, Michael
Michel, Jörg
Hornung, Andreas
Scheckenbach, Christian
Grözinger, Gerd
Sturm, Ekkehard
Warmann, Steven W.
Hanser, Anja
author_sort Sieverding, Ludger
collection PubMed
description BACKGROUND: Congenital portosystemic shunts (CPSS) are rare vascular malformations and can be classified into extrahepatic and intrahepatic shunts. Extrahepatic CPSS, also termed Abernethy malformations are associated with severe long-term complications including portopulmonary hypertension, liver atrophy, hyperammoniemia and hepatic encephalopathy. We report a hitherto undescribed variant of Abernethy malformation requiring an innovative approach for interventional treatment. CASE PRESENTATION: We describe a 31-year-old patient following surgical repair of atrioventricular septal defect at the age of 6 years. In the long-term follow-up he showed persistent pulmonary hypertension which deteriorated despite dual pulmonary vasodilative treatment. When he developed arterial desaturation and symptomatic hyperammoniemia detailed reassessment revealed as underlying cause a hitherto undescribed variant of Abernethy malformation connecting the portal vein with the right lower pulmonary vein. Following interdisciplinary discussions we opted for an interventional approach. Since the malformation was un-accessible to interventional closure via antegrade venous or retrograde arterial access, a transhepatic percutaneous puncture of the portal vein was performed. Temporary balloon occlusion of the malformation revealed only a slight increase in portal venous pressure. Interventional occlusion of the large vascular connection was achieved via this transhepatic approach by successive implantation of two large vascular occluding devices. The postinterventional course was unremarkable and both ammonia levels and arterial saturation normalized at follow-up of 12 months. CONCLUSIONS: Portal vein anomalies should be included in the differential diagnoses of pulmonary hypertension or pulmonary arterio-venous malformations. Based on careful assessment of the anatomy and testing of portal vein hemodynamics interventional therapy of complex Abernethy malformations can be performed successfully in specialized centers.
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spelling pubmed-88226882022-02-08 A new variant of Abernethy malformation treated by transhepatic interventional closure: a case report Sieverding, Ludger Hofbeck, Michael Michel, Jörg Hornung, Andreas Scheckenbach, Christian Grözinger, Gerd Sturm, Ekkehard Warmann, Steven W. Hanser, Anja BMC Gastroenterol Case Report BACKGROUND: Congenital portosystemic shunts (CPSS) are rare vascular malformations and can be classified into extrahepatic and intrahepatic shunts. Extrahepatic CPSS, also termed Abernethy malformations are associated with severe long-term complications including portopulmonary hypertension, liver atrophy, hyperammoniemia and hepatic encephalopathy. We report a hitherto undescribed variant of Abernethy malformation requiring an innovative approach for interventional treatment. CASE PRESENTATION: We describe a 31-year-old patient following surgical repair of atrioventricular septal defect at the age of 6 years. In the long-term follow-up he showed persistent pulmonary hypertension which deteriorated despite dual pulmonary vasodilative treatment. When he developed arterial desaturation and symptomatic hyperammoniemia detailed reassessment revealed as underlying cause a hitherto undescribed variant of Abernethy malformation connecting the portal vein with the right lower pulmonary vein. Following interdisciplinary discussions we opted for an interventional approach. Since the malformation was un-accessible to interventional closure via antegrade venous or retrograde arterial access, a transhepatic percutaneous puncture of the portal vein was performed. Temporary balloon occlusion of the malformation revealed only a slight increase in portal venous pressure. Interventional occlusion of the large vascular connection was achieved via this transhepatic approach by successive implantation of two large vascular occluding devices. The postinterventional course was unremarkable and both ammonia levels and arterial saturation normalized at follow-up of 12 months. CONCLUSIONS: Portal vein anomalies should be included in the differential diagnoses of pulmonary hypertension or pulmonary arterio-venous malformations. Based on careful assessment of the anatomy and testing of portal vein hemodynamics interventional therapy of complex Abernethy malformations can be performed successfully in specialized centers. BioMed Central 2022-02-07 /pmc/articles/PMC8822688/ /pubmed/35130851 http://dx.doi.org/10.1186/s12876-022-02123-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Sieverding, Ludger
Hofbeck, Michael
Michel, Jörg
Hornung, Andreas
Scheckenbach, Christian
Grözinger, Gerd
Sturm, Ekkehard
Warmann, Steven W.
Hanser, Anja
A new variant of Abernethy malformation treated by transhepatic interventional closure: a case report
title A new variant of Abernethy malformation treated by transhepatic interventional closure: a case report
title_full A new variant of Abernethy malformation treated by transhepatic interventional closure: a case report
title_fullStr A new variant of Abernethy malformation treated by transhepatic interventional closure: a case report
title_full_unstemmed A new variant of Abernethy malformation treated by transhepatic interventional closure: a case report
title_short A new variant of Abernethy malformation treated by transhepatic interventional closure: a case report
title_sort new variant of abernethy malformation treated by transhepatic interventional closure: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822688/
https://www.ncbi.nlm.nih.gov/pubmed/35130851
http://dx.doi.org/10.1186/s12876-022-02123-1
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