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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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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. |
format | Online Article Text |
id | pubmed-8822688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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