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Multimodality imaging of Abernethy malformation

Abernethy malformation, or congenital extrahepatic portosystemic venous shunt, is a rare anomaly involving the portal venous system. Despite its rarity, it is increasingly being reported, and therefore, it is important to diagnose given the potential adverse clinical consequences if left untreated....

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Autores principales: El‐Medany, Ahmed Y., Rego, Gui, Williams, Matthew, Lyen, Stephen, Turner, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304201/
https://www.ncbi.nlm.nih.gov/pubmed/35170090
http://dx.doi.org/10.1111/echo.15324
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author El‐Medany, Ahmed Y.
Rego, Gui
Williams, Matthew
Lyen, Stephen
Turner, Mark
author_facet El‐Medany, Ahmed Y.
Rego, Gui
Williams, Matthew
Lyen, Stephen
Turner, Mark
author_sort El‐Medany, Ahmed Y.
collection PubMed
description Abernethy malformation, or congenital extrahepatic portosystemic venous shunt, is a rare anomaly involving the portal venous system. Despite its rarity, it is increasingly being reported, and therefore, it is important to diagnose given the potential adverse clinical consequences if left untreated. It has a spectrum of presentations, ranging from complete lack of symptoms, to causing hepatic carcinoma, hepatic encephalopathy, severe pulmonary hypertension, and diffuse pulmonary arteriovenous malformation. We herein describe the case and echocardiographic, computed tomography, and magnetic resonance imaging findings of a transgender individual, with this anomaly detected incidentally during adulthood.
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spelling pubmed-93042012022-07-28 Multimodality imaging of Abernethy malformation El‐Medany, Ahmed Y. Rego, Gui Williams, Matthew Lyen, Stephen Turner, Mark Echocardiography Case Reports Abernethy malformation, or congenital extrahepatic portosystemic venous shunt, is a rare anomaly involving the portal venous system. Despite its rarity, it is increasingly being reported, and therefore, it is important to diagnose given the potential adverse clinical consequences if left untreated. It has a spectrum of presentations, ranging from complete lack of symptoms, to causing hepatic carcinoma, hepatic encephalopathy, severe pulmonary hypertension, and diffuse pulmonary arteriovenous malformation. We herein describe the case and echocardiographic, computed tomography, and magnetic resonance imaging findings of a transgender individual, with this anomaly detected incidentally during adulthood. John Wiley and Sons Inc. 2022-02-16 2022-03 /pmc/articles/PMC9304201/ /pubmed/35170090 http://dx.doi.org/10.1111/echo.15324 Text en © 2022 The Authors. Echocardiography published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
El‐Medany, Ahmed Y.
Rego, Gui
Williams, Matthew
Lyen, Stephen
Turner, Mark
Multimodality imaging of Abernethy malformation
title Multimodality imaging of Abernethy malformation
title_full Multimodality imaging of Abernethy malformation
title_fullStr Multimodality imaging of Abernethy malformation
title_full_unstemmed Multimodality imaging of Abernethy malformation
title_short Multimodality imaging of Abernethy malformation
title_sort multimodality imaging of abernethy malformation
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304201/
https://www.ncbi.nlm.nih.gov/pubmed/35170090
http://dx.doi.org/10.1111/echo.15324
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