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An adolescent girl in Hong Kong with type Ib Abernethy malformation complicated by multiple focal nodular hyperplasia

Congenital portosystemic venous shunts are developmental anomalies. They represent portal communication with the systemic circulation. The pathogenesis is linked to the complexity of the embryological development of the inferior vena cava and portal vein. We reported a case of an asymptomatic 14-yea...

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Detalles Bibliográficos
Autores principales: Yam, Max Kai Ho, Cheung, Kin On, Sim, Shiu Wah, Lee, Paul Sing Fun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522042/
https://www.ncbi.nlm.nih.gov/pubmed/33014233
http://dx.doi.org/10.1016/j.radcr.2020.09.016
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author Yam, Max Kai Ho
Cheung, Kin On
Sim, Shiu Wah
Lee, Paul Sing Fun
author_facet Yam, Max Kai Ho
Cheung, Kin On
Sim, Shiu Wah
Lee, Paul Sing Fun
author_sort Yam, Max Kai Ho
collection PubMed
description Congenital portosystemic venous shunts are developmental anomalies. They represent portal communication with the systemic circulation. The pathogenesis is linked to the complexity of the embryological development of the inferior vena cava and portal vein. We reported a case of an asymptomatic 14-year-old Chinese adolescent girl in Hong Kong with a confirmed congenital portosystemic shunt type 1b. The condition can be diagnosed using contrast-enhanced CT scans and MRIs. Early recognition of the condition is important due to elevated risks of developing hepatocellular tumours. Liver transplantation may be considered curative.
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spelling pubmed-75220422020-10-02 An adolescent girl in Hong Kong with type Ib Abernethy malformation complicated by multiple focal nodular hyperplasia Yam, Max Kai Ho Cheung, Kin On Sim, Shiu Wah Lee, Paul Sing Fun Radiol Case Rep Case Report Congenital portosystemic venous shunts are developmental anomalies. They represent portal communication with the systemic circulation. The pathogenesis is linked to the complexity of the embryological development of the inferior vena cava and portal vein. We reported a case of an asymptomatic 14-year-old Chinese adolescent girl in Hong Kong with a confirmed congenital portosystemic shunt type 1b. The condition can be diagnosed using contrast-enhanced CT scans and MRIs. Early recognition of the condition is important due to elevated risks of developing hepatocellular tumours. Liver transplantation may be considered curative. Elsevier 2020-09-25 /pmc/articles/PMC7522042/ /pubmed/33014233 http://dx.doi.org/10.1016/j.radcr.2020.09.016 Text en © 2020 The Authors. Published by Elsevier Inc. on behalf of University of Washington. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Yam, Max Kai Ho
Cheung, Kin On
Sim, Shiu Wah
Lee, Paul Sing Fun
An adolescent girl in Hong Kong with type Ib Abernethy malformation complicated by multiple focal nodular hyperplasia
title An adolescent girl in Hong Kong with type Ib Abernethy malformation complicated by multiple focal nodular hyperplasia
title_full An adolescent girl in Hong Kong with type Ib Abernethy malformation complicated by multiple focal nodular hyperplasia
title_fullStr An adolescent girl in Hong Kong with type Ib Abernethy malformation complicated by multiple focal nodular hyperplasia
title_full_unstemmed An adolescent girl in Hong Kong with type Ib Abernethy malformation complicated by multiple focal nodular hyperplasia
title_short An adolescent girl in Hong Kong with type Ib Abernethy malformation complicated by multiple focal nodular hyperplasia
title_sort adolescent girl in hong kong with type ib abernethy malformation complicated by multiple focal nodular hyperplasia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522042/
https://www.ncbi.nlm.nih.gov/pubmed/33014233
http://dx.doi.org/10.1016/j.radcr.2020.09.016
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