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Hypoxia due to intrapulmonary vascular dilatation in a toddler with a congenital portacaval shunt: case report

BACKGROUND: The term hepatopulmonary syndrome typically applies to cyanosis that results from “intrapulmonary vascular dilatation” due to advanced liver disease. Similar findings may result from a congenital portosystemic shunt without liver disease. An adverse consequence of such shunts is intrapul...

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Detalles Bibliográficos
Autores principales: Alsamri, Mohammed T., Hamdan, Mohamed A., Sulaiman, Mohamed, Narchi, Hassib, Souid, Abdul-Kader
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387555/
https://www.ncbi.nlm.nih.gov/pubmed/30795758
http://dx.doi.org/10.1186/s12890-019-0788-8
Descripción
Sumario:BACKGROUND: The term hepatopulmonary syndrome typically applies to cyanosis that results from “intrapulmonary vascular dilatation” due to advanced liver disease. Similar findings may result from a congenital portosystemic shunt without liver disease. An adverse consequence of such shunts is intrapulmonary vascular dilatation, which affects the microvascular gas exchange units for oxygen. CASE PRESENTATION: Here, we describe a toddler with chronic cyanosis, exercise intolerance, and finger clubbing due to a malformation shunt between the portal vein and the inferior vena cava. A transcatheter embolization of the shunt resulted in resolution of his findings. CONCLUSIONS: Congenital portosystemic shunts need to be considered in the differential diagnosis of cyanosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12890-019-0788-8) contains supplementary material, which is available to authorized users.