Spontaneous Resolution of Congenital Intrahepatic Portosystemic Shunt
- PMID: 40060247
- PMCID: PMC11887818
- DOI: 10.15388/Amed.2024.31.2.14
Spontaneous Resolution of Congenital Intrahepatic Portosystemic Shunt
Abstract
Congenital portosystemic shunts (CPSS) are a rare type of congenital abnormality. It results from abnormal embryonic development by the fourth week of fetal life. Congenital portosystemic shunts are believed to signify persistent communication between the portal and vitelline venous systems. Both extrahepatic and intrahepatic shunts are possible. They may develop on their own or in association with other congenital abnormalities. With regard to shunt type and size, symptoms vary widely. The anatomy of the shunt and associated abnormalities can be assessed by computed tomography and magnetic resonance angiography. The treatment plan is based on the type of shunt, its location and level of function, the patient's age, and the severity of their symptoms.
įgimtas portosisteminis šuntas (angl. Congenital portosystemic shunts, CPSS) yra reta įgimta anomalija. Ji atsiranda dėl netaisyklingo embriono vystymosi iki ketvirtos vaisiaus gyvenimo savaitės. Manoma, kad įgimti portosisteminiai šuntai reiškia nuolatinį portalinės ir stiklakūnio venų sistemos ryšį. Galimi tiek ekstrahepatiniai, tiek intrahepatiniai šuntai. Jie gali išsivystyti atskirai arba kartu su kitomis įgimtomis anomalijomis. Atsižvelgiant į šunto tipą ir dydį, simptomai labai skiriasi. Šunto anatomiją ir susijusias anomalijas galima įvertinti kompiuterinės tomografijos ir magnetinio rezonanso angiografijos metodais. Gydymo planas sudaromas atsižvelgiant į šunto tipą, jo vietą ir funkcijos lygį, paciento amžių ir simptomų sunkumą.
Keywords: Abernathy malformation; congenital portosystemic shunts; embolization.
Copyright © 2024 Taraprasad Tripathy, Sandeep Behera, Ranjan Patel, Tanmay Dutta, Aditi Kumar, Amit Kumar Satpathy. Published by Vilnius University Press.
Conflict of interest statement
None to declare
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References
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