A rare cause of congenital portosystemic shunt: type 2 Abernethy malformation

• Autorzy: Taydas O. , Danisan G. , Ogul H. , Kantarci M.
• Języki publikacji: EN

Abstrakty

EN

The Abernethy malformation is characterised by congenital extrahepatic portosystemic shunts and is divided into two groups according to the type of anastomosis. In type 1, all portal venous blood is discharged into the inferior vena cava and there is no intrahepatic portal vein. In type 2, the portal vein is partially discharged to the inferior vena cava via side-by-side anastomoses. Imaging has an important role in the diagnosis and follow-up of this malformation. Magnetic resonance imaging should be preferred to demonstrate both vessel anatomy and associated anomalies. The aim of this study was to present a 17-year-old male patient and to discuss the imaging findings of Abernethy malformation. (Folia Morphol 2020; 79, 1: 172–175)

• Wydawca: -
• Czasopismo: Folia Morphologica
• Rocznik: 2020
• Tom: 79
• Numer: 1
• Opis fizyczny: p.172-175,fig.,ref.

Twórcy

autor

Taydas O.

• Department of Radiology, Erzincan Binali Yildirim University Mengucek Gazi Training and Research Hospital, Erzincan, Turkey

autor

Danisan G.

• Mus State Hospital, Mus, Turkey

autor

Ogul H.

• Department of Radiology, Medical Faculty, Ataturk University, Erzurum, Turkey

autor

Kantarci M.

• Department of Radiology, Medical Faculty, Ataturk University, Erzurum, Turkey

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Identyfikatory

DOI

10.5603/FM.a2019.0063