Prenatally diagnosed portocaval shunt and postnatal outcome: a case report |
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Authors: | Nicky Manning Lawrence Impey David Lindsell Kokila Lakhoo |
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Institution: | 1. Department of Fetal Medicine, John Radcliffe Hospital, Oxford, UK;2. Department of Radiology, John Radcliffe Hospital, Oxford, UK;3. Department of Paediatric Surgery, John Radcliffe Hospital, Oxford, UK |
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Abstract: | Congenital absence of the portal vein (CAPV) is a rare anomaly in the form of a portocaval shunt, whereby the intestinal and splenic venous drainage bypasses the liver and drains directly into the systemic circulation. We report a case of CAPV diagnosed prenatally after the recognition of a dilated umbilical vein draining directly into a large inferior vena cava (IVC). The IVC then drained into the right atrium of a dilated, hyperdynamic heart. The ductus venosus could not be identified. Repeated postnatal scans showed a gradual disappearance of venous lakes in the region of the porta hepatis and a clear drainage of the splenic vein to the left renal vein and the superior mesenteric vein to the IVC. From birth up to twelve months follow-up there was no evidence of liver dysfunction, encephalopathy or liver lesions. Copyright © 2004 John Wiley & Sons, Ltd. |
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Keywords: | portal vein portocaval shunt encephalopathy |
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