Abstract

Preduodenal portal vein (PDPV) is a rare congenital vascular anomaly in which the portal vein passesanterior to the duodenum rather than posteriorly. Generally asymptomatic, PDPV may rarely cause aduodenal obstruction in the newborn. It is usually associated with gastrointestinal tract, cardiac,pancreatic, as well as biliary tract anomalies or may, occur as a single isolated malformation. Tillnow, only a few cases have been reported with duodenal obstruction and associated anomalies. Thepresent study report one such case of PDPV with multiple congenital anomalies. A full-term, one-day-old baby who had an antenatal history of polyhydramnios, presented to us with abdominaldistension and non-bilious vomitings soon after birth. Surgical exploration revealed a hugely dilatedstomach, multiple Ladd bands, malrotation of the small intestine, preduodenal portal vein, and anannular pancreas causing external duodenal compression. Intraoperative recognition of PDPV isimportant because iatrogenic injury during surgery can cause profuse hemorrhage from the vein andmay cause damage to the biliary tract or duodenal wall. Prompt evaluation of associated cardiacanomalies is important before surgery. Duodenostomy anterior to the portal vein is the definitivetreatment. Studies in animal models (AKR/J mice) have shown an autosomal recessive mode ofinheritance.

Highlights

  • The present study report one such case of Preduodenal portal vein (PDPV) with multiple congenital anomalies

  • The preduodenal portal vein, which runs at the ventral side of the duodenum is a rare congenital anomaly in humans

  • The theory to account for the development of a preduodenal portal vein was put forth by His in 1885 [1], and an example of this anomaly in a pig embryo was reported by Begg in 1912 [2]

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Summary

Introduction

The preduodenal portal vein, which runs at the ventral side of the duodenum is a rare congenital anomaly in humans. Many cases have been reported in children and adults, as well as during surgery [4,5,6] It is found sporadically during investigations of epigastric pain or other symptoms, such as vomiting or jaundice. This anomaly has a high association with other congenital anomalies, such as malrotation; situs inversus; pancreatic, duodenal, biliary system, and splenic anomalies; as well as dextrocardia. Laparotomy was done which revealed a hugely dilated stomach, multiple Ladd bands, malrotation of the small intestine, a Preduodenal portal vein, and an annular pancreas causing external duodenal compression. Fig-2: Malrotation of the small intestine and annular pancreas

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