Preduodenal portal vein, malrotation, and high jejunal atresia: a case report

2012 ◽  
Vol 47 (1) ◽  
pp. e27-e30 ◽  
Author(s):  
Maciej Baglaj ◽  
Sylwester Gerus
Keyword(s):  
Case Report ◽  
Portal Vein ◽  
Jejunal Atresia ◽  
Preduodenal Portal Vein

scholarly journals Preduodenal Portal Vein in Adult with Polysplenia Syndrome Revisited with a Case Report

2013 ◽  
Vol 76 (2) ◽  
pp. 137-142 ◽  
Author(s):  
Latha G. A. ◽  
Nagaraj A. Kagali ◽  
Shridhar M. ◽  
B. S. Satish Prasad
Keyword(s):  
Case Report ◽  
Portal Vein ◽  
Polysplenia Syndrome ◽  
Preduodenal Portal Vein

Preduodenal Portal Vein Associated with Duodenal Obstruction: A case report

1990 ◽  
Vol 7 (1) ◽  
pp. 211
Author(s):  
Jae Hwang Kim ◽  
Young Soo Huh ◽  
Bo Yang Suh ◽  
Koing Bo Kwun
Keyword(s):  
Case Report ◽  
Portal Vein ◽  
Duodenal Obstruction ◽  
Preduodenal Portal Vein

scholarly journals Neonatal biliary atresia combined with preduodenal portal vein: A case report

2021 ◽  
Vol 9 (25) ◽  
pp. 7542-7550
Author(s):  
Xian-Lan Xiang ◽  
Peng Cai ◽  
Jun-Gang Zhao ◽  
Hao-Wei Zhao ◽  
Yu-Liang Jiang ◽  
...  
Keyword(s):  
Case Report ◽  
Portal Vein ◽  
Biliary Atresia ◽  
Preduodenal Portal Vein

A fatal combination of duodenal atresia with preduodenal portal vein, malrotation, and hypoplastic left heart syndrome: A case report

2020 ◽  
Vol 9 ◽  
pp. 19
Author(s):  
Priyanka Mittal ◽  
Nitin James Peters ◽  
Ram Samujh
Keyword(s):  
Case Report ◽  
Portal Vein ◽  
Cardiac Disease ◽  
Duodenal Atresia ◽  
Left Heart ◽  
Hypoplastic Left Heart ◽  
Case Presentation ◽  
Cardiac Anomalies ◽  
Preduodenal Portal Vein ◽  
Left Heart Syndrome

Background: Duodenal atresia (DA) is often associated with anomalies that include annular pancreas, cardiac anomalies, intestinal malrotation, situs inversus, or splenic anomalies. Association of duodenal atresia with complex cardiac anomalies is scarcely reported in the literature. Case Presentation: A term neonate was diagnosed with duodenal atresia and found to have a preduodenal portal vein and malrotation. A gastro jejunostomy was added to the procedure, due to the pre duodenal portal vein. On post-operative day 4, the patient had sudden desaturation. The respiratory system was normal and there was no evidence of septicaemia. On the post-operative echocardiogram, the diagnosis of hypoplastic left heart was made and the patient eventually succumbed to his complex cardiac disease. Conclusion: This is a rare combination of multiple anomalies and we report the clinical and anatomical findings of this patient.

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