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 ◽  
...  
2013 ◽  
Vol 76 (2) ◽  
pp. 137-142 ◽  
Author(s):  
Latha G. A. ◽  
Nagaraj A. Kagali ◽  
Shridhar M. ◽  
B. S. Satish Prasad

1990 ◽  
Vol 7 (1) ◽  
pp. 211
Author(s):  
Jae Hwang Kim ◽  
Young Soo Huh ◽  
Bo Yang Suh ◽  
Koing Bo Kwun

1994 ◽  
Vol 9 (5-6) ◽  
pp. 342-346 ◽  
Author(s):  
Toshio Chiba ◽  
Yoshie Hashida ◽  
Akira Takagi ◽  
Eduardo Yunis ◽  
David A. Lloyd ◽  
...  

Acta Medica ◽  
2019 ◽  
Vol 50 (4) ◽  
pp. 36-41
Author(s):  
Onder Ozden ◽  
Seref Selcuk Kılıc ◽  
Murat Alkan ◽  
Gokhan Tumgor ◽  
Recep Tuncer

Abstract: Introduction: The cause of biliary atresia (BA) is not understood exactly as well as biliary atresia splenic malformation (BASM) syndrome. BA is destructive biliary fibrosis; the etiology may be multifactorial. Association of cytomegalovirus (CMV) and BA have been shown in many reports but CMV and BASM have not been mentioned in the literature. So we aimed to report BASM experiences, an association of CMV infection and need of duodenoduodenostomy if preduodenal portal vein exists. Materials and Methods:  The data were collected retrospectively from Cukurova University which is one of the largest tertiary hospitals in Turkey between 2005-2017. The patients of sex, age, blood chemistry counts, TORCH infections blood parameters, BA types, operational findings and mortality were noted. Results: In total, 59 BA patients were diagnosed between 2005- 2017. Seven of them were classified as BASM.  The median age of them was 60 days (45-90 days). Three of them were girl and 4 of them were male in gender. The main complaint of whole patients was jaundice. The jaundice of 6 patients began since birth. One of them began at 20 days-age. Median total / direct blood bilirubin levels were 9.6 / 5.4 mg/dl. Median values of liver function tests; ALT, AST and GGT were 77 IU/L, 201 IU/L and 607 IU/L respectively. Five of the patients showed positive results for anti-CMV immunoglobulin M. All had positive anti-CMV Ig G and anti-toxoplasmosis Ig G. Evaluation of the types of BA revealed that one patient had type 2, while all others had type 3. Four of BASM patients had polysplenia and one had asplenia. Five of them had a preduodenal portal vein. All of them had midgut malrotation. One had inferior vena cava interruption. One had hepatic artery anomaly which was originated from SMA. The median time of follow-up was 4 years (1-5 years). All of them are alive and 1 required liver transplantation. Conclusion: BASM should be kept in mind by the surgeon for the requirement of additional surgical procedures such as Ladd procedure, duodenoduodenostomy with Kasai Porto-enterostomy. Duodenoduodenostomy may be performed when the existence of preduodenal portal vein. Further research is recommended for CMV infection and BASM.


2020 ◽  
Vol 9 ◽  
pp. 19
Author(s):  
Priyanka Mittal ◽  
Nitin James Peters ◽  
Ram Samujh

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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