Neonatal biliary atresia combined with preduodenal portal vein: A case report
| Autor: | Rui-Yun Zhang, Zhenwei Zhu, Qi Wang, Jun-Gang Zhao, Xian-Lan Xiang, Zhicheng Gu, Jianlei Chen, Hao-Wei Zhao, Jie Zhu, Peng Cai, Yu-Liang Jiang, Meng-Lei Zhu |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: |
medicine.medical_specialty
Cirrhosis business.industry medicine.medical_treatment Portal vein General Medicine Anastomosis Liver transplantation medicine.disease Surgery Treatment medicine.anatomical_structure Biliary atresia Neonatal Case report medicine Duodenum Cardiovascular malformations business Preduodenal portal vein Congenital biliary atresia |
| Zdroj: | World Journal of Clinical Cases |
| ISSN: | 2307-8960 |
| Popis: | Background Congenital biliary atresia is a type of obstruction of the bile ducts inside and outside the liver, which can lead to cholestatic liver cirrhosis and eventually liver failure. The preduodenal portal vein (PD-PV) is a rare developmental malformation of the PV. The PV courses in front of the duodenum. However, very few cases of neonatal biliary atresia combined with PD-PV have been reported in the scientific literature. Case summary A 1-mo-and-4-d-old child was admitted to the hospital in January because of yellowish skin. After surgical consultation, surgical intervention was recommended. The child underwent Hilar-jejunal anastomosis, duodenal rhomboid anastomosis, and abdominal drainage under general anesthesia. During the operation, the PV was located at the anterior edge of the duodenum. Conclusion Diagnoses: (1) Congenital biliary atresia; (2) PD-PV; and (3) Congenital cardiovascular malformations. Outcomes: Recommendation for liver transplantation. Lessons: The choice of treatment options for neonatal biliary atresia combined with PD-PV. |
| Databáze: | OpenAIRE |
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