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Prepancreatic postduodenal portal vein: a case report and literature review
BACKGROUND: Among congenital anomalies of the portal venous system, prepancreatic postduodenal portal vein (PPPV) is very rare and has only been reported to date. Herein, we report a case of PPPV identified in preoperative examinations for hepatocellular carcinoma and a literature review. CASE PRESE...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10123024/ https://www.ncbi.nlm.nih.gov/pubmed/37087704 http://dx.doi.org/10.1186/s40792-023-01644-5 |
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author | Akashi, Masanori Miyazaki, Daiki Hashimoto, Kazuaki Fukutomi, Shogo Arai, Shoichiro Goto, Yuichi Sato, Toshihiro Sakai, Hisamune Hisaka, Toru |
author_facet | Akashi, Masanori Miyazaki, Daiki Hashimoto, Kazuaki Fukutomi, Shogo Arai, Shoichiro Goto, Yuichi Sato, Toshihiro Sakai, Hisamune Hisaka, Toru |
author_sort | Akashi, Masanori |
collection | PubMed |
description | BACKGROUND: Among congenital anomalies of the portal venous system, prepancreatic postduodenal portal vein (PPPV) is very rare and has only been reported to date. Herein, we report a case of PPPV identified in preoperative examinations for hepatocellular carcinoma and a literature review. CASE PRESENTATION: A 63-year-old man was admitted to our hospital for treatment of a liver tumor. After examination, he was diagnosed with hepatocellular carcinoma with a diameter of 40 mm in segment 8. Contrast-enhanced computed tomography scan showed a portal vein passing between the duodenum and pancreas, hence called PPPV. At the hepatic hilus, the portal vein branched off in a complicated course with some porto-portal communications. We determined that anatomical resection with manipulation of the hepatic hilum in this case resulted in major vascular injury. Therefore, we performed partial liver resection, and the patient was discharged uneventfully on postoperative day 14. CONCLUSIONS: Although PPPV is an extremely rare congenital vascular variant, it is important to carefully identify vascular patterns preoperatively and to recognize the possibility of such an anomaly to avoid misidentification and inadvertent injuries during surgery. |
format | Online Article Text |
id | pubmed-10123024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-101230242023-04-25 Prepancreatic postduodenal portal vein: a case report and literature review Akashi, Masanori Miyazaki, Daiki Hashimoto, Kazuaki Fukutomi, Shogo Arai, Shoichiro Goto, Yuichi Sato, Toshihiro Sakai, Hisamune Hisaka, Toru Surg Case Rep Case Report BACKGROUND: Among congenital anomalies of the portal venous system, prepancreatic postduodenal portal vein (PPPV) is very rare and has only been reported to date. Herein, we report a case of PPPV identified in preoperative examinations for hepatocellular carcinoma and a literature review. CASE PRESENTATION: A 63-year-old man was admitted to our hospital for treatment of a liver tumor. After examination, he was diagnosed with hepatocellular carcinoma with a diameter of 40 mm in segment 8. Contrast-enhanced computed tomography scan showed a portal vein passing between the duodenum and pancreas, hence called PPPV. At the hepatic hilus, the portal vein branched off in a complicated course with some porto-portal communications. We determined that anatomical resection with manipulation of the hepatic hilum in this case resulted in major vascular injury. Therefore, we performed partial liver resection, and the patient was discharged uneventfully on postoperative day 14. CONCLUSIONS: Although PPPV is an extremely rare congenital vascular variant, it is important to carefully identify vascular patterns preoperatively and to recognize the possibility of such an anomaly to avoid misidentification and inadvertent injuries during surgery. Springer Berlin Heidelberg 2023-04-23 /pmc/articles/PMC10123024/ /pubmed/37087704 http://dx.doi.org/10.1186/s40792-023-01644-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Case Report Akashi, Masanori Miyazaki, Daiki Hashimoto, Kazuaki Fukutomi, Shogo Arai, Shoichiro Goto, Yuichi Sato, Toshihiro Sakai, Hisamune Hisaka, Toru Prepancreatic postduodenal portal vein: a case report and literature review |
title | Prepancreatic postduodenal portal vein: a case report and literature review |
title_full | Prepancreatic postduodenal portal vein: a case report and literature review |
title_fullStr | Prepancreatic postduodenal portal vein: a case report and literature review |
title_full_unstemmed | Prepancreatic postduodenal portal vein: a case report and literature review |
title_short | Prepancreatic postduodenal portal vein: a case report and literature review |
title_sort | prepancreatic postduodenal portal vein: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10123024/ https://www.ncbi.nlm.nih.gov/pubmed/37087704 http://dx.doi.org/10.1186/s40792-023-01644-5 |
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