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Catastrophic intraoperative bleeding due to congenital extrahepatic porto-systemic shunt anomaly: A surgical case report of two rare anomalies
INTRODUCTION: Abernethy malformations are extremely rare congenital anomalous portosystemic shunts. We report the case of a patient with a rare variant Abernethy malformation between the superior mesenteric vein and left renal vein, associated with a massive jejunal diverticulum. PRESENTATION OF CAS...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928286/ https://www.ncbi.nlm.nih.gov/pubmed/29518666 http://dx.doi.org/10.1016/j.ijscr.2018.02.034 |
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author | Mohtashami, Ali Kiat, Andrew Cross, Jane Simon, Robert Curtin, Austin |
author_facet | Mohtashami, Ali Kiat, Andrew Cross, Jane Simon, Robert Curtin, Austin |
author_sort | Mohtashami, Ali |
collection | PubMed |
description | INTRODUCTION: Abernethy malformations are extremely rare congenital anomalous portosystemic shunts. We report the case of a patient with a rare variant Abernethy malformation between the superior mesenteric vein and left renal vein, associated with a massive jejunal diverticulum. PRESENTATION OF CASE: A 37-year-old Caucasian female presented to our emergency department with severe abdominal pain and proceeded to laparotomy for a presumed small bowel obstruction. At laparotomy she was found to have a massive diverticulum at the duodeno-jejunal junction, which was intimately associated with a venous malformation and the anomalous portosystemic shunt. Whilst mobilising the diverticulum, the patient developed catastrophic haemorrhage from the malformation. The patient underwent a complicated post-operative course however was eventually stabilised. DISCUSSION: We discuss the anatomy and pathophysiology of anomalous portosystemic shunts and propose an embryological origin for our patients’ anomalies. CONCLUSION: Abernethy malformations are rare however may be associated with other intra-abdominal pathology and extreme caution is required when operating on these patients. |
format | Online Article Text |
id | pubmed-5928286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-59282862018-05-03 Catastrophic intraoperative bleeding due to congenital extrahepatic porto-systemic shunt anomaly: A surgical case report of two rare anomalies Mohtashami, Ali Kiat, Andrew Cross, Jane Simon, Robert Curtin, Austin Int J Surg Case Rep Article INTRODUCTION: Abernethy malformations are extremely rare congenital anomalous portosystemic shunts. We report the case of a patient with a rare variant Abernethy malformation between the superior mesenteric vein and left renal vein, associated with a massive jejunal diverticulum. PRESENTATION OF CASE: A 37-year-old Caucasian female presented to our emergency department with severe abdominal pain and proceeded to laparotomy for a presumed small bowel obstruction. At laparotomy she was found to have a massive diverticulum at the duodeno-jejunal junction, which was intimately associated with a venous malformation and the anomalous portosystemic shunt. Whilst mobilising the diverticulum, the patient developed catastrophic haemorrhage from the malformation. The patient underwent a complicated post-operative course however was eventually stabilised. DISCUSSION: We discuss the anatomy and pathophysiology of anomalous portosystemic shunts and propose an embryological origin for our patients’ anomalies. CONCLUSION: Abernethy malformations are rare however may be associated with other intra-abdominal pathology and extreme caution is required when operating on these patients. Elsevier 2018-02-27 /pmc/articles/PMC5928286/ /pubmed/29518666 http://dx.doi.org/10.1016/j.ijscr.2018.02.034 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Mohtashami, Ali Kiat, Andrew Cross, Jane Simon, Robert Curtin, Austin Catastrophic intraoperative bleeding due to congenital extrahepatic porto-systemic shunt anomaly: A surgical case report of two rare anomalies |
title | Catastrophic intraoperative bleeding due to congenital extrahepatic porto-systemic shunt anomaly: A surgical case report of two rare anomalies |
title_full | Catastrophic intraoperative bleeding due to congenital extrahepatic porto-systemic shunt anomaly: A surgical case report of two rare anomalies |
title_fullStr | Catastrophic intraoperative bleeding due to congenital extrahepatic porto-systemic shunt anomaly: A surgical case report of two rare anomalies |
title_full_unstemmed | Catastrophic intraoperative bleeding due to congenital extrahepatic porto-systemic shunt anomaly: A surgical case report of two rare anomalies |
title_short | Catastrophic intraoperative bleeding due to congenital extrahepatic porto-systemic shunt anomaly: A surgical case report of two rare anomalies |
title_sort | catastrophic intraoperative bleeding due to congenital extrahepatic porto-systemic shunt anomaly: a surgical case report of two rare anomalies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928286/ https://www.ncbi.nlm.nih.gov/pubmed/29518666 http://dx.doi.org/10.1016/j.ijscr.2018.02.034 |
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