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Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer

RATIONALE: Heterotaxy with polysplenia is an extremely rare congenital condition resulting from abnormal arrangement of organs in the abdominal and thoracic cavities during embryologic development. When a malignancy such as pancreatic cancer develops under these conditions, surgical resection become...

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Autores principales: Pagkratis, Spyridon, Kryeziu, Sara, Lin, Miranda, Hoque, Samah, Bucobo, Juan Carlos, Buscaglia, Jonathan M., Georgakis, Georgios V., Sasson, Aaron R., Kim, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728835/
https://www.ncbi.nlm.nih.gov/pubmed/29245220
http://dx.doi.org/10.1097/MD.0000000000008599
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author Pagkratis, Spyridon
Kryeziu, Sara
Lin, Miranda
Hoque, Samah
Bucobo, Juan Carlos
Buscaglia, Jonathan M.
Georgakis, Georgios V.
Sasson, Aaron R.
Kim, Joseph
author_facet Pagkratis, Spyridon
Kryeziu, Sara
Lin, Miranda
Hoque, Samah
Bucobo, Juan Carlos
Buscaglia, Jonathan M.
Georgakis, Georgios V.
Sasson, Aaron R.
Kim, Joseph
author_sort Pagkratis, Spyridon
collection PubMed
description RATIONALE: Heterotaxy with polysplenia is an extremely rare congenital condition resulting from abnormal arrangement of organs in the abdominal and thoracic cavities during embryologic development. When a malignancy such as pancreatic cancer develops under these conditions, surgical resection becomes particularly complex. This case report demonstrates successful pancreatic cancer resection despite the patient's complicated anatomy. PATIENT CONCERNS: An 82-year-old female presented to our institution with complaints of mild right upper quadrant pain radiating to the mid-epigastric region. DIAGNOSES: Physical examination revealed jaundice with scleral icterus consistent with obstructive jaundice. Radiographic imaging revealed hepatic duct dilation with several anatomic anomalies including small bowel location in the right upper abdomen, cecum, and appendix in the left lower quadrant, reversed superior mesenteric artery and superior mesenteric vein positions, and right-sided duodenal-jejunal flexture as well as an entirely right-sided pancreas, and left lower pelvis with ≥6 separate splenules. These findings resulted in a diagnosis of heterotaxy syndrome with polysplenia. INTERVENTIONS: Careful preoperative planning and total pancreatectomy was performed without complication. OUTCOMES: The patient recovered well. Pathologic examination of the pancreatic mass revealed moderately/poorly differentiated invasive pancreatic duct adenocarcinoma. The patient remains alive and well without signs of recurrent disease at the 2-year follow-up. LESSONS: Given the wide range of anatomical variants observed in patients with heterotaxy syndrome, a thorough radiologic assessment is necessary before engaging in any surgical procedure. In our case, preoperative identification of the various anatomic anomalies, such as the short and vertically oriented pancreas, the porta hepatis position anterior to the duodenum, the nonrotation of the intestines and the anomalous origin of the right hepatic artery allowed us to perform a safe and uncomplicated total pancreatectomy.
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spelling pubmed-57288352017-12-20 Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer Pagkratis, Spyridon Kryeziu, Sara Lin, Miranda Hoque, Samah Bucobo, Juan Carlos Buscaglia, Jonathan M. Georgakis, Georgios V. Sasson, Aaron R. Kim, Joseph Medicine (Baltimore) 5700 RATIONALE: Heterotaxy with polysplenia is an extremely rare congenital condition resulting from abnormal arrangement of organs in the abdominal and thoracic cavities during embryologic development. When a malignancy such as pancreatic cancer develops under these conditions, surgical resection becomes particularly complex. This case report demonstrates successful pancreatic cancer resection despite the patient's complicated anatomy. PATIENT CONCERNS: An 82-year-old female presented to our institution with complaints of mild right upper quadrant pain radiating to the mid-epigastric region. DIAGNOSES: Physical examination revealed jaundice with scleral icterus consistent with obstructive jaundice. Radiographic imaging revealed hepatic duct dilation with several anatomic anomalies including small bowel location in the right upper abdomen, cecum, and appendix in the left lower quadrant, reversed superior mesenteric artery and superior mesenteric vein positions, and right-sided duodenal-jejunal flexture as well as an entirely right-sided pancreas, and left lower pelvis with ≥6 separate splenules. These findings resulted in a diagnosis of heterotaxy syndrome with polysplenia. INTERVENTIONS: Careful preoperative planning and total pancreatectomy was performed without complication. OUTCOMES: The patient recovered well. Pathologic examination of the pancreatic mass revealed moderately/poorly differentiated invasive pancreatic duct adenocarcinoma. The patient remains alive and well without signs of recurrent disease at the 2-year follow-up. LESSONS: Given the wide range of anatomical variants observed in patients with heterotaxy syndrome, a thorough radiologic assessment is necessary before engaging in any surgical procedure. In our case, preoperative identification of the various anatomic anomalies, such as the short and vertically oriented pancreas, the porta hepatis position anterior to the duodenum, the nonrotation of the intestines and the anomalous origin of the right hepatic artery allowed us to perform a safe and uncomplicated total pancreatectomy. Wolters Kluwer Health 2017-12-08 /pmc/articles/PMC5728835/ /pubmed/29245220 http://dx.doi.org/10.1097/MD.0000000000008599 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0
spellingShingle 5700
Pagkratis, Spyridon
Kryeziu, Sara
Lin, Miranda
Hoque, Samah
Bucobo, Juan Carlos
Buscaglia, Jonathan M.
Georgakis, Georgios V.
Sasson, Aaron R.
Kim, Joseph
Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer
title Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer
title_full Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer
title_fullStr Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer
title_full_unstemmed Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer
title_short Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer
title_sort case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer
topic 5700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728835/
https://www.ncbi.nlm.nih.gov/pubmed/29245220
http://dx.doi.org/10.1097/MD.0000000000008599
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