Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer
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 particula...
Gespeichert in:
Veröffentlicht in: | Medicine (Baltimore) 2017-12, Vol.96 (49), p.e8599-e8599 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | e8599 |
---|---|
container_issue | 49 |
container_start_page | e8599 |
container_title | Medicine (Baltimore) |
container_volume | 96 |
creator | Pagkratis, Spyridon Kryeziu, Sara Lin, Miranda Hoque, Samah Bucobo, Juan Carlos Buscaglia, Jonathan M. Georgakis, Georgios V. Sasson, Aaron R. Kim, Joseph |
description | 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.
An 82-year-old female presented to our institution with complaints of mild right upper quadrant pain radiating to the mid-epigastric region.
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.
Careful preoperative planning and total pancreatectomy was performed without complication.
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.
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. |
doi_str_mv | 10.1097/MD.0000000000008599 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5728835</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1977782287</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4509-5fe384b978e7219f1527e918364159549a2421b3f1bd016ecbdac86a49d060253</originalsourceid><addsrcrecordid>eNpdUVFvFCEQJkZjz-ovMDE8-tCtwMICLybmatWkjS_6TFh2trvKwQpcz_v35bzaVHmBmfm-j5n5EHpNyTklWr67vjgnj44SWj9BKyrarhG640_RihAmGqklP0Evcv5BCG0l48_RCdOMC8bICt2sbQacYImp4DjiORTIZQ7W4xBDk2KxZY7hDE9Q4BD93p9hGwa8RL_Pi4cw20rCFi8VCKHg3VymGgSXoGYcdvUJ6SV6Nlqf4dX9fYq-X378tv7cXH399GX94apxXBDdiBFaxXstFUhG9UgFk6CpajtOhRZcW8YZ7duR9gOhHbh-sE51luuBdHXa9hS9P-ou234Dg6sdJevNkuaNTXsT7Wz-rYR5Mjfx1gjJlGoPAm_vBVL8ta27MJs5O_DeBojbbKiWUirGlKzQ9gh1KeacYHz4hhJzsMhcX5j_LaqsN487fOD89aQC-BGwi77uPP_02x0kM4H1ZfqjJ6RmDSNUUkYUaQ4p3d4BWfmdBg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1977782287</pqid></control><display><type>article</type><title>Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Wolters Kluwer Open Health</source><source>IngentaConnect Free/Open Access Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Pagkratis, Spyridon ; Kryeziu, Sara ; Lin, Miranda ; Hoque, Samah ; Bucobo, Juan Carlos ; Buscaglia, Jonathan M. ; Georgakis, Georgios V. ; Sasson, Aaron R. ; Kim, Joseph</creator><creatorcontrib>Pagkratis, Spyridon ; Kryeziu, Sara ; Lin, Miranda ; Hoque, Samah ; Bucobo, Juan Carlos ; Buscaglia, Jonathan M. ; Georgakis, Georgios V. ; Sasson, Aaron R. ; Kim, Joseph</creatorcontrib><description>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.
An 82-year-old female presented to our institution with complaints of mild right upper quadrant pain radiating to the mid-epigastric region.
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.
Careful preoperative planning and total pancreatectomy was performed without complication.
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.
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.</description><identifier>ISSN: 0025-7974</identifier><identifier>EISSN: 1536-5964</identifier><identifier>DOI: 10.1097/MD.0000000000008599</identifier><identifier>PMID: 29245220</identifier><language>eng</language><publisher>United States: The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved</publisher><subject>Aged, 80 and over ; Clinical Case Report ; Female ; Heterotaxy Syndrome - complications ; Humans ; Intestinal Volvulus - complications ; Pancreas - surgery ; Pancreatectomy - methods ; Pancreatic Neoplasms - complications ; Pancreatic Neoplasms - surgery ; Spleen - abnormalities</subject><ispartof>Medicine (Baltimore), 2017-12, Vol.96 (49), p.e8599-e8599</ispartof><rights>The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved.</rights><rights>Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4509-5fe384b978e7219f1527e918364159549a2421b3f1bd016ecbdac86a49d060253</citedby><cites>FETCH-LOGICAL-c4509-5fe384b978e7219f1527e918364159549a2421b3f1bd016ecbdac86a49d060253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728835/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728835/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29245220$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pagkratis, Spyridon</creatorcontrib><creatorcontrib>Kryeziu, Sara</creatorcontrib><creatorcontrib>Lin, Miranda</creatorcontrib><creatorcontrib>Hoque, Samah</creatorcontrib><creatorcontrib>Bucobo, Juan Carlos</creatorcontrib><creatorcontrib>Buscaglia, Jonathan M.</creatorcontrib><creatorcontrib>Georgakis, Georgios V.</creatorcontrib><creatorcontrib>Sasson, Aaron R.</creatorcontrib><creatorcontrib>Kim, Joseph</creatorcontrib><title>Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer</title><title>Medicine (Baltimore)</title><addtitle>Medicine (Baltimore)</addtitle><description>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.
An 82-year-old female presented to our institution with complaints of mild right upper quadrant pain radiating to the mid-epigastric region.
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.
Careful preoperative planning and total pancreatectomy was performed without complication.
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.
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.</description><subject>Aged, 80 and over</subject><subject>Clinical Case Report</subject><subject>Female</subject><subject>Heterotaxy Syndrome - complications</subject><subject>Humans</subject><subject>Intestinal Volvulus - complications</subject><subject>Pancreas - surgery</subject><subject>Pancreatectomy - methods</subject><subject>Pancreatic Neoplasms - complications</subject><subject>Pancreatic Neoplasms - surgery</subject><subject>Spleen - abnormalities</subject><issn>0025-7974</issn><issn>1536-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdUVFvFCEQJkZjz-ovMDE8-tCtwMICLybmatWkjS_6TFh2trvKwQpcz_v35bzaVHmBmfm-j5n5EHpNyTklWr67vjgnj44SWj9BKyrarhG640_RihAmGqklP0Evcv5BCG0l48_RCdOMC8bICt2sbQacYImp4DjiORTIZQ7W4xBDk2KxZY7hDE9Q4BD93p9hGwa8RL_Pi4cw20rCFi8VCKHg3VymGgSXoGYcdvUJ6SV6Nlqf4dX9fYq-X378tv7cXH399GX94apxXBDdiBFaxXstFUhG9UgFk6CpajtOhRZcW8YZ7duR9gOhHbh-sE51luuBdHXa9hS9P-ou234Dg6sdJevNkuaNTXsT7Wz-rYR5Mjfx1gjJlGoPAm_vBVL8ta27MJs5O_DeBojbbKiWUirGlKzQ9gh1KeacYHz4hhJzsMhcX5j_LaqsN487fOD89aQC-BGwi77uPP_02x0kM4H1ZfqjJ6RmDSNUUkYUaQ4p3d4BWfmdBg</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Pagkratis, Spyridon</creator><creator>Kryeziu, Sara</creator><creator>Lin, Miranda</creator><creator>Hoque, Samah</creator><creator>Bucobo, Juan Carlos</creator><creator>Buscaglia, Jonathan M.</creator><creator>Georgakis, Georgios V.</creator><creator>Sasson, Aaron R.</creator><creator>Kim, Joseph</creator><general>The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved</general><general>Wolters Kluwer Health</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20171201</creationdate><title>Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer</title><author>Pagkratis, Spyridon ; Kryeziu, Sara ; Lin, Miranda ; Hoque, Samah ; Bucobo, Juan Carlos ; Buscaglia, Jonathan M. ; Georgakis, Georgios V. ; Sasson, Aaron R. ; Kim, Joseph</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4509-5fe384b978e7219f1527e918364159549a2421b3f1bd016ecbdac86a49d060253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged, 80 and over</topic><topic>Clinical Case Report</topic><topic>Female</topic><topic>Heterotaxy Syndrome - complications</topic><topic>Humans</topic><topic>Intestinal Volvulus - complications</topic><topic>Pancreas - surgery</topic><topic>Pancreatectomy - methods</topic><topic>Pancreatic Neoplasms - complications</topic><topic>Pancreatic Neoplasms - surgery</topic><topic>Spleen - abnormalities</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pagkratis, Spyridon</creatorcontrib><creatorcontrib>Kryeziu, Sara</creatorcontrib><creatorcontrib>Lin, Miranda</creatorcontrib><creatorcontrib>Hoque, Samah</creatorcontrib><creatorcontrib>Bucobo, Juan Carlos</creatorcontrib><creatorcontrib>Buscaglia, Jonathan M.</creatorcontrib><creatorcontrib>Georgakis, Georgios V.</creatorcontrib><creatorcontrib>Sasson, Aaron R.</creatorcontrib><creatorcontrib>Kim, Joseph</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medicine (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pagkratis, Spyridon</au><au>Kryeziu, Sara</au><au>Lin, Miranda</au><au>Hoque, Samah</au><au>Bucobo, Juan Carlos</au><au>Buscaglia, Jonathan M.</au><au>Georgakis, Georgios V.</au><au>Sasson, Aaron R.</au><au>Kim, Joseph</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer</atitle><jtitle>Medicine (Baltimore)</jtitle><addtitle>Medicine (Baltimore)</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>96</volume><issue>49</issue><spage>e8599</spage><epage>e8599</epage><pages>e8599-e8599</pages><issn>0025-7974</issn><eissn>1536-5964</eissn><abstract>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.
An 82-year-old female presented to our institution with complaints of mild right upper quadrant pain radiating to the mid-epigastric region.
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.
Careful preoperative planning and total pancreatectomy was performed without complication.
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.
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.</abstract><cop>United States</cop><pub>The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>29245220</pmid><doi>10.1097/MD.0000000000008599</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0025-7974 |
ispartof | Medicine (Baltimore), 2017-12, Vol.96 (49), p.e8599-e8599 |
issn | 0025-7974 1536-5964 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5728835 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Wolters Kluwer Open Health; IngentaConnect Free/Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection |
subjects | Aged, 80 and over Clinical Case Report Female Heterotaxy Syndrome - complications Humans Intestinal Volvulus - complications Pancreas - surgery Pancreatectomy - methods Pancreatic Neoplasms - complications Pancreatic Neoplasms - surgery Spleen - abnormalities |
title | Case report of intestinal non-rotation, heterotaxy, and polysplenia in a patient with pancreatic cancer |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T03%3A55%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Case%20report%20of%20intestinal%20non-rotation,%20heterotaxy,%20and%20polysplenia%20in%20a%20patient%20with%20pancreatic%20cancer&rft.jtitle=Medicine%20(Baltimore)&rft.au=Pagkratis,%20Spyridon&rft.date=2017-12-01&rft.volume=96&rft.issue=49&rft.spage=e8599&rft.epage=e8599&rft.pages=e8599-e8599&rft.issn=0025-7974&rft.eissn=1536-5964&rft_id=info:doi/10.1097/MD.0000000000008599&rft_dat=%3Cproquest_pubme%3E1977782287%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1977782287&rft_id=info:pmid/29245220&rfr_iscdi=true |