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Idiopathic Adult Ileoileal and Ileocolic Intussusception in situs Inversus Totalis: A Rare Coincidence
Situs inversus totalis is a rare autosomal recessive congenital anomaly that is characterized by mirror image anatomy of the abdominal and thoracic organs. We report a case of a 28-year-old male with situs inversus totalis, who developed an idiopathic ileoileal and ileocolic intussusception, which w...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271699/ https://www.ncbi.nlm.nih.gov/pubmed/22249097 http://dx.doi.org/10.4103/1319-3767.91732 |
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author | Butt, Nazish Shah, Syed H. Alvi, Abdul R. Tanveer-ul-Haq, Hassan, Saba |
author_facet | Butt, Nazish Shah, Syed H. Alvi, Abdul R. Tanveer-ul-Haq, Hassan, Saba |
author_sort | Butt, Nazish |
collection | PubMed |
description | Situs inversus totalis is a rare autosomal recessive congenital anomaly that is characterized by mirror image anatomy of the abdominal and thoracic organs. We report a case of a 28-year-old male with situs inversus totalis, who developed an idiopathic ileoileal and ileocolic intussusception, which was diagnosed on computed tomography scan. Patient underwent successfully ileal resection and side-to-side functional anastomosis of ileum 12 cms from ileocecal junction. Postoperative course was uneventful. To the best of our knowledge, this is the first case of idiopathic adult intussusception with situs inversus totalis in the literature. |
format | Online Article Text |
id | pubmed-3271699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-32716992012-02-15 Idiopathic Adult Ileoileal and Ileocolic Intussusception in situs Inversus Totalis: A Rare Coincidence Butt, Nazish Shah, Syed H. Alvi, Abdul R. Tanveer-ul-Haq, Hassan, Saba Saudi J Gastroenterol Case Report Situs inversus totalis is a rare autosomal recessive congenital anomaly that is characterized by mirror image anatomy of the abdominal and thoracic organs. We report a case of a 28-year-old male with situs inversus totalis, who developed an idiopathic ileoileal and ileocolic intussusception, which was diagnosed on computed tomography scan. Patient underwent successfully ileal resection and side-to-side functional anastomosis of ileum 12 cms from ileocecal junction. Postoperative course was uneventful. To the best of our knowledge, this is the first case of idiopathic adult intussusception with situs inversus totalis in the literature. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3271699/ /pubmed/22249097 http://dx.doi.org/10.4103/1319-3767.91732 Text en Copyright: © Saudi Journal of Gastroenterology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Butt, Nazish Shah, Syed H. Alvi, Abdul R. Tanveer-ul-Haq, Hassan, Saba Idiopathic Adult Ileoileal and Ileocolic Intussusception in situs Inversus Totalis: A Rare Coincidence |
title | Idiopathic Adult Ileoileal and Ileocolic Intussusception in situs Inversus Totalis: A Rare Coincidence |
title_full | Idiopathic Adult Ileoileal and Ileocolic Intussusception in situs Inversus Totalis: A Rare Coincidence |
title_fullStr | Idiopathic Adult Ileoileal and Ileocolic Intussusception in situs Inversus Totalis: A Rare Coincidence |
title_full_unstemmed | Idiopathic Adult Ileoileal and Ileocolic Intussusception in situs Inversus Totalis: A Rare Coincidence |
title_short | Idiopathic Adult Ileoileal and Ileocolic Intussusception in situs Inversus Totalis: A Rare Coincidence |
title_sort | idiopathic adult ileoileal and ileocolic intussusception in situs inversus totalis: a rare coincidence |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271699/ https://www.ncbi.nlm.nih.gov/pubmed/22249097 http://dx.doi.org/10.4103/1319-3767.91732 |
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