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Duodenal duplication cyst extending into the posterior mediastinum
INTRODUCTION: Duodenal duplication is a rare congenital malformation. Although more frequent in childhood, it is rarely observed in adulthood. Preoperative diagnosis can be difficult. PRESENTATION OF CASE: We report a case of 42 year-old woman with duodenal duplication cyst situated in the posterior...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429960/ https://www.ncbi.nlm.nih.gov/pubmed/25732523 http://dx.doi.org/10.1016/j.ijscr.2015.02.022 |
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author | Sefa, Tuzun Mikail, Cakir Anil, Savas Umit, Gur Gokcen, Gundogdu |
author_facet | Sefa, Tuzun Mikail, Cakir Anil, Savas Umit, Gur Gokcen, Gundogdu |
author_sort | Sefa, Tuzun |
collection | PubMed |
description | INTRODUCTION: Duodenal duplication is a rare congenital malformation. Although more frequent in childhood, it is rarely observed in adulthood. Preoperative diagnosis can be difficult. PRESENTATION OF CASE: We report a case of 42 year-old woman with duodenal duplication cyst situated in the posterior mediastinum, who was misdiagnosed even after a primary surgery. Detailed diagnostic workup and a second operation was done. DISCUSSION: This article discusses the incidence of duodenal duplications, their types and clinical presentations, the radiologic and diagnostic features with different therapeutic options. CONCLUSION: Duodenal and the other intestinal duplication cysts should be considered in the differential diagnosis of oral contrast enhanced intrathoracic lesions in thorocoabdominal computerised tomography imaging. |
format | Online Article Text |
id | pubmed-4429960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-44299602015-05-15 Duodenal duplication cyst extending into the posterior mediastinum Sefa, Tuzun Mikail, Cakir Anil, Savas Umit, Gur Gokcen, Gundogdu Int J Surg Case Rep Case Report INTRODUCTION: Duodenal duplication is a rare congenital malformation. Although more frequent in childhood, it is rarely observed in adulthood. Preoperative diagnosis can be difficult. PRESENTATION OF CASE: We report a case of 42 year-old woman with duodenal duplication cyst situated in the posterior mediastinum, who was misdiagnosed even after a primary surgery. Detailed diagnostic workup and a second operation was done. DISCUSSION: This article discusses the incidence of duodenal duplications, their types and clinical presentations, the radiologic and diagnostic features with different therapeutic options. CONCLUSION: Duodenal and the other intestinal duplication cysts should be considered in the differential diagnosis of oral contrast enhanced intrathoracic lesions in thorocoabdominal computerised tomography imaging. Elsevier 2015-02-18 /pmc/articles/PMC4429960/ /pubmed/25732523 http://dx.doi.org/10.1016/j.ijscr.2015.02.022 Text en © 2015 The Authors 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 | Case Report Sefa, Tuzun Mikail, Cakir Anil, Savas Umit, Gur Gokcen, Gundogdu Duodenal duplication cyst extending into the posterior mediastinum |
title | Duodenal duplication cyst extending into the posterior mediastinum |
title_full | Duodenal duplication cyst extending into the posterior mediastinum |
title_fullStr | Duodenal duplication cyst extending into the posterior mediastinum |
title_full_unstemmed | Duodenal duplication cyst extending into the posterior mediastinum |
title_short | Duodenal duplication cyst extending into the posterior mediastinum |
title_sort | duodenal duplication cyst extending into the posterior mediastinum |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429960/ https://www.ncbi.nlm.nih.gov/pubmed/25732523 http://dx.doi.org/10.1016/j.ijscr.2015.02.022 |
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