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A torted wandering spleen: a case report
INTRODUCTION: A torted wandering spleen is a rare clinical occurrence with fewer than 500 cases reported and an incidence of less than 0.2%. It is brought about through laxity of the gastrosplenic and splenorenal ligaments; however, the precise aetiology remains unknown. It can prove to be a diagnos...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4031896/ https://www.ncbi.nlm.nih.gov/pubmed/24886115 http://dx.doi.org/10.1186/1752-1947-8-133 |
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author | Sharma, Aman Salerno, Gisella |
author_facet | Sharma, Aman Salerno, Gisella |
author_sort | Sharma, Aman |
collection | PubMed |
description | INTRODUCTION: A torted wandering spleen is a rare clinical occurrence with fewer than 500 cases reported and an incidence of less than 0.2%. It is brought about through laxity of the gastrosplenic and splenorenal ligaments; however, the precise aetiology remains unknown. It can prove to be a diagnostic challenge with high mortality if misdiagnosed. CASE PRESENTATION: We present the case of a 27-year-old woman of Arabic ethnicity, who complained of a short history of severe abdominal pain with the background of recurrent abdominal pain and vomiting. An abdominal computerized tomography scan revealed a torted wandering spleen. This required a splenectomy due to splenic infarction. CONCLUSION: This report highlights the investigations and management necessary for a patient who presents with an ischaemic torted wandering spleen. |
format | Online Article Text |
id | pubmed-4031896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40318962014-05-24 A torted wandering spleen: a case report Sharma, Aman Salerno, Gisella J Med Case Rep Case Report INTRODUCTION: A torted wandering spleen is a rare clinical occurrence with fewer than 500 cases reported and an incidence of less than 0.2%. It is brought about through laxity of the gastrosplenic and splenorenal ligaments; however, the precise aetiology remains unknown. It can prove to be a diagnostic challenge with high mortality if misdiagnosed. CASE PRESENTATION: We present the case of a 27-year-old woman of Arabic ethnicity, who complained of a short history of severe abdominal pain with the background of recurrent abdominal pain and vomiting. An abdominal computerized tomography scan revealed a torted wandering spleen. This required a splenectomy due to splenic infarction. CONCLUSION: This report highlights the investigations and management necessary for a patient who presents with an ischaemic torted wandering spleen. BioMed Central 2014-05-01 /pmc/articles/PMC4031896/ /pubmed/24886115 http://dx.doi.org/10.1186/1752-1947-8-133 Text en Copyright © 2014 Sharma and Salerno; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Sharma, Aman Salerno, Gisella A torted wandering spleen: a case report |
title | A torted wandering spleen: a case report |
title_full | A torted wandering spleen: a case report |
title_fullStr | A torted wandering spleen: a case report |
title_full_unstemmed | A torted wandering spleen: a case report |
title_short | A torted wandering spleen: a case report |
title_sort | torted wandering spleen: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4031896/ https://www.ncbi.nlm.nih.gov/pubmed/24886115 http://dx.doi.org/10.1186/1752-1947-8-133 |
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