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Non-operative management of a rare diagnosis of splenic torsion in a child with a history of giant omphalocele: a case report and literature review
BACKGROUND: Splenic torsion is rare and as a result the appropriate management is unclear. While there has been a shift towards splenectomy and laparoscopic splenopexy, we present a successful case of non-operative management of splenic torsion in a patient with a history of a giant omphalocele. CAS...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973840/ https://www.ncbi.nlm.nih.gov/pubmed/24602190 http://dx.doi.org/10.1186/1754-9493-8-12 |
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author | Sheikh, Fariha Kim, Michael E Zamora, Irving J Olutoye, Oluyinka O |
author_facet | Sheikh, Fariha Kim, Michael E Zamora, Irving J Olutoye, Oluyinka O |
author_sort | Sheikh, Fariha |
collection | PubMed |
description | BACKGROUND: Splenic torsion is rare and as a result the appropriate management is unclear. While there has been a shift towards splenectomy and laparoscopic splenopexy, we present a successful case of non-operative management of splenic torsion in a patient with a history of a giant omphalocele. CASE PRESENTATION: A 3 year-old female presented with a three-day history of abdominal pain, fever and non-bloody emesis three and a half years after repair of her giant omphalocele. Abdominal radiographs and ultrasound demonstrated migration of the spleen and a subsequent computerized tomography scan confirmed splenic torsion and an infarcted spleen. Given her late presentation, she was successfully managed with observation, analgesia, immunization against capsulated organisms and daily penicillin prophylaxis with excellent outcome at 19 months follow-up. A review of the literature revealed that splenic torsion is rarely managed non-operatively. Rarer still is the occurrence of splenic torsion following a history of omphalocele. CONCLUSION: Although rare, splenic torsion should be considered in a child with a history of omphalocele presenting with abdominal pain. Non-operative management of an infarcted spleen can be a safe treatment option to avoid surgery in complex patients. |
format | Online Article Text |
id | pubmed-3973840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39738402014-04-04 Non-operative management of a rare diagnosis of splenic torsion in a child with a history of giant omphalocele: a case report and literature review Sheikh, Fariha Kim, Michael E Zamora, Irving J Olutoye, Oluyinka O Patient Saf Surg Case Report BACKGROUND: Splenic torsion is rare and as a result the appropriate management is unclear. While there has been a shift towards splenectomy and laparoscopic splenopexy, we present a successful case of non-operative management of splenic torsion in a patient with a history of a giant omphalocele. CASE PRESENTATION: A 3 year-old female presented with a three-day history of abdominal pain, fever and non-bloody emesis three and a half years after repair of her giant omphalocele. Abdominal radiographs and ultrasound demonstrated migration of the spleen and a subsequent computerized tomography scan confirmed splenic torsion and an infarcted spleen. Given her late presentation, she was successfully managed with observation, analgesia, immunization against capsulated organisms and daily penicillin prophylaxis with excellent outcome at 19 months follow-up. A review of the literature revealed that splenic torsion is rarely managed non-operatively. Rarer still is the occurrence of splenic torsion following a history of omphalocele. CONCLUSION: Although rare, splenic torsion should be considered in a child with a history of omphalocele presenting with abdominal pain. Non-operative management of an infarcted spleen can be a safe treatment option to avoid surgery in complex patients. BioMed Central 2014-03-07 /pmc/articles/PMC3973840/ /pubmed/24602190 http://dx.doi.org/10.1186/1754-9493-8-12 Text en Copyright © 2014 Sheikh et al.; 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 Sheikh, Fariha Kim, Michael E Zamora, Irving J Olutoye, Oluyinka O Non-operative management of a rare diagnosis of splenic torsion in a child with a history of giant omphalocele: a case report and literature review |
title | Non-operative management of a rare diagnosis of splenic torsion in a child with a history of giant omphalocele: a case report and literature review |
title_full | Non-operative management of a rare diagnosis of splenic torsion in a child with a history of giant omphalocele: a case report and literature review |
title_fullStr | Non-operative management of a rare diagnosis of splenic torsion in a child with a history of giant omphalocele: a case report and literature review |
title_full_unstemmed | Non-operative management of a rare diagnosis of splenic torsion in a child with a history of giant omphalocele: a case report and literature review |
title_short | Non-operative management of a rare diagnosis of splenic torsion in a child with a history of giant omphalocele: a case report and literature review |
title_sort | non-operative management of a rare diagnosis of splenic torsion in a child with a history of giant omphalocele: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973840/ https://www.ncbi.nlm.nih.gov/pubmed/24602190 http://dx.doi.org/10.1186/1754-9493-8-12 |
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