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Pseudomyxoma extraperitonei occurring 35 years after appendicectomy: a case report and review of literature
BACKGROUND: Pseudomyxoma peritonei is a rare condition consisting of mucinous ascites, most commonly arising from mucinous tumors of the appendix and occasionally from the ovary. Very rarely mucinous implants arise in the retroperitoneum without any intra-peritoneal involvement. This has been termed...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC436065/ https://www.ncbi.nlm.nih.gov/pubmed/15180896 http://dx.doi.org/10.1186/1477-7819-2-19 |
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author | Solkar, Mamoon H Akhtar, Naveed M Khan, Zareen Parker, Michael C |
author_facet | Solkar, Mamoon H Akhtar, Naveed M Khan, Zareen Parker, Michael C |
author_sort | Solkar, Mamoon H |
collection | PubMed |
description | BACKGROUND: Pseudomyxoma peritonei is a rare condition consisting of mucinous ascites, most commonly arising from mucinous tumors of the appendix and occasionally from the ovary. Very rarely mucinous implants arise in the retroperitoneum without any intra-peritoneal involvement. This has been termed as pseudomyxoma extraperitonei. CASE PRESENTATION: We report a case of a 57 year old man who developed pseudomyxoma extraperitonei, 35 years after undergoing an appendicectomy for a perforated appendix. CONCLUSIONS: Pseudomyxoma extraperitonei has been previously reported, however we report the longest incubation period of 35 years for this condition. |
format | Text |
id | pubmed-436065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-4360652004-06-26 Pseudomyxoma extraperitonei occurring 35 years after appendicectomy: a case report and review of literature Solkar, Mamoon H Akhtar, Naveed M Khan, Zareen Parker, Michael C World J Surg Oncol Case Report BACKGROUND: Pseudomyxoma peritonei is a rare condition consisting of mucinous ascites, most commonly arising from mucinous tumors of the appendix and occasionally from the ovary. Very rarely mucinous implants arise in the retroperitoneum without any intra-peritoneal involvement. This has been termed as pseudomyxoma extraperitonei. CASE PRESENTATION: We report a case of a 57 year old man who developed pseudomyxoma extraperitonei, 35 years after undergoing an appendicectomy for a perforated appendix. CONCLUSIONS: Pseudomyxoma extraperitonei has been previously reported, however we report the longest incubation period of 35 years for this condition. BioMed Central 2004-06-04 /pmc/articles/PMC436065/ /pubmed/15180896 http://dx.doi.org/10.1186/1477-7819-2-19 Text en Copyright © 2004 Solkar et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Case Report Solkar, Mamoon H Akhtar, Naveed M Khan, Zareen Parker, Michael C Pseudomyxoma extraperitonei occurring 35 years after appendicectomy: a case report and review of literature |
title | Pseudomyxoma extraperitonei occurring 35 years after appendicectomy: a case report and review of literature |
title_full | Pseudomyxoma extraperitonei occurring 35 years after appendicectomy: a case report and review of literature |
title_fullStr | Pseudomyxoma extraperitonei occurring 35 years after appendicectomy: a case report and review of literature |
title_full_unstemmed | Pseudomyxoma extraperitonei occurring 35 years after appendicectomy: a case report and review of literature |
title_short | Pseudomyxoma extraperitonei occurring 35 years after appendicectomy: a case report and review of literature |
title_sort | pseudomyxoma extraperitonei occurring 35 years after appendicectomy: a case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC436065/ https://www.ncbi.nlm.nih.gov/pubmed/15180896 http://dx.doi.org/10.1186/1477-7819-2-19 |
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