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Small bowel infarction due to fibro muscular dysplasia: a case report and literature review
INTRODUCTION: We describe a rare case of small bowel infarction due to fibro muscular dysplasia in superior mesenteric artery in a young patient. CASE PRESENTATION: A 28 year old Asian female presented with acute onset left sided abdominal pain and watery diarrhea. She had a laparotomy due to furthe...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2862020/ https://www.ncbi.nlm.nih.gov/pubmed/20370894 http://dx.doi.org/10.1186/1757-1626-3-79 |
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author | Dalmia, Sanjay Hussain, Amir |
author_facet | Dalmia, Sanjay Hussain, Amir |
author_sort | Dalmia, Sanjay |
collection | PubMed |
description | INTRODUCTION: We describe a rare case of small bowel infarction due to fibro muscular dysplasia in superior mesenteric artery in a young patient. CASE PRESENTATION: A 28 year old Asian female presented with acute onset left sided abdominal pain and watery diarrhea. She had a laparotomy due to further deterioration. It showed infracted small intestine, gall bladder and parts of liver. Abdomen had to be closed without any therapeutic procedure. She died in early post operative period. Autopsy showed fibro muscular dysplasia of superior mesenteric artery. CONCLUSION: Fibro muscular dysplasia of SMA is rare, is treatable but has a high mortality. |
format | Text |
id | pubmed-2862020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28620202010-05-01 Small bowel infarction due to fibro muscular dysplasia: a case report and literature review Dalmia, Sanjay Hussain, Amir Cases J Case Report INTRODUCTION: We describe a rare case of small bowel infarction due to fibro muscular dysplasia in superior mesenteric artery in a young patient. CASE PRESENTATION: A 28 year old Asian female presented with acute onset left sided abdominal pain and watery diarrhea. She had a laparotomy due to further deterioration. It showed infracted small intestine, gall bladder and parts of liver. Abdomen had to be closed without any therapeutic procedure. She died in early post operative period. Autopsy showed fibro muscular dysplasia of superior mesenteric artery. CONCLUSION: Fibro muscular dysplasia of SMA is rare, is treatable but has a high mortality. BioMed Central 2010-04-06 /pmc/articles/PMC2862020/ /pubmed/20370894 http://dx.doi.org/10.1186/1757-1626-3-79 Text en Copyright ©2010 Dalmia and Hussain; 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 cited. |
spellingShingle | Case Report Dalmia, Sanjay Hussain, Amir Small bowel infarction due to fibro muscular dysplasia: a case report and literature review |
title | Small bowel infarction due to fibro muscular dysplasia: a case report and literature review |
title_full | Small bowel infarction due to fibro muscular dysplasia: a case report and literature review |
title_fullStr | Small bowel infarction due to fibro muscular dysplasia: a case report and literature review |
title_full_unstemmed | Small bowel infarction due to fibro muscular dysplasia: a case report and literature review |
title_short | Small bowel infarction due to fibro muscular dysplasia: a case report and literature review |
title_sort | small bowel infarction due to fibro muscular dysplasia: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2862020/ https://www.ncbi.nlm.nih.gov/pubmed/20370894 http://dx.doi.org/10.1186/1757-1626-3-79 |
work_keys_str_mv | AT dalmiasanjay smallbowelinfarctionduetofibromusculardysplasiaacasereportandliteraturereview AT hussainamir smallbowelinfarctionduetofibromusculardysplasiaacasereportandliteraturereview |