Cargando…

Leiomyosarcoma of the small bowel: Report of a case and review of the literature

INTRODUCTION: Leiomyosarcoma of the small bowel is an extremely rare form of gastrointestinal malignancy. Small bowel tumours are usually asymptomatic at the early stages, and difficult to visualise by upper and lower endoscopy. PRESENTATION OF CASE: An 83-year-old gentleman presented in surgical ou...

Descripción completa

Detalles Bibliográficos
Autores principales: Luis, Joshua, Ejtehadi, Farshid, Howlett, David C., Donnellan, Imelda M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4334955/
https://www.ncbi.nlm.nih.gov/pubmed/25506852
http://dx.doi.org/10.1016/j.ijscr.2014.11.009
_version_ 1782358259502415872
author Luis, Joshua
Ejtehadi, Farshid
Howlett, David C.
Donnellan, Imelda M.
author_facet Luis, Joshua
Ejtehadi, Farshid
Howlett, David C.
Donnellan, Imelda M.
author_sort Luis, Joshua
collection PubMed
description INTRODUCTION: Leiomyosarcoma of the small bowel is an extremely rare form of gastrointestinal malignancy. Small bowel tumours are usually asymptomatic at the early stages, and difficult to visualise by upper and lower endoscopy. PRESENTATION OF CASE: An 83-year-old gentleman presented in surgical outpatient clinic with chronic anaemia, abdominal discomfort and a single episode of malaena. Initial OGD and colonoscopy were both unremarkable. Subsequent CT revealed a mass in the right iliac fossa of likely small bowel origin, leading to an urgent laparotomy and resection with primary anastomosis. Histopathology showed a high grade leiomyosarcoma with no signs of metastasis and confirmatory immunological staining. Post-surgery follow up remains unremarkable. DISCUSSION: Leiomyosarcomas of the small bowel are extremely rare entities, particularly following the advent of robust immunohistological diagnostic methods allowing differentiation from GISTs. As small bowel tumours are often not visualised by upper and lower endoscopy, further investigations to visualise the small bowel are crucial, generally in the form of magnetic resonance enterography, CT colonography or wireless capsule endoscopy. CONCLUSION: The treatment of such tumours remains predominantly centred around surgical resection, and prognosis is dependent on tumour size and histological staging.
format Online
Article
Text
id pubmed-4334955
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-43349552015-03-03 Leiomyosarcoma of the small bowel: Report of a case and review of the literature Luis, Joshua Ejtehadi, Farshid Howlett, David C. Donnellan, Imelda M. Int J Surg Case Rep Article INTRODUCTION: Leiomyosarcoma of the small bowel is an extremely rare form of gastrointestinal malignancy. Small bowel tumours are usually asymptomatic at the early stages, and difficult to visualise by upper and lower endoscopy. PRESENTATION OF CASE: An 83-year-old gentleman presented in surgical outpatient clinic with chronic anaemia, abdominal discomfort and a single episode of malaena. Initial OGD and colonoscopy were both unremarkable. Subsequent CT revealed a mass in the right iliac fossa of likely small bowel origin, leading to an urgent laparotomy and resection with primary anastomosis. Histopathology showed a high grade leiomyosarcoma with no signs of metastasis and confirmatory immunological staining. Post-surgery follow up remains unremarkable. DISCUSSION: Leiomyosarcomas of the small bowel are extremely rare entities, particularly following the advent of robust immunohistological diagnostic methods allowing differentiation from GISTs. As small bowel tumours are often not visualised by upper and lower endoscopy, further investigations to visualise the small bowel are crucial, generally in the form of magnetic resonance enterography, CT colonography or wireless capsule endoscopy. CONCLUSION: The treatment of such tumours remains predominantly centred around surgical resection, and prognosis is dependent on tumour size and histological staging. Elsevier 2014-11-11 /pmc/articles/PMC4334955/ /pubmed/25506852 http://dx.doi.org/10.1016/j.ijscr.2014.11.009 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Luis, Joshua
Ejtehadi, Farshid
Howlett, David C.
Donnellan, Imelda M.
Leiomyosarcoma of the small bowel: Report of a case and review of the literature
title Leiomyosarcoma of the small bowel: Report of a case and review of the literature
title_full Leiomyosarcoma of the small bowel: Report of a case and review of the literature
title_fullStr Leiomyosarcoma of the small bowel: Report of a case and review of the literature
title_full_unstemmed Leiomyosarcoma of the small bowel: Report of a case and review of the literature
title_short Leiomyosarcoma of the small bowel: Report of a case and review of the literature
title_sort leiomyosarcoma of the small bowel: report of a case and review of the literature
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4334955/
https://www.ncbi.nlm.nih.gov/pubmed/25506852
http://dx.doi.org/10.1016/j.ijscr.2014.11.009
work_keys_str_mv AT luisjoshua leiomyosarcomaofthesmallbowelreportofacaseandreviewoftheliterature
AT ejtehadifarshid leiomyosarcomaofthesmallbowelreportofacaseandreviewoftheliterature
AT howlettdavidc leiomyosarcomaofthesmallbowelreportofacaseandreviewoftheliterature
AT donnellanimeldam leiomyosarcomaofthesmallbowelreportofacaseandreviewoftheliterature