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Gastrointestinal stromal tumor
BACKGROUND: GISTs are a subset of mesenchymal tumors and represent the most common mesenchymal neoplasms of GI tract. However, GIST is a recently recognized tumor entity and the literature on these stromal tumors has rapidly expanded. METHODS: An extensive review of the literature was carried out in...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2749031/ https://www.ncbi.nlm.nih.gov/pubmed/19646278 http://dx.doi.org/10.1186/1477-7819-7-61 |
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author | Stamatakos, Michael Douzinas, Emmanouel Stefanaki, Charikleia Safioleas, Panagiotis Polyzou, Electra Levidou, Georgia Safioleas, Michael |
author_facet | Stamatakos, Michael Douzinas, Emmanouel Stefanaki, Charikleia Safioleas, Panagiotis Polyzou, Electra Levidou, Georgia Safioleas, Michael |
author_sort | Stamatakos, Michael |
collection | PubMed |
description | BACKGROUND: GISTs are a subset of mesenchymal tumors and represent the most common mesenchymal neoplasms of GI tract. However, GIST is a recently recognized tumor entity and the literature on these stromal tumors has rapidly expanded. METHODS: An extensive review of the literature was carried out in both online medical journals and through Athens University Medical library. An extensive literature search for papers published up to 2009 was performed, using as key words, GIST, Cajal's cells, treatment, Imatinib, KIT, review of each study were conducted, and data were abstracted. RESULTS: GIST has recently been suggested that is originated from the multipotential mesenchymal stem cells. It is estimated that the incidence of GIST is approximately 10-20 per million people, per year. CONCLUSION: The clinical presentation of GIST is variable but the most usual symptoms include the presence of a mass or bleeding. Surgical resection of the local disease is the mainstay therapy. However, therapeutic agents, such as Imatinib have now been approved for the treatment of advanced GISTs and others, such as everolimus, rapamycin, heat shock protein 90 and IGF are in trial stage demonstrate promising results for the management of GISTs. |
format | Text |
id | pubmed-2749031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27490312009-09-23 Gastrointestinal stromal tumor Stamatakos, Michael Douzinas, Emmanouel Stefanaki, Charikleia Safioleas, Panagiotis Polyzou, Electra Levidou, Georgia Safioleas, Michael World J Surg Oncol Review BACKGROUND: GISTs are a subset of mesenchymal tumors and represent the most common mesenchymal neoplasms of GI tract. However, GIST is a recently recognized tumor entity and the literature on these stromal tumors has rapidly expanded. METHODS: An extensive review of the literature was carried out in both online medical journals and through Athens University Medical library. An extensive literature search for papers published up to 2009 was performed, using as key words, GIST, Cajal's cells, treatment, Imatinib, KIT, review of each study were conducted, and data were abstracted. RESULTS: GIST has recently been suggested that is originated from the multipotential mesenchymal stem cells. It is estimated that the incidence of GIST is approximately 10-20 per million people, per year. CONCLUSION: The clinical presentation of GIST is variable but the most usual symptoms include the presence of a mass or bleeding. Surgical resection of the local disease is the mainstay therapy. However, therapeutic agents, such as Imatinib have now been approved for the treatment of advanced GISTs and others, such as everolimus, rapamycin, heat shock protein 90 and IGF are in trial stage demonstrate promising results for the management of GISTs. BioMed Central 2009-08-01 /pmc/articles/PMC2749031/ /pubmed/19646278 http://dx.doi.org/10.1186/1477-7819-7-61 Text en Copyright © 2009 Stamatakos 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 cited. |
spellingShingle | Review Stamatakos, Michael Douzinas, Emmanouel Stefanaki, Charikleia Safioleas, Panagiotis Polyzou, Electra Levidou, Georgia Safioleas, Michael Gastrointestinal stromal tumor |
title | Gastrointestinal stromal tumor |
title_full | Gastrointestinal stromal tumor |
title_fullStr | Gastrointestinal stromal tumor |
title_full_unstemmed | Gastrointestinal stromal tumor |
title_short | Gastrointestinal stromal tumor |
title_sort | gastrointestinal stromal tumor |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2749031/ https://www.ncbi.nlm.nih.gov/pubmed/19646278 http://dx.doi.org/10.1186/1477-7819-7-61 |
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