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Analysis of significantly mutated genes as a clinical tool for the diagnosis in a case of lung cancer
Bronchoendoscopic examination is not necessarily comfortable procedure and limited by its sensitivity, depending on the location and size of the tumor lesion. Patients with a non-diagnostic bronchoendoscopic examination often undergo further invasive examinations. Non-invasive diagnostic tool of lun...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5328745/ https://www.ncbi.nlm.nih.gov/pubmed/28275538 http://dx.doi.org/10.1016/j.rmcr.2017.02.008 |
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author | Miyashita, Yoshihiro Hirotsu, Yosuke Tsutsui, Toshiharu Higashi, Seishi Sogami, Yusuke Kakizaki, Yumiko Goto, Taichiro Amemiya, Kenji Oyama, Toshio Omata, Masao |
author_facet | Miyashita, Yoshihiro Hirotsu, Yosuke Tsutsui, Toshiharu Higashi, Seishi Sogami, Yusuke Kakizaki, Yumiko Goto, Taichiro Amemiya, Kenji Oyama, Toshio Omata, Masao |
author_sort | Miyashita, Yoshihiro |
collection | PubMed |
description | Bronchoendoscopic examination is not necessarily comfortable procedure and limited by its sensitivity, depending on the location and size of the tumor lesion. Patients with a non-diagnostic bronchoendoscopic examination often undergo further invasive examinations. Non-invasive diagnostic tool of lung cancer is desired. A 72-year-old man had a 3.0 cm × 2.5 cm mass lesion in the segment B1 of right lung. Cytological examination of sputum, bronchial washing and curetted samples were all “negative”. We could confirm a diagnosis of lung cancer after right upper lung lobe resection pathologically, and also obtained concordant results by genomic analysis using cytological negative samples from airways collected before operation. Genetic analysis showed mutational profiles of both resected specimens and samples from airways were identical. These data clearly indicated the next generation sequencing (NGS) may yield a diagnostic tool to conduct “precision medicine”. |
format | Online Article Text |
id | pubmed-5328745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-53287452017-03-08 Analysis of significantly mutated genes as a clinical tool for the diagnosis in a case of lung cancer Miyashita, Yoshihiro Hirotsu, Yosuke Tsutsui, Toshiharu Higashi, Seishi Sogami, Yusuke Kakizaki, Yumiko Goto, Taichiro Amemiya, Kenji Oyama, Toshio Omata, Masao Respir Med Case Rep Case Report Bronchoendoscopic examination is not necessarily comfortable procedure and limited by its sensitivity, depending on the location and size of the tumor lesion. Patients with a non-diagnostic bronchoendoscopic examination often undergo further invasive examinations. Non-invasive diagnostic tool of lung cancer is desired. A 72-year-old man had a 3.0 cm × 2.5 cm mass lesion in the segment B1 of right lung. Cytological examination of sputum, bronchial washing and curetted samples were all “negative”. We could confirm a diagnosis of lung cancer after right upper lung lobe resection pathologically, and also obtained concordant results by genomic analysis using cytological negative samples from airways collected before operation. Genetic analysis showed mutational profiles of both resected specimens and samples from airways were identical. These data clearly indicated the next generation sequencing (NGS) may yield a diagnostic tool to conduct “precision medicine”. Elsevier 2017-02-17 /pmc/articles/PMC5328745/ /pubmed/28275538 http://dx.doi.org/10.1016/j.rmcr.2017.02.008 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Miyashita, Yoshihiro Hirotsu, Yosuke Tsutsui, Toshiharu Higashi, Seishi Sogami, Yusuke Kakizaki, Yumiko Goto, Taichiro Amemiya, Kenji Oyama, Toshio Omata, Masao Analysis of significantly mutated genes as a clinical tool for the diagnosis in a case of lung cancer |
title | Analysis of significantly mutated genes as a clinical tool for the diagnosis in a case of lung cancer |
title_full | Analysis of significantly mutated genes as a clinical tool for the diagnosis in a case of lung cancer |
title_fullStr | Analysis of significantly mutated genes as a clinical tool for the diagnosis in a case of lung cancer |
title_full_unstemmed | Analysis of significantly mutated genes as a clinical tool for the diagnosis in a case of lung cancer |
title_short | Analysis of significantly mutated genes as a clinical tool for the diagnosis in a case of lung cancer |
title_sort | analysis of significantly mutated genes as a clinical tool for the diagnosis in a case of lung cancer |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5328745/ https://www.ncbi.nlm.nih.gov/pubmed/28275538 http://dx.doi.org/10.1016/j.rmcr.2017.02.008 |
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