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The clinicopathological study of lung cancer concealed in end-stage of interstitial lung disease
BACKGROUND: Most of the patients with interstitial lung disease (ILD) complicated with lung cancer (ILD-LC) showed non-specific clinical manifestations. This study is to explore the incidence of lung cancer concealed in the end-stage of interstitial lung disease (LC-CES-ILD). METHODS: A total of 154...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798808/ https://www.ncbi.nlm.nih.gov/pubmed/35117398 http://dx.doi.org/10.21037/tcr.2019.11.36 |
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author | Wang, Bei Zhang, Xiaoyan Chen, Huang Yang, Lei Li, Jie Xiao, Fei Liang, Chaoyang Zhong, Dingrong |
author_facet | Wang, Bei Zhang, Xiaoyan Chen, Huang Yang, Lei Li, Jie Xiao, Fei Liang, Chaoyang Zhong, Dingrong |
author_sort | Wang, Bei |
collection | PubMed |
description | BACKGROUND: Most of the patients with interstitial lung disease (ILD) complicated with lung cancer (ILD-LC) showed non-specific clinical manifestations. This study is to explore the incidence of lung cancer concealed in the end-stage of interstitial lung disease (LC-CES-ILD). METHODS: A total of 154 cases of lung transplantation from March 2017 to December 2018 were studied retrospectively, of which 7 cases were found to be LC-CES-ILD. Serum tumor biomarkers were examined. HE and immunohistochemical staining were performed for the tumor tissue after the operation. Lung cancer (LC) drive gene was detected by quantitative real-time polymerase chain reaction (qRT-PCR). RESULTS: The percentage of male patients with idiopathic pulmonary fibrosis (IPF) was 44.81%. The expression of all tumor biomarkers was significantly increased in 6 patients with LC-CES-ILD. After operation, apparent destruction of lung tissue structure was observed in 7 patients, and honeycomb appearance could be seen in some areas. After HE staining, 4 cases of acinar type and 2 cases of mucinous adenocarcinoma were found. The results of molecular pathology showed that only one case of mucinous adenocarcinoma had KRAS mutation, and no mutation of LC co-driving gene was found in the rest of the cases. CONCLUSIONS: It is necessary to detect the lung tissue of patients with end-stage ILD, which were probably correlated with the occurrence of LC concealed, before lung transplantation. |
format | Online Article Text |
id | pubmed-8798808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87988082022-02-02 The clinicopathological study of lung cancer concealed in end-stage of interstitial lung disease Wang, Bei Zhang, Xiaoyan Chen, Huang Yang, Lei Li, Jie Xiao, Fei Liang, Chaoyang Zhong, Dingrong Transl Cancer Res Original Article BACKGROUND: Most of the patients with interstitial lung disease (ILD) complicated with lung cancer (ILD-LC) showed non-specific clinical manifestations. This study is to explore the incidence of lung cancer concealed in the end-stage of interstitial lung disease (LC-CES-ILD). METHODS: A total of 154 cases of lung transplantation from March 2017 to December 2018 were studied retrospectively, of which 7 cases were found to be LC-CES-ILD. Serum tumor biomarkers were examined. HE and immunohistochemical staining were performed for the tumor tissue after the operation. Lung cancer (LC) drive gene was detected by quantitative real-time polymerase chain reaction (qRT-PCR). RESULTS: The percentage of male patients with idiopathic pulmonary fibrosis (IPF) was 44.81%. The expression of all tumor biomarkers was significantly increased in 6 patients with LC-CES-ILD. After operation, apparent destruction of lung tissue structure was observed in 7 patients, and honeycomb appearance could be seen in some areas. After HE staining, 4 cases of acinar type and 2 cases of mucinous adenocarcinoma were found. The results of molecular pathology showed that only one case of mucinous adenocarcinoma had KRAS mutation, and no mutation of LC co-driving gene was found in the rest of the cases. CONCLUSIONS: It is necessary to detect the lung tissue of patients with end-stage ILD, which were probably correlated with the occurrence of LC concealed, before lung transplantation. AME Publishing Company 2020-02 /pmc/articles/PMC8798808/ /pubmed/35117398 http://dx.doi.org/10.21037/tcr.2019.11.36 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Original Article Wang, Bei Zhang, Xiaoyan Chen, Huang Yang, Lei Li, Jie Xiao, Fei Liang, Chaoyang Zhong, Dingrong The clinicopathological study of lung cancer concealed in end-stage of interstitial lung disease |
title | The clinicopathological study of lung cancer concealed in end-stage of interstitial lung disease |
title_full | The clinicopathological study of lung cancer concealed in end-stage of interstitial lung disease |
title_fullStr | The clinicopathological study of lung cancer concealed in end-stage of interstitial lung disease |
title_full_unstemmed | The clinicopathological study of lung cancer concealed in end-stage of interstitial lung disease |
title_short | The clinicopathological study of lung cancer concealed in end-stage of interstitial lung disease |
title_sort | clinicopathological study of lung cancer concealed in end-stage of interstitial lung disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798808/ https://www.ncbi.nlm.nih.gov/pubmed/35117398 http://dx.doi.org/10.21037/tcr.2019.11.36 |
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