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肺肉瘤样癌的诊治现状

Pulmonary sarcomatoid carcinoma (PSC) is a rare, poorly differentiated, subtype of non-small cell lung carcinoma (NSCLC) and constitutes approximately 0.1% to 0.5% of all lung malignancies. PSC can be divided into five subtypes based on the 2015 World Health Organization (WHO) classification of lung...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318565/
https://www.ncbi.nlm.nih.gov/pubmed/30591097
http://dx.doi.org/10.3779/j.issn.1009-3419.2018.12.07
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description Pulmonary sarcomatoid carcinoma (PSC) is a rare, poorly differentiated, subtype of non-small cell lung carcinoma (NSCLC) and constitutes approximately 0.1% to 0.5% of all lung malignancies. PSC can be divided into five subtypes based on the 2015 World Health Organization (WHO) classification of lung tumors: pleomorphic carcinoma, spindle cell carcinoma, giant cell carcinoma, carcinosarcoma, and pulmonary blastoma. Some imaging characteristics can be found for PSC although no special symptoms. The accurate pathological diagnosis of PSC can be a significant challenge, which depends on pathology and immunohistochemistry. PSC should be managed similar to other NSCLC, surgical resection is the standard management for early stage cases, moreover, multimodal treatment should be considered. However, PSC is insensitive to radiotherapy and chemotherapy, and has high rate of local and metastatic recurrence and poor prognosis. With the development of molecular pathology, targeted therapy and immunotherapy may have broad prospects.
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spelling pubmed-63185652019-01-14 肺肉瘤样癌的诊治现状 Zhongguo Fei Ai Za Zhi 综述 Pulmonary sarcomatoid carcinoma (PSC) is a rare, poorly differentiated, subtype of non-small cell lung carcinoma (NSCLC) and constitutes approximately 0.1% to 0.5% of all lung malignancies. PSC can be divided into five subtypes based on the 2015 World Health Organization (WHO) classification of lung tumors: pleomorphic carcinoma, spindle cell carcinoma, giant cell carcinoma, carcinosarcoma, and pulmonary blastoma. Some imaging characteristics can be found for PSC although no special symptoms. The accurate pathological diagnosis of PSC can be a significant challenge, which depends on pathology and immunohistochemistry. PSC should be managed similar to other NSCLC, surgical resection is the standard management for early stage cases, moreover, multimodal treatment should be considered. However, PSC is insensitive to radiotherapy and chemotherapy, and has high rate of local and metastatic recurrence and poor prognosis. With the development of molecular pathology, targeted therapy and immunotherapy may have broad prospects. 中国肺癌杂志编辑部 2018-12-20 /pmc/articles/PMC6318565/ /pubmed/30591097 http://dx.doi.org/10.3779/j.issn.1009-3419.2018.12.07 Text en 版权所有©《中国肺癌杂志》编辑部2018 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/
spellingShingle 综述
肺肉瘤样癌的诊治现状
title 肺肉瘤样癌的诊治现状
title_full 肺肉瘤样癌的诊治现状
title_fullStr 肺肉瘤样癌的诊治现状
title_full_unstemmed 肺肉瘤样癌的诊治现状
title_short 肺肉瘤样癌的诊治现状
title_sort 肺肉瘤样癌的诊治现状
topic 综述
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318565/
https://www.ncbi.nlm.nih.gov/pubmed/30591097
http://dx.doi.org/10.3779/j.issn.1009-3419.2018.12.07
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