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原发性肺肉瘤19例临床分析
BACKGROUND AND OBJECTIVE: Primary pulmonary sarcoma (PPS) is a rare malignant tumor that originates from the mesenchymal tissue of the lungs. PPS is often easily misdiagnosed. This study aims to explore the clinical characteristics of PPS and provide a more comprehensive reference for the early diag...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
Publicado: |
中国肺癌杂志编辑部
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000307/ https://www.ncbi.nlm.nih.gov/pubmed/22681925 http://dx.doi.org/10.3779/j.issn.1009-3419.2012.06.09 |
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collection | PubMed |
description | BACKGROUND AND OBJECTIVE: Primary pulmonary sarcoma (PPS) is a rare malignant tumor that originates from the mesenchymal tissue of the lungs. PPS is often easily misdiagnosed. This study aims to explore the clinical characteristics of PPS and provide a more comprehensive reference for the early diagnosis and treatment of this disease. METHODS: The 1996 to 2011 clinical data of 19 cases with PPS in West China Hospital were presented, along with literature review. RESULTS: A total of 19 patients, which include 12 males, were presented in this study. Patients with age between 41 and 68 years accounted for 57.9% (the mean age was 41 years). The main clinical manifestations were cough, expectoration, and hemoptysis. Based on the imaging results, spiculation was found in eight cases and lobulation in five cases. The main pathologic types were synovial sarcoma, leiomyosarcoma, and malignant fibrous histiocytoma. Seventeen patients underwent surgery, whereas one patient underwent chemotherapy. All 17 cases with a median survival of 18 months were investigated after being discharged (follow-up rate: 89.5%). CONCLUSION: The clinical and imaging features of PPS are not characteristic. Thus, PPS is easily misdiagnosed and can cause high mortality among patients. |
format | Online Article Text |
id | pubmed-6000307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | 中国肺癌杂志编辑部 |
record_format | MEDLINE/PubMed |
spelling | pubmed-60003072018-07-06 原发性肺肉瘤19例临床分析 Zhongguo Fei Ai Za Zhi 临床经验 BACKGROUND AND OBJECTIVE: Primary pulmonary sarcoma (PPS) is a rare malignant tumor that originates from the mesenchymal tissue of the lungs. PPS is often easily misdiagnosed. This study aims to explore the clinical characteristics of PPS and provide a more comprehensive reference for the early diagnosis and treatment of this disease. METHODS: The 1996 to 2011 clinical data of 19 cases with PPS in West China Hospital were presented, along with literature review. RESULTS: A total of 19 patients, which include 12 males, were presented in this study. Patients with age between 41 and 68 years accounted for 57.9% (the mean age was 41 years). The main clinical manifestations were cough, expectoration, and hemoptysis. Based on the imaging results, spiculation was found in eight cases and lobulation in five cases. The main pathologic types were synovial sarcoma, leiomyosarcoma, and malignant fibrous histiocytoma. Seventeen patients underwent surgery, whereas one patient underwent chemotherapy. All 17 cases with a median survival of 18 months were investigated after being discharged (follow-up rate: 89.5%). CONCLUSION: The clinical and imaging features of PPS are not characteristic. Thus, PPS is easily misdiagnosed and can cause high mortality among patients. 中国肺癌杂志编辑部 2012-06-20 /pmc/articles/PMC6000307/ /pubmed/22681925 http://dx.doi.org/10.3779/j.issn.1009-3419.2012.06.09 Text en 版权所有©《中国肺癌杂志》编辑部2012 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 | 临床经验 原发性肺肉瘤19例临床分析 |
title | 原发性肺肉瘤19例临床分析 |
title_full | 原发性肺肉瘤19例临床分析 |
title_fullStr | 原发性肺肉瘤19例临床分析 |
title_full_unstemmed | 原发性肺肉瘤19例临床分析 |
title_short | 原发性肺肉瘤19例临床分析 |
title_sort | 原发性肺肉瘤19例临床分析 |
topic | 临床经验 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000307/ https://www.ncbi.nlm.nih.gov/pubmed/22681925 http://dx.doi.org/10.3779/j.issn.1009-3419.2012.06.09 |
work_keys_str_mv | AT yuánfāxìngfèiròuliú19lìlínchuángfēnxī AT yuánfāxìngfèiròuliú19lìlínchuángfēnxī |