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Prevalence, risk factors and survival of lung cancer in the idiopathic pulmonary fibrosis

机译:特发性肺纤维化的肺癌患病率,危险因素和生存率

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摘要

AbstractBackground:  The aim of this study was to evaluate the prevalence, risk factors, and survival of lung cancer in patients with idiopathic pulmonary fibrosis (IPF).Methods:  IPF with lung cancer from tertiary hospitals consisted of 1685 patients who had been diagnosed between 2003 and 2007. We reviewed their medical records retrospectively to evaluate the prevalence, risk factors and prognosis of lung cancer in IPF patients.Results:  Among all patients with IPF, 114 cases (6.8%) had lung cancer with IPF. The incidence of lung cancer in patients with IPF was 1.03 persons per 100 person-year (25 patients/2408 years). Most cases of lung cancer (73/114, 68.9%) were located in IPF-associated areas; the lung cancer typically developed in peripheral and lower lobe areas. The study revealed that forced vital capacity (% predicted) at the initial diagnosis and development of lung cancer were independent prognostic factors in patients with IPF.Conclusions:  Lung cancer in patients with IPF was significantly related with the IPF prognosis. An active evaluation should be performed in patients with IPF to detect lung cancer early.
机译:摘要背景:本研究旨在评估特发性肺纤维化(IPF)患者的肺癌患病率,危险因素和生存率。和2007年。我们回顾性地回顾了他们的病历,以评估IPF患者的肺癌患病率,危险因素和预后。结果:在所有IPF患者中,有114例(6.8%)患有IPF肺癌。 IPF患者的肺癌发生率为每100人年1.03人(25位患者/ 2408年)。多数肺癌病例(73 / 114,68.9%)位于与IPF相关的地区。肺癌通常发生在周围和下叶区域。该研究表明,在肺癌的初始诊断和发展过程中,强迫肺活量(预测值的百分比)是IPF患者的独立预后因素。结论:IPF患者的肺癌与IPF预后密切相关。对IPF患者应进行积极评估,以及早发现肺癌。

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