Cancers pulmonaires associés à une pathologie interstitielle pulmonaire fibrosante

Q4 Medicine
B. Duchemann , J. Cadranel , A. Paix , L. Matton , M. Didier , D. Radu , M. Kambouchner , K. Chouahnia , J. Behr , P.-Y. Brillet , H. Nunes
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引用次数: 0

Abstract

The occurrence of lung cancer in patients with diffuse fibrosing pneumonitis is neither fortuitous nor rare. Diagnosis strategy and therapeutics are currently poorly standardized, and there is no expert consensus available in Europe. Therapeutic strategy is limited by the poor underlying respiratory function, the risk of respiratory exacerbation favored by some treatments, age and comorbidities, and more generally by the underlying frailty of patients with lung fibrosis. In the current article we will review the epidemiology, the diagnosis management, and the necessary data for discussing local or systemic therapeutics.
与纤维性肺间质病变相关的肺癌
弥漫性纤维化肺炎患者发生肺癌既不是偶然的,也不是罕见的。诊断策略和治疗方法目前标准化程度很低,在欧洲没有专家共识。治疗策略受到以下因素的限制:潜在的呼吸功能差、某些治疗方法所青睐的呼吸恶化风险、年龄和合并症,以及更普遍的肺纤维化患者的潜在虚弱。在当前的文章中,我们将回顾流行病学,诊断管理,以及讨论局部或全身治疗的必要数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Revue des Maladies Respiratoires Actualites
Revue des Maladies Respiratoires Actualites Medicine-Pulmonary and Respiratory Medicine
CiteScore
0.10
自引率
0.00%
发文量
671
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