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Combined pulmonary fibrosis and emphysema (CPFE): an entity different from emphysema or pulmonary fibrosis alone

机译:合并肺纤维化和肺气肿(CPFE):与单独的肺气肿或肺纤维化不同的实体

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摘要

Chronic obstructive pulmonary disease (COPD) and idiopathic interstitial pneumonias (IIP), with different radiological, pathological, functional and prognostic characteristics, have been regarded as separate entities for a long time. However, there is an increasing recognition of the coexistence of emphysema and pulmonary fibrosis in individuals. The association was first described as a syndrome by Cottin in 2005, named “combined pulmonary fibrosis and emphysema (CPFE)”, which is characterized by exertional dyspnea, upper-lobe emphysema and lower-lobe fibrosis, preserved lung volume and severely diminished capacity of gas exchange. CPFE is frequently complicated by pulmonary hypertension, acute lung injury and lung cancer and prognosis of it is poor. Treatments for CPFE patients with severe pulmonary hypertension are less effective other than lung transplantation. However, CPFE has not yet attracted wide attention of clinicians and there is no research systematically contrasting the differences among CPFE, emphysema/COPD and IIP at the same time. The authors will review the existing knowledge of CPFE and compare them to either entity alone for the first time, with the purpose of improving the awareness of this syndrome and exploring novel effective therapeutic strategies in clinical practice.
机译:慢性阻塞性肺疾病(COPD)和特发性间质性肺炎(IIP)具有不同的放射学,病理学,功能和预后特征,长期以来一直被视为独立的个体。然而,人们越来越认识到肺气肿和肺纤维化并存。该协会在2005年被Cottin首次描述为一种综合征,称为“肺纤维化和肺气肿合并症(CPFE)”,其特征是劳累性呼吸困难,上叶肺气肿和下叶纤维化,肺体积得以保留,且肺活量严重降低。气体交换。 CPFE通常并发肺动脉高压,急性肺损伤和肺癌,预后差。 CPFE重度肺动脉高压患者的治疗效果比肺移植效果差。然而,CPFE尚未引起临床医生的广泛关注,也没有系统地同时对比CPFE,肺气肿/ COPD和IIP之间差异的研究。作者将回顾CPFE的现有知识,并首次将它们与任何一个实体进行比较,以提高对该综合征的认识并探索临床实践中新颖的有效治疗策略。

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