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Combined Pulmonary Fibrosis and Emphysema Syndrome: A New Phenotype within the Spectrum of Smoking-Related Interstitial Lung Disease

机译:合并肺纤维化和肺气肿综合征:吸烟相关间质性肺疾病谱内的新表型

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Combined pulmonary fibrosis and emphysema (CPFE) is a recently defined syndrome, in which centrilobular and/or paraseptal emphysemas in upper lung zones coexist with pulmonary fibrosis in lower lobes in individuals. These patients have a characteristic lung function profile, with unexpected subnormal dynamic and static lung volumes, contrasting with a significant reduction of carbon monoxide transfer (DLco) and exercise hypoxemia. Pulmonary hypertension is highly prevalent in CPFE and is the leading determinant of death. Tobacco smoking has been proposed as the main factor in its etiology, though the pathophysiology and its natural history remain to be determined. High-resolution computed axial tomography is the mandatory tool to confirm the diagnosis. Currently, there is no consensus about its treatment since those published to date on this issue are limited to well-characterised series of cases; hence, a better understanding of this entity may help in the development of future therapeutic approaches.
机译:合并肺纤维化和肺气肿(CPFE)是一种最近定义的综合征,其中上肺区的小叶和/或隔隔肺气肿与个体下叶的肺纤维化并存。这些患者具有特征性的肺功能特征,具有出乎意料的动态和静态肺活量,与之相比,一氧化碳转移(DLco)和运动性低氧血症显着减少。肺动脉高压在CPFE中非常普遍,是死亡的主要决定因素。吸烟已被认为是其病因的主要因素,尽管其病理生理及其自然史尚待确定。高分辨率计算机轴向断层扫描是确认诊断的必不可少的工具。目前,关于其治疗方法尚无共识,因为迄今为止在该问题上发表的文献仅限于特征明确的一系列病例;因此,对该实体的更好理解可能有助于未来治疗方法的发展。

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