Combined Pulmonary Fibrosis and Emphysema: Comparative Evidence on a Complex Condition

被引:11
作者
Calaras, Diana [1 ]
Mathioudakis, Alexander G. [2 ]
Lazar, Zsofia [3 ]
Corlateanu, Alexandru [1 ]
机构
[1] State Univ Med & Pharm Nicolae Testemitanu, Dept Pulmonol & Allergol, MD-2004 Kishinev, Moldova
[2] Univ Manchester, Sch Biol Sci, Div Immunol Immun Infect & Resp Med, Manchester M13 9PL, England
[3] Semmelweis Univ, Dept Pulmonol, H-1083 Budapest, Hungary
关键词
emphysema; lung fibrosis; interstitial lung disease; lung function; pulmonary hypertension; LUNG-CANCER; CLINICAL CHARACTERISTICS; CIGARETTE-SMOKING; HYPERTENSION; DISEASE; COPD; ASSOCIATION; MECHANISMS; SUSCEPTIBILITY; EFFICACY;
D O I
10.3390/biomedicines11061636
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Combined pulmonary fibrosis and emphysema (CPFE) is a clinical syndrome characterized by upper lobe emphysema and lower lobe fibrosis manifested by exercise hypoxemia, normal lung volumes, and severe reduction of diffusion capacity of carbon monoxide. It has varying prevalence worldwide with a male predominance, and with smoking history of more than 40 pack-years being a common risk factor. The unique imaging features of CPFE emphasize its distinct entity, aiding in the timely detection of pulmonary hypertension and lung cancer, both of which are common complications. High-resolution computed tomography (HRCT) is an important diagnostic and prognostic tool, while lung cancer is an independent factor that alters the prognosis in CPFE patients. Treatment options for CPFE are limited, but smoking cessation, usual treatments of pulmonary fibrosis and emphysema, and avoidance of environmental exposures are encouraged.
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页数:14
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