Bouros Demosthenes, Hatzakis Kostas, Labrakis Haris, Zeibecoglou Kyriaki
Department of Pneumonology, Medical School University of Crete, Crete, Greece.
Chest. 2002 Apr;121(4):1278-89. doi: 10.1378/chest.121.4.1278.
A number of studies have shown a high incidence of lung cancer in patients with idiopathic pulmonary fibrosis (9.8 to 38%) compared to control subjects (2 to 6.4%). A similar trend occurs in other entities that affect the interstitial lung compartment, such as systemic sclerosis and sarcoidosis, as well as occupational diseases. The pathogenesis of lung cancer in patients with diffuse pulmonary fibrosis is still unclear. Recent progress in molecular and cellular biology has shed some light on the possible interactions of several types of inflammatory cells, following the deleterious effects of toxic factors leading to alveolitis, and destruction and disorganization of lung parenchyma, which results in fibrosis. Further research in the field would enhance our understanding of the pathogenic mechanisms of cancer development in these patients, and to explain the reason for the different incidence of lung cancer in patients with various interstitial lung diseases.
多项研究表明,与对照人群(2%至6.4%)相比,特发性肺纤维化患者的肺癌发病率较高(9.8%至38%)。在其他影响肺间质的疾病中,如系统性硬化症和结节病以及职业病,也出现了类似的趋势。弥漫性肺纤维化患者肺癌的发病机制仍不清楚。分子和细胞生物学的最新进展对几种炎症细胞的可能相互作用有所揭示,这些炎症细胞是在导致肺泡炎的毒性因子产生有害作用以及肺实质破坏和结构紊乱(从而导致纤维化)之后出现的。该领域的进一步研究将增进我们对这些患者癌症发生致病机制的理解,并解释不同间质性肺疾病患者肺癌发病率不同的原因。