摘要: The development of pulmonary fibrosis is the end point a wide range respiratory diseases including organic and inorganic dust exposure, infection, acute lung injury, radiation, idiopathic interstitial pneumonias (IIP), connective tissue diseases. most common fibrotic disorder (IPF), an IIP with histological appearance usual pneumonia (UIP). Formerly also known as cryptogenic fibrosing alveolitis (CFA), definition this disease has evolved in recent years to exclude non-specific (NSIP), sub-type more diffuse fibrosis, different clinical course better prognosis than IPF. This change must be considered when looking at historical studies that grouped UIP NSIP under same umbrella term.
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Ludwicka A, Trojanowska M, Strange C, Smith Ea, Leroy Ec, Korn Jh, Silver Rm, Smith T, Baumann M, Growth and characterization of fibroblasts obtained from bronchoalveolar lavage of patients with scleroderma. The Journal of Rheumatology. ,vol. 19, pp. 1716- 1723 ,(1992)
Constance Barazzone-Argiroffo, Patrick Muzzin, Yves R. Donati, Chen-Da Kan, Michel L. Aubert, Pierre-François Piguet, Hyperoxia increases leptin production: a mechanism mediated through endogenous elevation of corticosterone American Journal of Physiology-lung Cellular and Molecular Physiology. ,vol. 281, ,(2001) , 10.1152/AJPLUNG.2001.281.5.L1150
J. E. Weiland, J. G. Garcia, W. B. Davis, J. E. Gadek, Neutrophil collagenase in rheumatoid interstitial lung disease. Journal of Applied Physiology. ,vol. 62, pp. 628- 633 ,(1987) , 10.1152/JAPPL.1987.62.2.628
Lucey Ec, Celli Br, Goldstein Rh, Snider Gl, O'Brien Jj, Chronic interstitial pulmonary fibrosis produced in hamsters by endotracheal bleomycin. Lung volumes, volume-pressure relations, carbon monoxide uptake, and arterial blood gas studied. The American review of respiratory disease. ,vol. 117, pp. 289- ,(1978) , 10.1164/ARRD.1978.117.2.289
Anthony S. Fauci, Gary W. Hunninghake, Pulmonary Involvement in the Collagen Vascular Diseases1,2 The American review of respiratory disease. ,vol. 119, pp. 471- 503 ,(2015) , 10.1164/ARRD.1979.119.3.471
P J Townsend, B Thompson, E J Holborow, I Mohammed, P L Haslam, M Turner-Warwick, M E Hodson, Circulating immune complexes in patients with cryptogenic fibrosing alveolitis. Clinical and Experimental Immunology. ,vol. 37, pp. 381- 390 ,(1979)
Winzler C, Ricciardi-Castagnoli P, Girolomoni G, Riva S, Nolli Ml, Lutz Mb, Citterio S, Bacteria and bacterial cell wall constituents induce the production of regulatory cytokines in dendritic cell clones. Journal of Inflammation. ,vol. 46, pp. 98- 105 ,(1996)
Does idiopathic pulmonary fibrosis increase lung cancer risk American Journal of Respiratory and Critical Care Medicine. ,vol. 161, pp. 1- 2 ,(2000) , 10.1164/AJRCCM.161.1.ED14-99
R S Thrall, R M Jack, J R McCormick, R A McReynolds, P A Ward, Bleomycin-induced pulmonary fibrosis in the rat: inhibition by indomethacin. American Journal of Pathology. ,vol. 95, pp. 117- 130 ,(1979)
Richard Bucala, Lori A. Spiegel, Jason Chesney, Margaret Hogan, Anthony Cerami, Circulating fibrocytes define a new leukocyte subpopulation that mediates tissue repair. Molecular Medicine. ,vol. 1, pp. 71- 81 ,(1994) , 10.1007/BF03403533