Описание случая семейного идиопатического легочного фиброза
https://doi.org/10.18093/0869-0189-2009-6-112-117
Keywords
УДК 616.24-004-07
About the Authors
О. ЦветковаRussian Federation
Е. Рогова
Russian Federation
О. Воронкова
Russian Federation
О. Агапова
Russian Federation
Э. Генерозов
Russian Federation
References
1. Grutters J.C., Bois R.M. Genetics of fibrosing lung diseases. Eur. Respir. J. 2005; 25: 915-927.
2. Steel M.P., Speer M.C., Loyd J.E. et al. Familian pulmonary fibrosis (FPF) in the United States: clinical characteristics and patterns of inheritance. Am. J. Respir. Crit. Care Med. 2004; 169: A550.
3. Thomas A.Q., Lane K., Phillips J. III et al. Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred. Am. J. Respir. Crit. Care Med. 2002; 165: 1322-1328.
4. Armanios M.Y., Chen J.J., Cogan J.D. et al. Telomerase mutations in families with idiopathic pulmonary fibrosis. N. Engl. J. Med. 2007; 356 (13): 1317-1326.
5. Coultas D.B., Zumwalt R.E., Black W.C., Sobonya R.E. The epidemiology of interstitial lung diseases. Am. J. Respir. Crit. Care Med. 1994; 150 (4): 967-972.
6. Dishop M.K., Langston C. Pathology of diffuse lung disease in infancy. In: Patology of the lung. Edited by W.Timens and H.H.Popper. ERS. Volume 12. Monograph 39, March 2007.
7. Meltzer E.B., Noble P.W. Idiopathic pulmonary fibrosis. Orphanet J. Rare Dis. 2008; 3: 8.
8. Chibbar R., Shih F., Baga M. et al. Nonspecific interstitial pneumonia and usual interstitial pneumonia with mutation in surfactant protein C in familial pulmonary fibrosis. Mod. Patthol. 2004; 17: 973-980.
9. Lawson W.E., Grant S.W., Ambrosini V. et al. Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF. Thorax 2004; 59: 977-980.
10. Loyd J.E. Pulmonary fibrosis in families. Am. J. Respir. Cell Mol. Biol. 2003; 29 (suppl. 3): S47-S50.
11. Musk A.W., Zilko P.J., Manners P. et al. Genetic studies in familial fibrosing alveolitis. Possible linkage with immunoglobulin allotypes (Gm). Chest 1986; 89: 206-210.
12. Coultas D.B., Zumwalt R.E., Black W.C., Sobonya RE. The epidemiology of interstitial lung diseases. Am. J. Respir. Crit. Care Med. 1994; 150: 967-972.
13. Marshall R.P., Puddicombe A., Cookson W.O., Laurent G.J. Adult familial cryptogenic fibrosing alveolitis in the United Kingdom. Thorax 2000; 55: 143-146.
14. Selman M., King T.E., Pardo A. Idiopathic pulmonary fibrosis: prevailing and evolving hypotheses about its pathogenesis and implications for therapy. Ann. Intern. Med. 2001; 134: 136-151.
15. Selman M., Pardo A. The epithelial / fibroblastic pathway in the pathogenesis of idiopathic pulmonary fibrosis. Am. J. Respir. Cell Mol. Biol. 2003; 29 (suppl. 3): S93-S97.
16. Lawson W.E., Grant S.W., Ambrosini V. et al. Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF. Thorax 2004; 59: 977-980.
17. Fridlender Z.G., Cohen P.Y., Golan O. et al. Telomerase activity in bleomycin-induced epithelial cell apoptosis and lung fibrosis. Eur. Respir. J. 2007; 30: 205-213.
18. Lee H.&L., Ryu J.H., Wittmer M.H. et al. Familial idiopathic pulmonary fibrosis. Clinical features and outcome. Chest 2005; 127 (6): 2034-2041.
Review
For citations:
, , , , . PULMONOLOGIYA. 2009;(6):112-117. (In Russ.) https://doi.org/10.18093/0869-0189-2009-6-112-117