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Пульмонология

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Описание случая семейного идиопатического легочного фиброза

https://doi.org/10.18093/0869-0189-2009-6-112-117

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Об авторах

О. А. Цветкова
ГОУ ВПО "Московская медицинская академия им. И.М.Сеченова Росздрава"
Россия


Е. Ф. Рогова
ГОУ ВПО "Московская медицинская академия им. И.М.Сеченова Росздрава"
Россия


О. О. Воронкова
ГОУ ВПО "Московская медицинская академия им. И.М.Сеченова Росздрава"
Россия


О. Ю. Агапова
ГОУ ВПО "Московская медицинская академия им. И.М.Сеченова Росздрава"
Россия


Э. В. Генерозов
ФГУ НИИ физико-химической медицины Росздрава
Россия


Список литературы

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.


Для цитирования:


Цветкова О.А., Рогова Е.Ф., Воронкова О.О., Агапова О.Ю., Генерозов Э.В. Описание случая семейного идиопатического легочного фиброза. Пульмонология. 2009;(6):112-117. https://doi.org/10.18093/0869-0189-2009-6-112-117

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ISSN 0869-0189 (Print)
ISSN 2541-9617 (Online)