Morphological diagnosis of idiopathic pulmonary fibrosis
- Authors: Chernyaev A.L1, Samsonova M.V1
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Affiliations:
- Research Institute of Pulmonology of FMBA of Russia
- Issue: Vol 19, No 3 (2017)
- Pages: 14-16
- Section: Articles
- URL: https://ogarev-online.ru/2075-1753/article/view/94756
- ID: 94756
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Abstract
Modern views on the diagnosis of idiopathic interstitial pneumonia (IIP) are based on multidisciplinary approach. The paper considers main types of IIP, as well as the principles of their differential diagnosis. Idiopathic pulmonary fibrosis histologically referred to as usual interstitial pneumonia, in which diffuse fibrosis causes a restructuring of the parenchyma of the lungs.
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##article.viewOnOriginalSite##About the authors
A. L Chernyaev
Research Institute of Pulmonology of FMBA of Russia
Email: cheral12@gmail.com
д-р мед. наук, проф., зав. отд. патологии ФГБУ «НИИ пульмонологии» 105077, Russian Federation, Moscow, ul. 11-ia Parkovaia, d. 32, korp. 4
M. V Samsonova
Research Institute of Pulmonology of FMBA of Russia
Email: samary@mail.ru
д-р мед. наук, проф., зав. лаб. патологической анатомии и иммунологии ФБГУ «НИИ пульмонологии» 105077, Russian Federation, Moscow, ul. 11-ia Parkovaia, d. 32, korp. 4
References
- An Official American Thoracic Society/European Respiratory Society Statement: Update of the International Multidisciplinary Classification of the Idiopathic Interstitial Pneumonias Am J Respir Crit Care Med 2013; 188 (Iss. 6): 733-48.
- Nicholson A.G, Cagle P.T, Fraire A.E et al. Interstitial pneumonias. In: Dail and Hammar's Pulmonary Pathology. Springer Science + Business Media, LLC, 2008; p. 695-721.
- Agarwal R, Jindal S.K. Acute exacerbation of idiopathic pulmonary fibrosis: a systematic review. Eur J Intern Med 2008; 19: 227-35.
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