Differential diagnosis of Interstitial Lung Diseases using Deep Learning networks

2020 ◽  
Vol 68 (3) ◽  
pp. 170-178
Author(s):  
V. N. Sukanya Doddavarapu ◽  
Giri Babu Kande ◽  
B. Prabhakara Rao
2020 ◽  
Vol 20 (2) ◽  
pp. 217-217 ◽  
Author(s):  
Miriana d’Alessandro ◽  
Alfonso Carleo ◽  
Paolo Cameli ◽  
Laura Bergantini ◽  
Anna Perrone ◽  
...  

2020 ◽  
Vol 92 (3) ◽  
pp. 102-108
Author(s):  
E. I. Shmelev ◽  
A. E. Ergeshov ◽  
V. Ya. Gergert

The review is devoted to the urgent problem of modern pulmonology: the differential diagnosis of idiopathic pulmonary fibrosis (ILF). ILF occupies a special place among many interstitial lung diseases for a number of reasons: 1) it is a deadly disease; 2) early diagnosis and adequate antifibrotic therapy significantly extend the life expectancy of patients; 3) anti-inflammatory drugs (corticosteroids) and cytostatics with ILF that are widely used in other forms of interstitial lung diseases are ineffective and accelerate the progression of the process; 4) the commonality of the main clinical signs (increasing respiratory failure) of various interstitial lung diseases. The list of respiratory diseases with which ILF should be differentiated is huge, and if with diffuse lung lesions of a known nature (disseminated pulmonary tuberculosis, pneumoconiosis, etc.) with a certain experience/qualification, the diagnosis is relatively simple, then the isolation of ILF from the group of idiopathic interstitial pneumonias always represents certain difficulties. The main methods used in the diagnosis of ILF are summarized taking into account current international and national recommendations.


2019 ◽  
Vol 65 (11) ◽  
pp. 685-693
Author(s):  
Martina Doubková ◽  
Jana Špeldová ◽  
Zita Chovancová

Author(s):  
T. B. Burmistrova

High-resolution computed tomography made it possible to assess changes in the lungs from the effects of industrial aerosols in the development of interstitial pulmonary diseases of professional and non-professional Genesis in 342 patients: pneumoconiosis, hypersensitive pneumonitis, allergic and fibrosing alveolitis, sarcoidosis, pulmonary tuberculosis. High-resolution computed tomography was an additional method in the diagnosis of various forms of lung diseases.


CHEST Journal ◽  
2018 ◽  
Vol 154 (4) ◽  
pp. 450A
Author(s):  
PAOLA FAVERIO ◽  
SILVIA GAMBERINI ◽  
LAURA CATTANEO ◽  
ALMERICO MARRUCHELLA ◽  
GIUSEPPE PACIOCCO ◽  
...  

1990 ◽  
Vol 25 (12) ◽  
pp. 1348 ◽  
Author(s):  
N. Asada ◽  
K. Doi ◽  
H. MacMahon ◽  
S. Montner ◽  
M. L. Giger ◽  
...  

2020 ◽  
Vol 30 (11) ◽  
pp. 6285-6292
Author(s):  
Ana Adriana Trusculescu ◽  
Diana Manolescu ◽  
Emanuela Tudorache ◽  
Cristian Oancea

Abstract Interstitial lung diseases are a diverse group of disorders that involve inflammation and fibrosis of interstitium, with clinical, radiological, and pathological overlapping features. These are an important cause of morbidity and mortality among lung diseases. This review describes computer-aided diagnosis systems centered on deep learning approaches that improve the diagnostic of interstitial lung diseases. We highlighted the challenges and the implementation of important daily practice, especially in the early diagnosis of idiopathic pulmonary fibrosis (IPF). Developing a convolutional neuronal network (CNN) that could be deployed on any computer station and be accessible to non-academic centers is the next frontier that needs to be crossed. In the future, early diagnosis of IPF should be possible. CNN might not only spare the human resources but also will reduce the costs spent on all the social and healthcare aspects of this deadly disease. Key Points • Deep learning algorithms are used in pattern recognition of different interstitial lung diseases. • High-resolution computed tomography plays a central role in the diagnosis and in the management of all interstitial lung diseases, especially fibrotic lung disease. • Developing an accessible algorithm that could be deployed on any computer station and be used in non-academic centers is the next frontier in the early diagnosis of idiopathic pulmonary fibrosis.


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