نتایج جستجو برای: interstitial lung disease

تعداد نتایج: 1739449  

Journal: :Reumatologia clinica 2015
Renzo Pérez-Dórame Mayra Mejía Heidegger Mateos-Toledo Jorge Rojas-Serrano

OBJECTIVE To describe the association between rheumatoid arthritis disease activity (RA) and interstitial lung damage (inflammation and fibrosis), in a group of patients with rheumatoid arthritis-associated interstitial lung disease (RA-ILD). METHODS A retrospective study of RA patients with interstitial lung disease (restrictive pattern in lung function tests and evidence of interstitial lun...

Journal: :The New England journal of medicine 2011
George R Washko Gary M Hunninghake Isis E Fernandez Mizuki Nishino Yuka Okajima Tsuneo Yamashiro James C Ross Raúl San José Estépar David A Lynch John M Brehm Katherine P Andriole Alejandro A Diaz Ramin Khorasani Katherine D'Aco Frank C Sciurba Edwin K Silverman Hiroto Hatabu Ivan O Rosas

BACKGROUND Cigarette smoking is associated with emphysema and radiographic interstitial lung abnormalities. The degree to which interstitial lung abnormalities are associated with reduced total lung capacity and the extent of emphysema is not known. METHODS We looked for interstitial lung abnormalities in 2416 (96%) of 2508 high-resolution computed tomographic (HRCT) scans of the lung obtaine...

Journal: :The European respiratory journal 2003
S Veeraraghavan P I Latsi A U Wells P Pantelidis A G Nicholson T V Colby P L Haslam E A Renzoni R M du Bois

Idiopathic pulmonary fibrosis (IPF), which has the histological pattern of usual interstitial pneumonia (UIP), is a progressive interstitial lung disease with a poor prognosis. Idiopathic interstitial pneumonias with a histological pattern of nonspecific interstitial pneumonia (NSIP) have a better prognosis than UIP, and may present with a clinical picture identical to IPF. The authors hypothes...

Journal: :European Journal of Cardio-Thoracic Surgery 2002

2015
Ellen De Langhe Jan Lenaerts Xavier Bossuyt Rene Westhovens Wim A Wuyts

INTRODUCTION Interstitial lung disease can be idiopathic or occur in the setting of connective tissue diseases. In the latter case it requires a different treatment approach with a better prognosis. Interstitial lung disease can precede the onset of typical connective tissue disease features by many years, and therefore meticulous multidisciplinary follow-up is crucial. This case highlights the...

2014
Yoshiki YAMAYA Kazuyuki SUZUKI Toshihiro WATARI Ryuji ASANO

We measured bronchoalveolar lavage fluid (BALF) and serum canine surfactant protein (cSP)-A concentrations in dogs with chronic cough. There were no significant differences between bronchial and interstitial lung diseases in BALF cSP-A concentrations. However, serum cSP-A concentrations in dogs with the interstitial lung disease as diffuse panbronchiolitis and idiopathic pulmonary fibrosis were...

Journal: :European respiratory review : an official journal of the European Respiratory Society 2017
Marios Panagiotou Alistair C Church Martin K Johnson Andrew J Peacock

Pulmonary vascular and cardiac impairment is increasingly appreciated as a major adverse factor in the natural history of interstitial lung disease. This clinically orientated review focuses on the current concepts in the pathogenesis, pathophysiology and implications of the detrimental sequence of increased pulmonary vascular resistance, pre-capillary pulmonary hypertension and right heart fai...

Journal: :Thorax 2008
M L Doan R P Guillerman M K Dishop L M Nogee C Langston G B Mallory M M Sockrider L L Fan

BACKGROUND Mutations in the ABCA3 gene can result in fatal surfactant deficiency in term newborn infants and chronic interstitial lung disease in older children. Previous studies on ABCA3 mutations have focused primarily on the genetic abnormalities and reported limited clinical information about the resultant disease. A study was undertaken to analyse systematically the clinical presentation, ...

Journal: :International journal of clinical and experimental medicine 2014
Yihua Lin Qun Yi Deyun Cheng

Primary Sjögren's syndrome is a chronic inflammatory disorder with many extraglandular organ systems involved, including the lungs. Diffuse interstitial lung disease is the most serious form of lung involvement. Parenchymal lung involvement in primary Sjögren's syndrome is usually manifested by cough and/or slowly progressive dyspnea and most of the cases present as chronic course. We describe ...

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