Results 341 to 350 of about 672,015 (400)
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Interstitial Pneumonia

Essential Radiology Review, 2019
Rei Mitsuyama
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Desquamative interstitial pneumonia

British Journal of Diseases of the Chest, 1967
Summary The clinical, radiological and pathological features of desquamative interstitial pneumonia in a 55-year old Jamaican male negro are described. Although the patient presented with progressive effort dyspnœa there were minimal abnormal chest signs but marked derangement of the respiratory function tests.
V, Persaud   +3 more
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Idiopathic Interstitial Pneumonias

Seminars in Roentgenology, 2010
The idiopathic interstitial pneumonias are a distinct group of clinicopathologic entities. High-resolution computed tomography (HRCT) plays a critical role in the evaluation and management of patients. In the appropriate clinical setting, characteristic HRCT findings may be diagnostic, obviating the need for open lung biopsy.
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Usual Interstitial Pneumonia

Seminars in Respiratory and Critical Care Medicine, 2001
Usual interstitial pneumonia (UIP) is a distinct histological lesion observed in idiopathic pulmonary fibrosis (IPF), but can be found in other etiologies. The diagnosis of UIP can be established by surgical lung biopsy or by high resolution thin section computed tomographic scans (provided the radiographic features are classical).
Lynch, J. P. III   +6 more
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Acute interstitial pneumonia

European Respiratory Journal, 2000
The term "acute interstitial pneumonia" (AIP) describes an idiopathic clinicopathological condition, characterized clinically by an interstitial lung disease causing rapid onset of respiratory failure, which is distinguishable from the other more chronic forms of interstitial pneumonia.
D, Bouros   +3 more
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Lymphocytic Interstitial Pneumonia

Clinics in Chest Medicine, 1988
Lymphocytic interstitial pneumonia is a common complication of HIV infection in children, but uncommon in adults. It is characterized clinically by the presence of cough and dyspnea, diffuse pulmonary infiltrates on chest x-ray, restrictive pulmonary dysfunction, and hypoxemia. This constellation of findings usually erroneously suggests PCP, and a lung
A S, Teirstein, M J, Rosen
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Acute interstitial pneumonia

Clinics in Chest Medicine, 2004
The idiopathic interstitial pneumonias have unknown etiology and are characterized by diffuse parenchymal lung involvement and the potential to develop pulmonary fibrosis. Most portend a reduction in life expectancy due, in part, to the absence of effective therapies. The symptoms of idiopathic interstitial pneumonia develop insidiously.
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Usual Interstitial Pneumonia

Seminars in Respiratory and Critical Care Medicine, 2006
Usual interstitial pneumonia (UIP) is a distinct histological lesion observed in idiopathic pulmonary fibrosis (IPF) but can be found in other etiologies. The diagnosis of UIP can be established by surgical lung biopsy or by high-resolution thin-section computed tomographic (CT) scans (provided the radiographic features are classical).
Lynch, J. P. III   +4 more
openaire   +2 more sources

Idiopathic Bronchiolocentric Interstitial Pneumonia: A New Idiopathic Interstitial Pneumonia

Archivos de Bronconeumología ((English Edition)), 2007
Idiopathic interstitial pneumonias represent a diverse group of lung diseases with diffuse effects on the lung parenchyma. In 2002, the American Thoracic Society/European Respiratory Society consensus classification unified the descriptions of the different entities encompassed by idiopathic interstitial pneumonias.
Alejandro, Muñoz   +3 more
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Desquamative Interstitial Pneumonia

New England Journal of Medicine, 2023
Mohammed, Al-Halawani, Rachel K, Stevens
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