Results 331 to 340 of about 672,015 (400)

Long‐term clinical course and outcome of interstitial pneumonia with autoimmune features

Respirology (Carlton South. Print), 2020
Idiopathic interstitial pneumonia (IIP) with autoimmune features that does not fulfil connective tissue disease (CTD) criteria has been recently defined as interstitial pneumonia with autoimmune features (IPAF). However, its long‐term clinical course and
H. Kim, Joo Hee Lee, E. Chae, Joon Seon Song, J. Song   +4 more
semanticscholar   +1 more source

Desquamative interstitial pneumonia

Histopathology, 2010
Tazelaar H D, Wright J L & Churg A
(2011)Histopathology 58, 509–516
Desquamative interstitial pneumoniaDesquamative interstitial pneumonia (DIP) is one of the rarest of the idiopathic interstitial pneumonias. It is characterized by the accumulation of macrophages in large numbers in the alveolar spaces associated with interstitial inflammation and ...
Henry D, Tazelaar, Joanne L, Wright, Andrew, Churg   +2 more
openaire   +2 more sources

Desquamative Interstitial Pneumonia

Chest, 1971
The pathologic features of desquamative interstitial pneumonia may be specific, but the x-ray changes are not. In most instances, a lung biopsy is essential for a definitive diagnosis. Evidence suggests that long-term prednisone therapy is effective in arresting or ameliorating the symptoms and pulmonary changes.
V E, Gould, T H, Gleason, L C, Winterscheid   +2 more
openaire   +4 more sources

Idiopathic interstitial pneumonias

Radiología (English Edition), 2012
The idiopathic interstitial pneumonias are diffuse lung diseases characterized by interstitial inflammation and fibrosis. High resolution computed tomography (HRCT) is the best imaging technique for the study of interstitial disease. The general term "idiopathic interstitial pneumonia" includes usual interstitial pneumonia/idiopathic pulmonary fibrosis,
T, Franquet, A, Giménez
openaire   +2 more sources

Interstitial pneumonia

Reactions Weekly, 2017
H. Spencer
openaire   +2 more sources

Desquamative Interstitial Pneumonia

Respiration, 1966
DIFFUSE or miliary lung diseases are being recognized and labeled with increasing frequency, often with considerable importance in relation to therapy. However, a large group of these disorders still remains unclassified. They are the chronic interstitial pneumonias, which, in the absence of familial history, collagen diseases, inhalation of noxious ...
A M, Goff, W F, McNary, E A, Gaensler
openaire   +3 more sources

Nonspecific Interstitial Pneumonia

Seminars in Respiratory and Critical Care Medicine, 2006
Nonspecific interstitial pneumonia (NSIP) describes a histopathologic pattern that can be seen in patients with immunodeficiency, drug or environmental exposures, and connective tissue diseases. The clinical diagnosis of NSIP, however, should be reserved for idiopathic cases in which no causative factor is identified.
Kevin R, Flaherty, Fernando J, Martinez
openaire   +2 more sources

Idiopathic Interstitial Pneumonias: Usual Interstitial Pneumonia versus Nonspecific Interstitial Pneumonia

Proceedings of the American Thoracic Society, 2006
Diffuse parenchymal lung diseases (DPLDs) are a group of disorders that involve the space between the epithelial and endothelial basement membranes. Recent guidelines for the classification of DPLDs recommended separating patients into several categories, including (1) DPLDs of known cause, (2) granulomatous DPLDs, (3) rare DPLDs with well-defined ...
openaire   +2 more sources

Idiopathic Interstitial Pneumonias

Journal of Thoracic Imaging, 2009
The idiopathic interstitial pneumonias (IIPs) are a group of diffuse parenchymal lung diseases of unknown etiology characterized by the presence of various degrees of inflammation and fibrosis. Confident definitive diagnosis of the various IIPs requires dynamic interaction among clinicians, radiologists, and pathologists to arrive at a clinico ...
C Isabela S, Silva, Nestor L, Müller
openaire   +2 more sources

Lymphoid Interstitial Pneumonia

Chest, 1972
Three cases of lymphoid interstitial pneumonia (LIP) are described. Lung biopsies demonstrated a similar characteristic histologic appearance of diffuse interstitial lymphocytes. Two had increased IgM. One patient developed a reticulum cell sarcoma. All were treated with prednisone but only one improved.
G M, Halprin, J, Ramirez, P C, Pratt
openaire   +2 more sources