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Desquamative Interstitial Pneumonia
Respiration, 1966DIFFUSE 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 ...
Edward A. Gaensler +2 more
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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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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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Desquamative Interstitial Pneumonia
Chest, 1971The 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.
Victor E. Gould +2 more
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Idiopathic interstitial pneumonias
Radiología (English Edition), 2012The 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,
Tomás Franquet, Ana Giménez
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Desquamative interstitial pneumonia
Histopathology, 2010Tazelaar 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 ...
Andrew Churg +2 more
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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 ...
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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 ...
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Desquamative interstitial pneumonia
British Journal of Diseases of the Chest, 1967Summary 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.
Vasil Persaud +3 more
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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.
A C Nicholson +3 more
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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.
A C Nicholson +3 more
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Idiopathic Interstitial Pneumonias
Seminars in Roentgenology, 2010The 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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Lymphoid Interstitial Pneumonia
Chest, 1972Three 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.
Gerald M. Halprin +2 more
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