eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | acute interstitial pneumonia |
| Comorbidity | C1279945|acute interstitial pneumonia |
| Sentences | 6 |
| PubMedID- 21189943 | acute interstitial pneumonia has been reported in 17 patients; usual interstitial pneumonia (uip) has been described in 2 individuals; 1 in 1991 and 1 in 2002; and desquamative interstitial pneumonia (dip) has been reported in 3 patients, 1 in 1989 and 2 in 2002. |
| PubMedID- 22754718 | acute interstitial pneumonia (aip), a rapidly progressive respiratory disease that affects patients with no pre-existing lung disease, is a lethal lung disease with a mortality rate of about 50%.1 unclassified interstitial pneumonia with fibrosis, which is not classified as a disease entity under the classification of interstitial lung diseases in adults,1 shows clinical and radiological findings that are similar with those of aip. |
| PubMedID- 22853774 | Aip: acute interstitial pneumonia; ats: american thoracic society; cop: cryptogenic organizing pneumonia; cxr: chest x-ray; dip: desquamative interstitial pneumonia; dlco: diffusing capacity of the lung for carbon monoxide; ers: european respiratory society; fvc: forced vital capacity; fev: forced expiratory volume in one second; fpf: familial pulmonary fibrosis; fpf-dc: familial pulmonary fibrosis - diagnosed clinically; fpf-ds: familial pulmonary fibrosis - diagnosed through family screening; hrct: high resolution computed tomography; iip: idiopathic interstitial pneumonias; ild: interstitial lung disease; ipf: idiopathic pulmonary fibrosis; lip: lymphocytic interstitial pneumonia; nl: newfoundland and labrador, canada; nsip: non-specific interstitial pneumonitis; omim: online mendelian inheritance in man; pf: pulmonary fibrosis; pft: pulmonary function test; rb-ild: respiratory bronchiolitis-associated interstitial lung disease; sd: standard deviation; sftpc: surfactant protein c; sftpa2: surfactant protein a2; tert: telomerase reverse transcriptase; terc: telomerase rna component; uip: usual interstitial pneumonitis. |
| PubMedID- 23227081 | The causes for dad are numerous, but the chief cause is acute interstitial pneumonia or acute exacerbation of idiopathic interstitial pneumonia, in cases of idiopathic manifestation. |
| PubMedID- 24586910 | Dm-a/sip: acute/subacute interstitial pneumonia in dermatomyositis. |
| PubMedID- 21687544 | acute interstitial pneumonia (aip) or hamman rich syndrome is a rare and fulminant form of lung injury, originally described by hamman and rich in 1935 [1]. |
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