| pulmonary veins | The veins that return the oxygenated blood from the lungs to the left atrium of the heart. (12 Dec 1998) |
|---|---|
| pulmonary venolobar syndrome | <radiology> Always involves aplasia of one or more lobes of right lung, variably involves: partial anomalous pulmonary venous return (scimitar-shaped vein), usually drains to IVC; but portal vein, hepatic vein, RA possible, absent or small pulmonary artery perfusing abnormal lung segment, arterial supply from thoracic/abdominal aorta or coeliac axis, anomalies of hemidiaphragm on affected side, anomalies of bony thorax or thoracic soft tissues Synonym: scimitar syndrome (12 Dec 1998) |
| pulmonary veno-occlusive disease | Obstruction of the small- and medium-sized pulmonary veins by fibrous proliferation of the intima and media or by thrombosis or a combination of both. (12 Dec 1998) |
| pulmonary ventilation | The process of exchange of air between the lungs and the ambient air. Pulmonary ventilation is a measure of the rate of ventilation expressed usually in liters per minute. (12 Dec 1998) |
| pulmonary wedge pressure | The blood pressure as recorded after wedging a catheter in a small pulmonary artery; believed to reflect the pressure in the pulmonary capillaries. (12 Dec 1998) |
| simple pulmonary eosinophilia | Pulmonary infiltrates seen as transient migratory shadows on the chest X-ray, accompanied by blood eosinophilia; often symptomless, but there may be cough, fever, and breathlessness; most cases are due to worm infestation, especially by Ascaris lumbricoides; a few cases follow administration of drugs. Synonym: Loffler's syndrome. (05 Mar 2000) |
| hypertension, pulmonary | High blood pressure in the pulmonary arteries. Normally, the pressure in the pulmonary arteries is low (compared to that in the aorta). Pulmonary hypertension can irrevocably damage the lungs. Pulmonary hypertension is made up of pulmonary for lung, hyper for high, and tension for blood pressure. (in french, the word for blood pressure is tension ). (12 Dec 1998) |
| neonatal pulmonary venous hypertension | <radiology> With cardiomegaly, hypoplastic left heart, critical aortic stenosis, cor triatriatum, pulmonary venous atresia, normal heart size, infradiaphragmatic TAPVR (12 Dec 1998) |
| superior branch of the right and left inferior pulmonary veins | Tributaries of the right and left inferior pulmonary veins which receive oxygenated blood from the superior [S6] bronchopulmonary segments of the inferior lobes of the right and left lungs. Synonym: ramus superior venae pulmonalis dextrae/sinistrae inferioris. (05 Mar 2000) |
| superior lingular branch of lingular branch of superior lobar left pulmonary artery | <anatomy, artery> Branch (of the lingular branch) of the left pulmonary artery serving the superior lingular segment of the superior lobe of the left lung. Synonym: ramus lingularis superior. (05 Mar 2000) |
| superior part of lingular branch of left pulmonary vein | <anatomy, vein> The vein that drains the superior lingular bronchopulmonary segment of the left lung. Synonym: pars superior rami lingularis venae pulmonis sinistri. (05 Mar 2000) |
| superior pulmonary sulcus tumour | <oncology, tumour> Tumour originating from the superior sulcus of the lung that invades all or a portion of the brachial plexus. (16 Dec 1997) |
| diffuse interstitial pulmonary fibrosis | This represents a group of pulmonary disorders (lower respiratory tract) that leads to a functional loss in the alveolar air sacs and a compromise in the diffusion of oxygen from air to blood. There is widespread inflammation and scar tissue (fibrosis) formation within the lung. The causes are varied and include: inorganic and organic dusts, gases, fumes, vapors, infections, radiation, medications, coal dust, silicosis and byssinosis. When the cause is not identifiable it is referred to as idiopathic diffuse interstitial pulmonary fibrosis (27 Sep 1997) |
| diffuse pulmonary haemorrhage | <radiology> Thrombocytopenia, coagulopathy, idiopathic pulmonary haemosiderosis, Goodpasture syndrome, systemic lupus erythematosus, Wegeners granulomatosis, polyarteritis nodosa, Henoch-Schonlein purpura, Behcet disease, D-penicillamine, lymphangiography (12 Dec 1998) |
| idiopathic pulmonary fibrosis | <radiology> Aka: usual interstitial pneumonia (UIP), 5-6th decade; M:F = 1:1, clubbing of fingers (83%), lymphocytosis on lavage, increased occurence of bronchogenic CA, average survival of 4-6 years; 87% mortality CXR findings: occasional ground glass pattern in early stage of alveolitis, diffuse reticulations (60%) predominantly at bases, honeycombing, pleural effusion (4%); pleural thickening (6%), pneumothorax in 7% (late stage), progressive volume loss see: interstitial pulmonary fibrosis (12 Dec 1998) |