| IPH | idiopathic portal hypertension; idiopathic pulmonary hemosiderosis; idiopathic pulmonary hypertensio... |
|---|---|
| PACP | pulmonary alveolar-capillary permeability; pulmonary artery counterpulsation |
| PAGOD | pulmonary hypoplasia-hypoplasia of pulmonary artery-agonadism-omphalocele/diaphragmatic defect-dextr... |
| PAM | pancreatic acinar mass; penicillin aluminum monostearate; peptidylglycine alpha-amidating monooxygen... |
| PAP | pancreatitis-associated protein; Papanicolaou [test]; papaverine; passive-aggressive personality; pa... |
| illness, chronic | An illness that has persisted for a long period of time. It is a continuing disease process. (12 Dec 1998) |
|---|---|
| oesophageal stricture, chronic | A longstanding narrowing or closure of the normal opening of the swallowing tube leading to the stomach, usually caused by scarring by acid irritation. Narrowing of the oesophagus. A common complication of chronic gastroesophageal reflux disease (GERD). Severa procedures are available for stretching (dilating) the strictures without having to resort to surgery. One of the procedures involves placing a deflated balloon across the stricture at the time of endoscopy. The balloon is then inflated, thereby opening the narrowingcaused by the stricture. Another method involves inserting tapered dilators of different sizes through the mouth into the oesophagus to dilate the stricture. (12 Dec 1998) |
| ophthalmoplegia, chronic progressive external | One of the mitochondrial encephalomyopathies characterised by slowly progressive paralysis of the extraocular muscles. Muscle biopsies disclose the characteristic ragged red fibres and large numbers of mitochondria with deleted DNA. (12 Dec 1998) |
| jaundice, chronic idiopathic | A familial chronic form of nonhemolytic jaundice thought to be due to a defect in the excretion of conjugated bilirubin and certain other organic anions (e.g., sulfobromophthalein) by the liver. It is characterised by the presence of a brown, coarsely granular pigment in the hepatic cells, which is pathognomonic of the condition. (12 Dec 1998) |
| juvenile chronic arthritis | juvenile arthritis |
| juvenile chronic arthritis, systemic-onset | See: Juvenile rheumatoid arthritis, systemic-onset (still's disease). (12 Dec 1998) |
| kidney failure, chronic | An irreversible and usually progressive reduction in renal function in which both kidneys have been damaged by a variety of diseases to the extent that they are unable to adequately remove the metabolic products from the blood and regulate the body's electrolyte composition and acid-base balance. Chronic kidney failure requires haemodialysis or surgery, usually kidney transplantation. (12 Dec 1998) |
| fatigue syndrome, chronic | Syndrome of unknown cause, characterised by clinically evaluated, unexplained persistent or relapsing chronic fatigue of at least six months' duration which is not the result of ongoing exertion; is not substantially alleviated by rest; and results in substantial reduction of previous levels of occupational, educational, social, or personal activities. Common concurrent symptoms (of six months duration) include impairment of memory or concentration, diffuse pain, sore throat, tender lymph nodes, headaches of a new type, pattern, or severity, and unrefreshing sleep. The aetiology is suspected to be viral or immunologic. There are suggestions that chronic fatigue syndrome (sometimes called myalgic encephalomyelitis) may be identical to neurasthenia and fibromyalgia. (12 Dec 1998) |
| acute pulmonary alveolitis | Acute inflammation involving exudate into the pulmonary alveoli and impaired gas exchange; may result in necrosis with haemorrhage into the lungs; occurs in Goodpasture's syndrome, in association with a glomerulonephritis. (05 Mar 2000) |
| acute pulmonary eosinophilia | <chest medicine> A self-limiting inflammation in the lungs where there is associated infiltration of eosinophils into lung tissue. Chest X-ray reveals pulmonary infiltrates and full blood count shows increased numbers of eosinophils. The cause is unknown and the disease often resolves without treatment. Some forms may be treated with oral corticosteroids. Complications include restrictive cardiomyopathy due to fibrosis of the lining of the heart. (27 Sep 1997) |
| adenomatosis, pulmonary | A neoplastic disease in which the alveoli and distal bronchi are filled with mucus and mucus-secreting columnar epithelial cells. It is characterised by abundant, extremely tenacious sputum, chills, fever, cough, dyspnea, and pleuritic pain. (12 Dec 1998) |
| apical branch of inferior lobar branch of right pulmonary artery | <anatomy, artery> Branch (of the inferior lobar branch) of the right pulmonary artery serving the apical segment of the inferior lobe of the right lung. Synonym: ramus apicalis lobi inferioris arteriae pulmonalis dextrae. (05 Mar 2000) |
| apicoposterior branch of left superior pulmonary vein | <anatomy, vein> Drains apicoposterior bronchopulmonary segment of superior lobe of left lung. Synonym: ramus apicoposterior venae pulmonalis sinistrae superioris. (05 Mar 2000) |
| basal part of pulmonary artery | <anatomy, artery> See: right pulmonary artery, left pulmonary artery. (05 Mar 2000) |
| bifurcation of pulmonary trunk | The division of the pulmonary trunk into right and left pulmonary arteries. Synonym: bifurcatio trunci pulmonalis. (05 Mar 2000) |