| chronic pancreatitis | Inflammatory disease of the pancreas characterised by fibrosis and irreversible loss of exocrine function. Chronic fibrosing pancreatitis, inflammation of the pancreas consisting of fibrosis, acinar atrophy, and calcification. Clinically, it follows a protracted course with relapses and remissions, and is usually due to alcohol abuse or malnutrition. Chronic relapsing pancreatitis, repeated exacerbations of pancreatitis in patient with chronic inflammation of that organ. Relapses are usually due to persistence of aetiologic factor or repeated exposure to it, such as occurs with partial ductal obstruction or chronic alcoholism. (05 Mar 2000) |
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| chronic pancreatitis: surgical treatment | <radiology> ERCP findings Surgical procedure, dilated proximal duct sphincterotomy, dilated distal duct distal pancreatectomy, with or without retrograde jejunal drainage, diffuse ductal dilatation Peustow procedure, (chain-of-lakes), sclerosed duct Child procedure (subtotal panc-x) (12 Dec 1998) |
| other-directed | Pertaining to a person readily influenced by the attitudes of others. (05 Mar 2000) |
| transferases (other substituted phosphate groups) | <enzyme> A class of enzymes that transfers substituted phosphate groups. Registry number: EC 2.7.8 (12 Dec 1998) |
| acute pancreatitis | <radiology> Findings: elevated hemidiaphragm, atelectasis / consolidation, pulmonary oedema (direct toxic effect? cardiosuppression?), pleural effusion (more common on left), sentinel loops, colon cut-off sign, antral pad, duodenum: widened loop, thickened folds, inverted 3 (Frostberg sign) (12 Dec 1998) |
| calcific pancreatitis | calcareous pancreatitis |
| pancreatitis | <gastroenterology, surgery> Acute or chronic inflammation of the pancreas, which may be asymptomatic or symptomatic and which is due to autodigestion of a pancreatic tissue by its own enzymes. It is caused most often by alcoholism or biliary tract disease, less commonly it may be associated with hyperlipaemia, hyperparathyroidism, abdominal trauma (accidental or operative injury), vasculitis or uraemia. (18 Nov 1997) |
| pancreatitis, acute necrotizing | Acute inflammation of the pancreas with areas of devitalised pancreatic and/or peripancreatic tissue. These necrotic areas may involve large areas of the pancreas or may be small. When a ct scan is performed with contrast media using a bolus technique, necrotic areas do not perfuse with media and are not enhanced. The lack of enhancement distinguishes necrotic tissue from the adjacent well-perfused viable pancreatic parenchyma. (12 Dec 1998) |
| pancreatitis, alcoholic | An acute or chronic degenerative and inflammatory lesion of the pancreas in the alcoholic which is potentially progressive or possibly reversible. (12 Dec 1998) |
| hereditary pancreatitis | <radiology> Rare, autosomal dominant, variable penetrance, onset often in childhood, on X-ray: large, round, peripherally dense calculi (12 Dec 1998) |
| anaemia of chronic disease | <disease> A form of anaemia which develops as the result of a long-term infection or illness. Chronic diseases can interfere with red blood cell production in addition to shortening red blood cell life span in the body. Symptoms are largely due to the underlying disease. Haemoglobin and haematocrit are generally low. Iron studies may be low to normal. Red blood cell indices may usually normal. (27 Sep 1997) |
| benign familial chronic pemphigus | Recurrent eruption of vesicles and bullae that become scaling and crusted lesions with vesicular borders, predominantly of the neck, groin, and axillary regions; autosomal dominant inheritance, presenting in late adolescence or early adult life. Synonym: Hailey-Hailey disease. (05 Mar 2000) |
| candidiasis, chronic mucocutaneous | A clinical syndrome characterised by development, usually in infancy or childhood, of a chronic, often widespread candidiasis of skin, nails, and mucous membranes. It may be secondary to one of the immunodeficiency syndromes, inherited as an autosomal recessive trait, or associated with defects in cell-mediated immunity, endocrine disorders, dental stomatitis, or malignancy. (12 Dec 1998) |
| granulomatous disease, chronic | A recessive x-linked defect of leukocyte function in which phagocytic cells ingest but fail to digest bacteria, resulting in recurring bacterial infections with granuloma formation. (12 Dec 1998) |
| persistent chronic hepatitis | A benign chronic hepatitis that may follow acute viral hepatitis A or B, or complicate bowel diseases; after six months, liver biopsy changes are mild, unlike active chronic hepatitis; rarely, if ever, progresses to cirrhosis, portal hypertension, or liver failure. (05 Mar 2000) |