| chronic pyelonephritis | Chronic inflammation of the renal parenchyma and pelvis resulting from bacterial infection, characterised by calyceal deformities and overlying large flat renal scars with patchy distribution. (05 Mar 2000) |
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| acute pyelonephritis | Acute inflammation of the renal parenchyma and pelvis characterised by small cortical abscesses and yellowish streaks in the medulla due to pus in the collecting tubules and interstitial tissue. (05 Mar 2000) |
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| ascending pyelonephritis | Pyelonephritis due to bacterial infection from the lower urinary tract, particularly by reflux of infected urine. (05 Mar 2000) |
| contagious bovine pyelonephritis | A specific necrotizing inflammation of the renal pelvis and ureters of cattle, caused by infection with Corynebacterium renale. (05 Mar 2000) |
| xanthogranulomatous pyelonephritis | <radiology> Big kidney, non-functioning (80%), dilated calyces, thin cortex, calculi (often staghorn), adult females, usually unilateral, Gram-negative infection, especially Proteus mirabilis, symptoms: fatigue, low fever, dysuria, flank pain, pathology: granulomata in parenchyma with foam cells, cholesterol slits, fibrosis, atrophic glomeruli, atypical focal form: may resemble focal carcinoma (12 Dec 1998) |
| pyelonephritis | <nephrology> Inflammation of the kidney and its pelvis, beginning in the interstitium and rapidly extending to involve the tubules, glomeruli and blood vessels, due to bacterial infection. (18 Nov 1997) |
| pyelonephritis, xanthogranulomatous | An inflammatory condition of the kidney most commonly resulting in a grossly enlarged and nonfunctioning kidney associated with stones and infection. (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) |
| chronic | Persisting over a long period of time. Origin: L. Chronicus, Gr. Chronos = time (18 Nov 1997) |
| chronic abscess | A long-standing collection of pus surrounded by fibrous tissue. (05 Mar 2000) |
| chronic absorptive arthritis | Arthritis accompanied by pronounced resorption of bone with shortening and deformity, especially of the hands; when the deformity is extreme, the condition has also been termed arthritis mutilans. (05 Mar 2000) |
| chronic acholuric jaundice | <haematology> A hereditary disorder that leads to a chronic haemolytic anaemia due to an abnormality in the red blood cell membrane. This disorder is caused by a defective gene. Red cells are resistant to stress and rupture easily. Infants may appear jaundiced and pale. Fatigue, weakness and shortness of breath are other symptoms that may be seen in older patients. The spleen may also be enlarged. Treatment includes splenectomy (removal of the spleen). After this is accomplished the life-span of the red blood cells returns to normal. (27 Sep 1997) |