| GC(T)A | giant cell (temporal) arteritis |
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| HA | H antigen; Hakim-Adams [syndrome]; halothane anesthesia; Hartley [guinea pig]; headache; health alli... |
| JRA | Juvenile Rheumatoid Arthritis; ¿¬¼Ò±â ·ù¸¶ÅäÀÌµå °üÀý¿° = Juvenile Chronic Arthritis; ¿¬¼Ò±â ¸¸¼º °üÀý... |
| RA | 1) Refractory Anemia 2) Rheumatoid Arthritis ? Arthritis 3... |
| CRA | central retinal artery; Chinese restaurant asthma; chronic rheumatoid arthritis; constant relative a... |
| juvenile rheumatoid arthritis | <pathology> Juvenile rheumatoid arthritis (JRA) is a form of rheumatoid arthritis in children that generally occurs prior to age 16. In contrast with the adult type, a fever is more pronounced. Cardiac involvement with pericarditis is more common. The arthritis favors one or more large joints and can interfere with normal bone growth. A positive rheumatoid factor is seen more uncommonly in this form of arthritis. Treatment is similar to the adult form of the disease. Up to 75% recover with treatment. Less than 10% are severely disabled by JRA. (27 Sep 1997) |
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| juvenile rheumatoid arthritis, systemic-onset | Also known as systemic-onset juvenile chronic arthritis. Still's disease presents with systemic (bodywide) illness including high intermittent fever, a salmon-coloured skin rash, swollen lymph glands, enlargement of the liver and spleen, and inflammation of the lungs (pleuritis) and around the heart (pericarditis). The arthritis may not be immediately apparent but it does always surface and it may persists long after the systemic symptoms are gone. (12 Dec 1998) |
| factor, rheumatoid | Rheumatoid factor is an antibody that is measurable in the blood. It is commonly used as a blood test for the diagnosis of rheumatoid arthritis. Rheumatoid factor is present in about 80% of adults (but a much lower proportion of children) with rheumatoid arthritis. It is also present in patients with other connective tissue diseases (such as systemic lupus erythematosus) and in some with infectious diseases (such as infectious hepatitis). (12 Dec 1998) |
| arteritis | <pathology> Inflammation of an artery. See: cranial arteritis, giant cell arteritis. (20 Jun 2000) |
| arteritis nodosa | <radiology> Necrotizing vasculitis of medium-sized arteries, usually in male adults, associated with hepatitis B antigen, kidney: most frquently involved organ (85%), multiple small intrarenal aneurysms, aneurysms may disappear (thrombosis) or appear in new locations, arterial narrowing and thrombosis (chronic/healing stage), multiple small cortical infarcts, associated with hypertension and renal failure, chest involvement (70%), cardiomegaly/pericardial effusion (14%), wedge shaped/round peripheral infiltrates simulating PE (14%), interstitial lower lung field pneumonitis, also may involve liver (66%), mesenteric vessels (50%), skeletal muscle (39%), skin (20%) (12 Dec 1998) |
| arteritis obliterans | Obliterating endarteritis, an extreme degree of endarteritis proliferans closing the lumen of the artery. Synonym: arteritis obliterans, obliterating arteritis. (05 Mar 2000) |
| arteritis virus | A genus that is currently unclassified, arterivirus is likely to be part of coronaviridae or a new family. It was previously classified under togaviridae. The type species is arteritis virus, equine. (12 Dec 1998) |
| brachiocephalic arteritis | Giant-cell arteritis seen in older adults; characterised by inflammatory lesions in medium sized arteries, most commonly in the head, neck and/or shoulder girdle area; lesions include fragmented elastin, macrophages, and giant cells. Erythrocyte sedimentation rate is usually markedly elevated. Visual loss can occur. (05 Mar 2000) |
| giant cell arteritis | <pathology> An inflammatory condition of the temporal artery. It is a serious chronic vascular disease, characterised by inflammation of the walls of the blood vessels (vasculitis). The age of affected patients is usually over 50 years of age. It most often involves the carotid artery system, and can lead to blindness or stroke. It can be diagnosed by biopsy of an artery, but there is often a false negative result. Elevation of the erythrocyte sedimentation rate is typical. Treatment is with high dose steroids. Common symptoms include headaches and tenderness over the temple (temporal artery). Can be associated with polymyalgia rheumatica. See: polymyalgia rheumatica. Synonym: cranial arteritis, temporal arteritis (20 Jun 2000) |
| rheumatic arteritis | Arteritis due to rheumatic fever; Aschoff bodies are frequently found in the adventitia of small arteries, especially in the myocardium, and may lead to fibrosis and constriction of the lumens. (05 Mar 2000) |
| granulomatous arteritis | giant cell arteritis |
| coronary arteritis | Inflammation of any or all of the layers of coronary artery walls. (05 Mar 2000) |
| cranial arteritis | <pathology> An inflammatory condition of the temporal artery. It is a serious chronic vascular disease, characterised by inflammation of the walls of the blood vessels (vasculitis). The age of affected patients is usually over 50 years of age. It most often involves the carotid artery system, and can lead to blindness or stroke. It can be diagnosed by biopsy of an artery, but there is often a false negative result. Elevation of the erythrocyte sedimentation rate is typical. Treatment is with high dose steroids. Common symptoms include headaches and tenderness over the temple (temporal artery). Can be associated with polymyalgia rheumatica. See: polymyalgia rheumatica. Synonym: cranial arteritis, temporal arteritis (20 Jun 2000) |
| Heubner's arteritis | Inflammation of arteries within the circle of Willis secondary to chronic basal meningitis from tubercle bacillus or particular fungi such as Cryptococcus, Histoplasma, or Coccidiodes. (05 Mar 2000) |
| Horton's arteritis | giant cell arteritis |
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