| AA | 1) Aortic Arch(= Arcus Aortae)(= AA); 대동맥궁 2) Aplastic Anemia - Anemia |
|---|---|
| AEF | Amyloid Enhancing Factor |
| AH | 1) Atrial Hypertrophy 2) Anti-Hyaluronidase 3) Amyloid imm... |
| AL | Amyloid immunoglobulin Light chain protein |
| AP | 1) Alkaline Phosphatase = ALP 2) Amyloid Plasm... |
| amyloid tumour | A localised form of amyloidosis in which amyloid occurs as masses or nodules beneath the skin or mucous membranes, e.g., in the larynx. Synonym: amyloid tumour, focal amyloidosis. (05 Mar 2000) |
|---|---|
| beta-amyloid | <protein> The protein which forms thick deposits, or plaques, in the brains of people with Alzheimer's disease, a disease where memory skills gradually deteriorate with age. (13 Nov 1997) |
| cerebral amyloid angiopathy | <pathology> A condition where there is a deposition of amyloid (insoluble protein) in the walls of the arteries which supply the brain. This results in an increased risk of dementia and-or intracerebral haemorrhage. Cerebral amyloidosis or cerebral amyloid angiopathy, is a complication of primary amyloidosis. Origin: Gr. Pathos = disease (27 Sep 1997) |
| serum amyloid | In secondary amyloidosis the fibrils deposited in tissues are unrelated to immunoglobulin light chains (in contrast to the situation in primary amyloidosis) and are made of amyloid A protein (AA protein). This is derived from serum amyloid A (SAA) that is the apolipoprotein of a high density lipoprotein and an acute phase protein. Partial proteolysis converts SAA into the pleated sheet configuration of the amyloid fibrils. Amyloid P protein is also found as a minor component of the fibrils (in both primary and secondary amyloidosis) and is derived from serum amyloid P that has similarity to C-reactive protein. The physiological role remains obscure. (18 Nov 1997) |
| serum amyloid P component | Precursor of amyloid component P, found in basement membrane. Member of the pentraxin family. See: serum amyloid. (18 Nov 1997) |
| islet amyloid peptide | <hormone, protein> Peptide of 37 amino acids that selectively inhibits insulin stimulated glucose uptake in muscle. Structurally related to calcitonin gene-related peptide. (15 Oct 1997) |
| familial amyloid neuropathy | <neurology> A disorder in which various peripheral nerves are infiltrated with amyloid and their functions disturbed, an abnormal prealbumin is also formed and is present in the blood; characteristically, it begins during mid-life and is found largely in persons of Portuguese descent. Other rare clinical types occur. Inheritance: autosomal dominant. Synonym: familial amyloidosis, hereditary amyloidosis. (05 Mar 2000) |
| alcoholic hyaline bodies | Large, poorly defined accumulations of eosinophilic material in the cytoplasm of damaged hepatic cells in certain forms of cirrhosis and marked fatty change especially due to alcoholism. Synonym: alcoholic hyalin, alcoholic hyaline bodies. (05 Mar 2000) |
| Alder bodies | Granular inclusions in polymorphonuclear leukocytes; they take on a dark colour with Giemsa-Wright stain and react metachromatically with toluidine blue. See: Alder's anomaly. (05 Mar 2000) |
| aortic bodies | Small clusters of chemoreceptive and supporting cells located near the aortic arch, the pulmonary arteries, and the coronary arteries. The aortic bodies sense pH, carbon dioxide, and oxygen concentrations in the blood and participate in the control of respiration. (12 Dec 1998) |
| Arnold's bodies | Small portions or minute fragments of erythrocytes (sometimes mistaken for blood platelets), or small "ghosts" of erythrocytes. (05 Mar 2000) |
| asbestos bodies | Ferruginous body's with asbestos fibres as a core; a histologic hallmark of exposure to asbestos. (05 Mar 2000) |
| Aschoff bodies | <pathology> Small granulomas composed of macrophages, lymphocytes and multinucleate cells grouped around eosinophilic hyaline material derived from collagen. Characteristic of the myocarditis of rheumatic fever. (18 Nov 1997) |
| Auer bodies | Rod-shaped structures of uncertain nature in the cytoplasm of immature myeloid cells, especially myeloblasts, in acute myelocytic leukaemia; may be an abnormal form of lysosomes; they contain peroxidase and acid phosphatase, and stain red by azure-eosin stains. Synonym: Auer rods. (05 Mar 2000) |
| Babes-Ernst bodies | Intracellular granules, present in many species of bacteria, which possess a strong affinity for nuclear stains. (05 Mar 2000) |