| 영문 | purpura | 한글 | 자색반증 |
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| 설명 | 피부내의 출혈로 인하여, 피부 표피를 통하여 쉽게 보이는 자홍색 혹은 적갈색 반점을 특징으로 하는 일련의 질환을 총칭하는 용어이다. 대개 홍반과 구별해야 하는 데 홍반은 피부밑의 혈관이 팽창하여 붉게 보이는 현상으로 투명한 자를 이용하여 피부를 눌러서 관찰해보면 쉽게 구별이 가능하다. 이때 홍반은 붉은 색이 없어지지만, 자반은 붉은 색이 없어지지 않는다. |
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| ITP | idiopathic thrombocytopenic purpura; immune thrombocytopenia; immunogenic thrombocytopenic purpura; ... |
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| TTP | Thrombotic Thrombocytopenic Purpura |
| TTP | thiamine triphosphate; thrombotic thrombocytopenic purpura; thymidine triphosphate; time to peak; tr... |
| ATP | 1) Adenosine Tri-Phosphate 2) Autoimmune Thrombocytopenic Purpura |
| ITP | Idiopathic(Immune) Thrombocytopenic Purpura |
| TTP | Thrombotic Thrombocytopenic Purpura |
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| TTP-HUS | Thrombotic thrombocytopenic purpura-hemolytic uremic syndrome |
| AITP | Autoimmune thrombocytopenic purpura |
| ATP | Autoimmune thrombocytopenic purpura |
| ITP | Idiopathic thrombocytopenic purpura |
| thrombotic thrombocytopenic purpura | A rapidly fatal or occasionally protracted disease with varied symptoms in addition to purpura, including signs of central nervous system involvement, due to formation of fibrin or platelet thrombi in arterioles and capillaries in many organs. Synonym: Moschcowitz' disease. (05 Mar 2000) |
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| purpura, thrombotic thrombocytopenic | A disease characterised by thrombocytopenia, haemolytic anaemia, bizarre neurological manifestations, azotemia, fever, and thromboses in terminal arterioles and capillaries. (12 Dec 1998) |
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| purpura, thrombocytopenic | Any form of purpura in which the platelet count is decreased. Many forms are thought to be caused by immunological mechanisms. (12 Dec 1998) |
| purpura, thrombocytopenic, idiopathic | Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IgG autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms. (12 Dec 1998) |
| idiopathic thrombocytopenic purpura | <haematology> A rare autoimmune disorder characterised by an acute shortage of platelets with resultant bruising and spontaneous bleeding. The platelet count becomes exceedingly low and spontaneous bleeding from the gums, gastrointestinal tract and nose can be seen. Physical examination may demonstrate enlargement of the spleen. A typical rash occurs to do microscopic haemorrhage of small blood vessels in the skin. Platelet counts under 10,000 can lead to spontaneous haemorrhage into the brain causing death. Treatment with corticosteroids is generally effective. Surgical removal of the spleen (splenectomy) is reserved for some patients. Anti-platelet antibodies are detectable in some cases. It may present in either an acute or a chronic form. Acronym: ITP (20 Sep 2002) |
| immune thrombocytopenic purpura | <haematology> A low number of platelets in the blood, which is common in people with HIV, but often resolves as immune deficiency worsens. HIV-related ITP usually does not have serious consequences. Its cause has not been definitely determined. Treatment with AZT frequently alleviates the condition. (09 Oct 1997) |
| thrombocytopenic purpura | See: idiopathic thrombocytopenic purpura. (05 Mar 2000) |
| abacterial thrombotic endocarditis | Verrucous endocardial lesions occurring in the terminal stages of many chronic infectious and wasting diseases. Synonym: abacterial thrombotic endocarditis, cachectic endocarditis, terminal endocarditis, thromboendocarditis. (05 Mar 2000) |
| nonbacterial thrombotic endocarditis | Verrucous endocardial lesions occurring in the terminal stages of many chronic infectious and wasting diseases. Synonym: abacterial thrombotic endocarditis, cachectic endocarditis, terminal endocarditis, thromboendocarditis. (05 Mar 2000) |
| thrombotic | Relating to, caused by, or characterised by thrombosis. (05 Mar 2000) |
| thrombotic disease due to protein c deficiency | Protein C is a protein in plasma that enters into the cascade of biochemical events leading to the formation of a clot. Deficiency of protein c results in thrombotic (clotting) disease and excess platelets with recurrent thrombophlebitis (inflammation of the vein that occurs when a clot forms). The clot can break loose and travel through the blood stream (thromboembolism) to the lungs causing a pulmonary embolism, brain causing a stroke (cerebrovascular accident), heart causing an early heart attack, skin causing what in the newborn is called neonatal purpura fulminans, the adrenal gland causing haemorrhage with abdominal pain, abnormally low blood pressure (hypotension), and salt loss. Protein c deficiency is due to possession of one gene (heterozygosity) in chromosome band 2q13-14. The possession of two such genes (homozygosity) is usually lethal. (12 Dec 1998) |
| thrombotic gangrene | Gangrene due to occlusion of an artery by a thrombus. (05 Mar 2000) |
| thrombotic hydrocephalus | Increase in cerebrospinal fluid and of intracranial pressure following thrombosis of the cerebral veins or sinuses; caused by septic infection, dehydration, tuberculosis, typhoid, leukaemia, and other conditions. (05 Mar 2000) |
| thrombotic infarct | An infarct caused by a thrombus. (05 Mar 2000) |
| thrombotic microangiopathy | Thrombosis within small blood vessels, as in thrombotic thrombocytopenic purpura. (05 Mar 2000) |
| thrombotic phlegmasia | An extreme edematous swelling of the leg following childbirth, due to thrombosis of the iliofemoral veins. Synonym: leukophlegmasia dolens, milk leg, puerperal phlebitis, thrombotic phlegmasia, white leg. (05 Mar 2000) |
| thrombotic thrombocytopenic purpura |
A disease state in which red blood cells and platelets are destroyed and the body produces excessive blood clots which may damage the kidneys and nervous system.
출처: www.cbcsf.org/pages/glossary/
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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