| 영문 | transient ischemic attack(TIA) | 한글 | 일과성허혈발작 |
|---|---|---|---|
| 설명 | 뇌혈관 폐쇄에 의한 일과성의 실신, 두통, 시력상실 등의 증세를 보이는 상태로 24시간 이내에 모든 증상이 회복되는 경우를 말한다. 후에 영구적인 뇌허혈 즉 뇌경색증이 올 가능성이 매우 높아진다. |
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| 영문 | red bone marrow | 한글 | 적색골수 |
|---|---|---|---|
| 설명 | 분화중의 갈비뼈, 척추뼈나 그 외의 많은 작은 뼈에 있는 활동성 골수이다. 적혈구나 과립백혈구의 생산 장소이다. |
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| 영문 | acquired immunodeficiency syndrome | 한글 | 후천면역결핍증후군, 에이즈 |
|---|---|---|---|
| 설명 | 인간면역결핍바이러스(HIV)에 의하여 면역 세포가 파괴됨으로써 인체의 면역능력이 극도로 저하되어 병원체에 대하여 무방비 상태에 이르는 병. 에이즈 바이러스의 감염으로 생기며, 1981년 미국에서 처음 보고되었다. 최초 감염으로부터 증상이 나타나기까지는 평균 10년 정도 걸리며 사망률이 대단히 높다. 성적 접촉, 오염 주사기 사용, 오염 혈액 및 혈액 제제 사용, 에이즈 산모로부터 수직감염 따위에 의하여 감염된다. 감염 후 일과성으로 감기와 같은 증상을 보이며 바이러스혈증으로 되지만 바이러스는 감소되고 6~8주 후에는 항체가 양성으로 된다. 6~10년 정도의 무증후성 보균기간을 지나서 에이즈관련증후군(AIDS related syndrome)으로 된다. 저항력의 감소, 림프절비대, 체중감소, 발열, 만성설사가 이어진다. 그 후 에이즈로 되며, 폐포자충폐렴 등의 원충병, 칸디다 등의 진균증, 헤르페스바이러스군 등의 기회감염이 이어진다. 또한 카포시육종, 림프종 등을 병발해서 사망한다. 바이러스의 뇌조직내 증식으로 치매를 일으킬 수도 있다. HIV-1은 10년간에 사망률이 90%, HIV-2는 10%이다. |
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| 영문 | white blood cell(WBC), leukocyte | 한글 | 백혈구 |
|---|---|---|---|
| 설명 | 혈액내에 골수구계세포와 림프계세포, 단핵구계세포를 모두 통틀어 말한다. 백혈구의 증가가 있으면 대개 감염이 있거나, 혹은 탈수현상이 있음을 의미한다. 또한 지나친 백혈구수의 감소는 인체내 면역기능이 떨어져 있음을 의미하며, 다른 질병에 의해 나타나는 이차적인 현상이 아닌지 꼭 진단을 받아보아야 한다. |
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| CAPRCA | chronic, acquired, pure red cell aplasia |
|---|---|
| PRCA | Pure Red Cell Aplasia |
| CPRCA | constitutional pure red cell aplasia |
| PRCA | pure red cell aplasia |
| RC | an electronic circuit containing a resistor and capacitor in series; radiocarpal; reaction center; r... |
| PRCA | Pure Red Cell Aplasia |
|---|---|
| ACC | Aplasia cutis congenita |
| CP | Commercially pure |
| CP Ti | Commercially pure titanium |
| IUPAC | International Union of Pure and Applied Chemistry |
| red-cell aplasia, pure | Suppression of erythropoiesis with little or no abnormality of leukocyte or platelet production. (12 Dec 1998) |
|---|---|
| pure red cell aplasia | A transitory arrest of red blood cell production which may occur in the course of a haemolytic anaemia, often preceded by infection, or as a complication of certain drugs; if the arrest persists anaemia may result. See: congenital hypoplastic anaemia. (05 Mar 2000) |
| pure red cell anaemia | Congenital nonregenerative, familial hypoplastic, or pure red cell anaemia; erythrogenesis imperfecta; Diamond-Blackfan syndrome; autosomal recessive normocytic normochromic anaemia resulting from congenital hypoplasia of the bone marrow, which is grossly deficient in erythroid precursors while other elements are normal; anaemia is progressive and severe, but leukocyte and platelet counts are normal or slightly reduced; survival of transfused erythrocytes is normal; minor congenital anomalies are found in some patients. Synonym: congenital nonregenerative anaemia, Diamond-Blackfan anaemia, Diamond-Blackfan syndrome, erythrogenesis imperfecta, familial hypoplastic anaemia, pure red cell anaemia. (05 Mar 2000) |
| aplasia | <embryology> A lack of development of an organ or tissue or of the cellular products from an organ or tissue. Compare: hypoplasia. Origin: Gr. Plassein = to form (18 Nov 1997) |
| aplasia cutis congenita | Congenital absence or deficiency of a localised area of skin, with the base of the defect covered by a thin translucent membrane; most often a single area near the vertex of the scalp, but may occur in other areas; underlying structures may also be affected; autosomal inheritance, either dominant or recessive. (05 Mar 2000) |
| radial aplasia-thrombocytopenia syndrome | <syndrome> Aplasia (absence) of the radius (the long bone on the thumb-side of the forearm) and thrombocytopenia (low blood platelets) are key features characterizing this syndrome. There is phocomelia (flipper-limb) with the thumbs always present. The fibula (the smaller bone in the lower leg) is often absent. The risk of bleeding from too few platelets is high in early infancy but lessens with age. The condition is inherited in an autosomal recessive trait with one gene (on a non-sex chromosome) coming from each parent to the child affected with the disease. Alternative names include thrombocytopenia-absent radius syndrome, tar syndrome, and tetraphocomelia-thrombocytopenia syndrome. (12 Dec 1998) |
| germinal aplasia | A disorder in which the seminiferous tubules exhibit an abnormal cytoarchitecture and extensive hyalinization; the testes are small, and few spermatozoa are formed; the body habitus may be eunuchoid, and gynaecomastia may be present; urinary gonadotropin output is usually high, and the incidence of mental deficiency and illness increased; sex chromatin may be male or female, and androgen secretion ranges from subnormal to normal. It is a constant feature of (and is often used synonymously with) Klinefelter's syndrome. Synonym: germinal aplasia. (05 Mar 2000) |
| gonadal aplasia | Congenital absence of essentially all gonadal tissue; the external genitalia and genital ducts are female, but if interstitial cells of Leydig are present, the external genitalia are commonly ambiguous and the genital ducts are female. See: gonadal dysgenesis. Compare: Klinefelter's syndrome, Turner's syndrome. Synonym: gonadal agenesis. (05 Mar 2000) |
| congenital aplasia of thymus | diGeorge syndrome |
| syndrome, radial aplasia-thrombocytopenia | See syndrome, tar. (12 Dec 1998) |
| thymic aplasia | <disease, immunology> A lack of T lymphocytes, due to failure of the thymus to develop, resulting in very reduced cell-mediated immunity though serum immunoglobulin levels may be normal. See: DiGeorge syndrome. Origin: Gr. Plassein = to form (18 Nov 1997) |
| cerebral ischemia, transient | Nonconvulsive, reversible, focal neurologic deficits lasting minutes up to about 24 hours, resulting mainly from arteriosclerosis, emboli, or hypertensive episodes. (12 Dec 1998) |
| transient | 1. Short-lived; passing; not permanent; said of a disease or an attack. 2. A short-lived cardiac sound having little duration (less than 0.12 second) as distinct from a murmur; e.g., first, second, third, and fourth heart sounds, clicks, and opening snaps. Origin: L. Transeo, pres. P. Transiens, to cross over (05 Mar 2000) |
| transient acantholytic dermatosis | A pruritic papular eruption, with histologic suprabasal acantholysis, of the chest, with scattered lesions of the back and lateral aspects of the extremities, lasting from a few weeks to several months; seen predominantly in males over 40. Synonym: Grover's disease. (05 Mar 2000) |
| transient agammaglobulinaemia | A type of primary immunodeficiency that occurs in infants of both sexes, usually before the sixth month of life, probably resulting from immaturity of lymphoid tissue. Synonym: transient agammaglobulinaemia. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|