| 영문 | chronic lymphocytic leukemia | 한글 | 만성림프성 백혈병 |
|---|---|---|---|
| 설명 | 백혈병(leukemia)란 비정상적인 백혈구 세포의 증식에 의해 일어나는 병적인 상태를 말하는데, 흔히 말초혈액에 미분화세포가 나타나며, 정상적인 적혈구세포와 백혈구세포, 혈소판의 급격한 감소를 가져와 정상적인 세포에 의해 행해지는 여러 기능의 감소를 주증상으로 하여 병원에 찾아오게 된다. 따라서 적혈구세포의 감소로 인한 빈혈, 백혈구세포의 감소로 인한 많은 감염증세(흔히 걸리지 않는 세균에 의한 감염, 지나치게 잦은 감기, 폐렴 등), 혈소판세포의 감소로 인한 출혈증상이 나타난다. 또한 피를 생산하는 골수 조직에서는 이런 비정상적인 세포의 증식만을 볼 수 있으며, 정상적인 세포의 증식은 보기 힘들다. 만성림프성 백혈병은 서양에서는 비교적 백혈병 중에서 흔한 형이지만 동양권에서는 아주 드문 백혈병의 형태이다. 대개 60세 이상의 고령층에서 많이 생기고 30세 이하에서는 거의 찾아볼 수가 없다. 혈액검사상에서 림프구의 많은 증가를 볼 수가 있고, 대신에 다른 혈액세포들은 감소를 나타낸다. 백혈병 중 예후가 좋은 편이며 대개 치료는 항암제를 이용한 화학요법을 많이 사용하며, 평균 생존기간은 4~5년이다. |
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| 영문 | vasculitis | 한글 | 혈관염, 맥관염 |
|---|---|---|---|
| 설명 | 혈관에 나타나는 염증. 모세혈관이나 세동맥-세정맥-동맥-정맥에 모두 영향을 미칠 수 있다. 작은 혈관인 경우에는 조직이 파괴되고 국소적으로 출혈이 동반될 수 있다. 피부에서는 작은 붉은빛 또는 자줏빛 점 모양으로 보인다. 더 큰 혈관에 염증이 생기고 혈관이 피부표면에 가까우면 부어오르고 결절을 형성하기도 한다. 또 혈관 내부가 좁아져서 혈류가 줄거나 염증이 생긴 부위에 생긴 혈전에 의하여 내부가 완전히 막힐 수도 있다. 혈류가 줄거나 멈출 경우에는 그 혈관으로부터 혈류 공급을 받는 조직은 썩어 괴사로 진행하기도 한다. 원인은 혈관벽 감염이나 혈관벽의 면역 또는 알레르기성 반응 때문인 것으로 알려져 있는데, 면역반응 또는 알레르기성 반응에 의한 경우가 더 많다. |
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| AV | Adriamycin and vincristine; air velocity; allergic vasculitis; anteroventral; anteversion; anticipat... |
|---|---|
| CNV | choroidal neovascularization; contingent negative variation; cutaneous necrotizing vasculitis |
| CV | cardiac volume; cardiovascular; carotenoid vesicle; cell volume; central venous; cephalic vein; cere... |
| HVUS | hypocomplementemic vasculitis urticaria syndrome |
| LCV | lecithovitellin; leukocytoclastic vasculitis |
| HUVS | Hypocomplementemic urticarial vasculitis syndrome |
|---|---|
| LCV | Leukocytoclastic vasculitis |
| RV | rheumatoid vasculitis |
| SV | systemic vasculitis |
| ALL | Acute Lymphocytic Leukaemia |
| vasculitis | <pathology> Inflammation of a vessel, angiitis. Origin: L. Vasculum = vessel (18 Nov 1997) |
|---|---|
| vasculitis, allergic cutaneous | Vasculitis due to allergic reaction, marked by such cutaneous lesions as papules, macules, vesicles, urticarial wheals, purpura, and small ulcers, and accompanied by itching and usually a slight fever and malaise. (12 Dec 1998) |
| vasculitis, hypersensitivity | Heterogeneous group of disorders characterised by a vasculitic syndrome presumed to be associated with a hypersensitivity reaction following exposure to an antigen such as an infectious agent, a drug, or other foreign or endogenous substance. (12 Dec 1998) |
| cutaneous vasculitis | An acute form of vasculitis which may affect the skin only, but also may involve other organs, with a polymorphonuclear infiltrate in the walls of and surrounding small (dermal) vessels. Nuclear fragments are formed by karyorrhexis of the neutrophils. See: leukocytoclastic vasculitis. Synonym: allergic angiitis, hypersensitivity vasculitis. (05 Mar 2000) |
| hypersensitivity vasculitis | An acute form of vasculitis which may affect the skin only, but also may involve other organs, with a polymorphonuclear infiltrate in the walls of and surrounding small (dermal) vessels. Nuclear fragments are formed by karyorrhexis of the neutrophils. See: leukocytoclastic vasculitis. Synonym: allergic angiitis, hypersensitivity vasculitis. (05 Mar 2000) |
| hypocomplementemic vasculitis | Cutaneous lesions resembling urticaria but lasting more than 24 hours, with biopsy findings of leukocytoclastic vasculitis and variable systemic changes, usually with hypocomplementemia. Synonym: hypocomplementemic vasculitis. (05 Mar 2000) |
| nodular vasculitis | Chronic or recurrent nodular lesions of subcutaneous tissue, especially of the legs of older women, with lobular panniculitis, granulomatous inflammation with multinucleated giant cells, focal necrosis, and obliterative inflammation of the small blood vessels, resembling erythema induratum but without evidence of associated tuberculosis. (05 Mar 2000) |
| urticarial vasculitis | Cutaneous lesions resembling urticaria but lasting more than 24 hours, with biopsy findings of leukocytoclastic vasculitis and variable systemic changes, usually with hypocomplementemia. Synonym: hypocomplementemic vasculitis. (05 Mar 2000) |
| leukocytoclastic vasculitis | Cutaneous acute vasculitis characterised clinically by palpable purpura, especially of the legs, and histologically by exudation of the neutrophils and sometimes fibrin around dermal venules, with nuclear dust and extravasation of red cells; may be limited to the skin or involve other tissues as in Henoch-Schonlein purpura. See: cutaneous vasculitis. Origin: G. Leukos, white, + kytos, cell, + klastos, broken, fr. Klao, to break (05 Mar 2000) |
| livedo vasculitis | Hyaline degeneration of the walls of small dermal blood vessels with occlusion seen with cryoglobulinaemia or in atrophie blanche. (05 Mar 2000) |
| acute lymphocytic leukaemia | <radiology> 95% of cases of leukaemia in children, bone changes in 50-70% of kids (vs. 10% in adults); seen as early as 1 month after onset of symptoms, wrists and knees most commonly affected, bony defects: metaphyseal radiolucent bands! (similar findings in scurvy, JRA, syphilis), osteolytic lesions, periosteal reaction, osteosclerosis (12 Dec 1998) |
| acute non-lymphocytic leukaemia | <haematology> A form of leukaemia which is characterised by the proliferation of immature bone marrow precursor cells in the marrow and immature white blood cells (granulocytes) in the bloodstream. Occurs primarily in adults and in infants under 1 year of age. Complications include abnormal bleeding and susceptibility to infections. Symptoms include fatigue, weight loss, fevers, weakness, pallor, bone pains, bleeding gums, nosebleeds, easy bruising, enlarged lymph nodes and joint pains. Trisomy-8 is the most common cytogenetic abnormality observed, followed by monosomy-7 and monosomy-5. Approximately 8% of cases show trisomy-8, mostly in AML (M1), AM (M4) and acute monocytic leukaemia (M5). Many pre-leukaemic conditions, acute non-lymphocytic leukaemia and secondary leukemia show monosomy-7 or deletion of the long arm of chromosome 7. Treatment includes chemotherapy and/or bone marrow transplant. Acronym: ANLL Incidence: 2.5 cases per 100,000 (all ages). Origin: Gr. Haima = blood (07 Apr 1998) |
| chronic lymphocytic leukaemia | <haematology> A slowly progressing form of leukaemia, characterised by an increased number of the type of white blood cell known as lymphocytes. With about 3, 500 new cases occurring each year in the UK, it is the most common form of leukaemia and occurs predominantly in late middle age onwards. It has variable symptoms and course, but may be diagnosed by chance before the patient develops any clinical symptoms of disease. Acronym: CLL Origin: Gr. Haima = blood (12 Jan 1998) |
| chronic lymphocytic thyroiditis | <endocrinology> Inflammation of the thyroid gland without the formation of pus. Noninfectious nonbacterial thyroid inflammation. (27 Sep 1997) |
| well-differentiated lymphocytic lymphoma | <tumour> Essentially the same disease as chronic lymphocytic leukaemia, except that lymphocytes are not increased in the peripheral blood; lymph nodes are enlarged and other lymphoid tissue or bone marrow is infiltrated by small lymphocytes. Synonym: small lymphocytic lymphoma. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|