| 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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| 영문 | systemic lupus erythematosus | 한글 | 전신홍반루푸스 |
|---|---|---|---|
| 설명 | 전신 자가면역병의 대표적 병이다. 여성에게 압도적으로 많고, 10~39세까지가 70%를 차지한다. 원인은 잘 모르나 자가면역 조절기능에 장애가 있는 것으로 생각된다. 유전요인, 호르몬의 영향, 환경요소가 종합적으로 보조 T세포와 B세포를 활성화시켜서 여러 가지 자가항체들, 즉 천연 DNA, 이중가닥 DNA, 외가닥 DNA, RNA, 핵단백질 등과 같은 핵 항원에 대한 항체, 비핵항원에 대한 여러 가지 항체가 쏟아져 나온다. 이 중 이중가닥 DNA를 포함한 순환면역복합체가 콩팥에 침착하여 손상을 일으키는데 관여한다. DNA와 여러 가지 세포성분에 대한 자가면역질환으로 전콩팥기를 침범하여 염증을 일으킨다. 여러 자가항원에 대한 면역반응에 의한 항체의존성 면역반응과 면역복합체 반응으로 토리콩팥염, 혈관염, 관절염 및 빈혈을 동반한다. |
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| 영문 | systemic circulation | 한글 | 체순환 |
|---|---|---|---|
| 설명 | 왼심실에서 신체를 돌아 오른심방까지의 순환을 의미하며, 왼심실 → 대동맥 → 동맥 → 모세혈관 → 정맥 → 대정맥 → 오른심방의 회로를 순환한다. |
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| PSS | painful shoulder syndrome; physiologic saline solution; porcine stress syndrome; primary Sjogren syn... |
|---|---|
| SMCD | senile macular choroidal degeneration; systemic mast cell disease; systemic meningococcal disease |
| SSc | systemic scleroderma; systemic sclerosis |
| AV | Adriamycin and vincristine; air velocity; allergic vasculitis; anteroventral; anteversion; anticipat... |
| CNV | choroidal neovascularization; contingent negative variation; cutaneous necrotizing vasculitis |
| SV | systemic vasculitis |
|---|---|
| HUVS | Hypocomplementemic urticarial vasculitis syndrome |
| LCV | Leukocytoclastic vasculitis |
| RV | rheumatoid vasculitis |
| MAP | Mean systemic arterial pressure |
| 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) |
| rheumatoid arthritis, systemic-onset juvenile | 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 appear and may persist after the systemic symptoms are gone. (12 Dec 1998) |
| portal-systemic anastomoses | Naturally-occurring venous communications between tributaries of the portal venous system and tributaries of the systemic venous system. The major portal-systemic anastomoses include: 1) oesophageal branches of left gastric vein with oesophageal veins, 2) superior rectal vein with middle and inferior rectal veins, 3) paraumbilical veins with subcutaneous veins of anterior abdominal wall, 4) retroperitoneal veins with venous branches of veins of the colon and bare area of the liver, and 5) a patent ductus venosus connecting left branch of portal vein to inferior vena cava (rare). These anastomoses are important clinically, providing collateral circulation during portal obstruction or hypertension, at which time they may become varicose. See: caput medusae, oesophageal varices, haemorrhoids. Surgically-created communications between the portal vein and the inferior vena cava or their tributaries, to relieve portal hypertension. Synonym: portacaval anastomoses. (05 Mar 2000) |
| portal-systemic encephalopathy | An encephalopathy associated with cirrhosis of the liver, attributed to the passage of toxic nitrogenous substances from the portal to the systemic circulation; cerebral manifestations may include coma. Synonym: hepatic encephalopathy. (05 Mar 2000) |
| scleroderma, systemic | A chronic, progressive dermatosis characterised by boardlike hardening and immobility of the affected skin, with visceral involvement, especially of lungs, oesophagus, kidneys and heart. It may be accompanied by calcinosis, raynaud's phenomenon, and telangiectasis (crest syndrome). It includes acrosclerosis and sclerodactyly. (12 Dec 1998) |
| systemic | <anatomy> Pertaining to or affecting the body as a whole. (18 Nov 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|