| 영문 | rheumatoid arthritis | 한글 | 류마티스관절염 |
|---|---|---|---|
| 설명 | 만성의 관절병으로 보통 여러 관절을 침범하며, 윤활막(관절을 둘러싸고 있으며, 관절의 움직임을 마찰없이 원활하게 수행되도록 함), 관절구조의 염증성 변화와 뼈의 위축과 소모가 두드러진다. 말기에는 변형과 강직이 일어나며 원인은 불명이나 자가면역성 또는 바이러스의 감염에 의한 것으로 생각된다. 치료는 계열의 소염진통제가 사용된다. |
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| 영문 | arthritis | 한글 | 관절염 |
|---|---|---|---|
| 설명 | 관절에 일어난 염증. 원인에 따라 화농성-결핵성-매독성 등 감염성과 류마티스에 의한 것, 외상으로 인한 것 등으로 나눈다. 임상상으로는 급성과 만성으로 나뉜다. 1. 급성. ① 장액관절염: 보통 외상에 의해 일어나며 원인불명의 것도 있으나 대개 하나의 관절에만 발생한다. ② 장액섬유소관절염: 급성관절 류마티스 때에 일어나며, 관절강내에 혼탁한 삼출액이 고인다. 섬유소의 거짓막이 생겨 염증이 가라앉아도 심한 운동장애를 남긴다. ③ 화농관절염: 관절의 개방창 또는 임질-성홍열-패혈증 같은 전염병에 다발성을 보인다. 생후 1~2개월의 유아는 뼈가 심하게 상하여 치료할 수 없는 탈구를 일으킨다. 성인에서는 뼈막골수염에 걸려 화농부가 터져 고름이 관절로 들어가는 것이 많으며, 이를 2차화농관절염이라고 한다. 2. 만성. ① 특수염증: 결핵성-매독성 혹은 중년 이후의 남자에 많은 요산의 대사 장애로 인한 통풍성 관절염이 있다. ② 다발관절염: 만성관절 류마티스에 의한 것이 많으며 급성장액관절염에서 이행한 것과 결핵-매독-임질의 경과 중에 볼 수 있는 다발성 및 패혈증의 하나도 있고, 여기에는 스틸병이라는 관절염도 포함된다. ③ 변형골관절염: 뼈나 관절의 노화 또는 외상이 원인이다. ④ 혈우병괄절염: 혈우병을 앓을 때 관절 내의 출혈에 의한 것이다. |
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| 영문 | rheumatoid factor | 한글 | 류마티스 인자 |
|---|---|---|---|
| 설명 | IgG의 Fc부위에 있는 항원결정인자에 대한 항체로서 전형적인 또는 확실한 류마티스관절염(rheumatoid arthritis) 환자의 80%에서 발견된다. 류마티스 인자는 IgM, IgG, IgA중 하나가 될 수 있으나 주로 IgM이다. 소아류마티스관절염(juvenile rheumatoid arthritis: 소아기에 발생하는 류마티스관절염)을 비롯한, 다른 결합조직병이나 감염병에도 나타날 수 있다 |
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| ABCDES | abnormal alignment, bones-periarticular osteoporosis, cartilage-joint space loss, deformities, margi... |
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| CHRONIC | chronic disease, rheumatoid arthritis, neoplasms, infections, cryoglobulinemia [conditions in which ... |
| JRA | Juvenile Rheumatoid Arthritis; 연소기 류마토이드 관절염 = Juvenile Chronic Arthritis; 연소기 만성 관절... |
| RA | 1) Refractory Anemia 2) Rheumatoid Arthritis ? Arthritis 3... |
| RA | radioactive; ragocyte; ragweed antigen; rapidly adapting [receptors]; reactive arthritis; reciprocal... |
| J.R.A. | Juvenile Rheumatoid Arthritis |
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| MRA | Malignant rheumatoid arthritis |
| RANA | rheumatoid arthritis nuclear antigen |
| IgA RF | IgA rheumatoid factor |
| RF | IgA-rheumatoid factor |
self-care (자가 치료
acute arthritis
| rheumatoid arthritis | <rheumatology> Chronic inflammatory disease in which there is destruction of joints. Considered by some to be an autoimmune disorder in which immune complexes are formed in joints and excite an inflammatory response (complex mediated hypersensitivity). Cell-mediated (type IV) hypersensitivity also occurs and macrophages accumulate. This in turn leads to the destruction of the synovial lining (see pannus). (18 Nov 1997) |
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| 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) |
| rheumatoid arthritis: joint manifestations | <radiology> Early signs: fusiform periarticular soft tissue swelling (result of effusion), regional osteoporosis (disuse and local hyperaemia), widened joint space, marginal and central bone erosion (base of 4th proximal phalanx most common), change in ulnar styloid and distal radioulnar joint, atlantoaxial dislocation, giant synovial cysts late signs: flexion/extension contractures with ulnar subluxation/dislocation, destruction/fusion of joints, elevation of humeral heads (tear/atrophy of rotator cuff), resorption of distal clavicle, erosion of superior margins of posterior portions of 3-5th ribs, destruction/narrowing of disc spaces, destruction of zygapophyseal joints without osteophyte formation, resorption of spinous process, protrusio acetabuli (from osteoporosis) (12 Dec 1998) |
| arthritis, juvenile rheumatoid | Rheumatoid arthritis of children occurring in three major subtypes defined by the symptoms present during the first six months following onset: systemic-onset (still's disease, juvenile-onset) polyarticular-onset, and pauciarticular-onset. Adult-onset cases of still's disease (still's disease, adult-onset) are also known. Only one subtype of juvenile rheumatoid arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent. (12 Dec 1998) |
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| arthritis, rheumatoid | Autoimmune disease that is characterised by chronic inflammation of the joints and can cause inflammation of tissues in other areas of the body (such as the lungs, heart, and eyes). (12 Dec 1998) |
| systemic-onset juvenile rheumatoid arthritis | <rheumatology> A form of joint disease, arthritis, that presents with systemic upset. Clinical signs: 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 itself may not be immediately apparent but once apparent, it may persist after the systemic symptoms have resolved. Synonym: Still's disease. (03 Jul 1999) |
| juvenile rheumatoid arthritis | <pathology> Juvenile rheumatoid arthritis (JRA) is a form of rheumatoid arthritis in children that generally occurs prior to age 16. In contrast with the adult type, a fever is more pronounced. Cardiac involvement with pericarditis is more common. The arthritis favors one or more large joints and can interfere with normal bone growth. A positive rheumatoid factor is seen more uncommonly in this form of arthritis. Treatment is similar to the adult form of the disease. Up to 75% recover with treatment. Less than 10% are severely disabled by JRA. (27 Sep 1997) |
| juvenile rheumatoid arthritis, systemic-onset | 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 always surface and it may persists long after the systemic symptoms are gone. (12 Dec 1998) |
| anarthritic rheumatoid disease | Rheumatoid disease without arthritis. (05 Mar 2000) |
| rheumatoid | <pathology> Resembling rheumatism. Origin: Gr. Rheuma = flux, eidos = form (18 Nov 1997) |
| rheumatoid arteritis | Coronary arteritis associated with rheumatoid arthritis; aortitis with aortic valve incompetence accompanying ankylosing spondylitis may be related. (05 Mar 2000) |
| rheumatoid disease | Rheumatoid arthritis, referring particularly to nonarticular lesions such as subcutaneous nodules. (05 Mar 2000) |
| rheumatoid factor | Complex of IgG and anti-igG formed in joints in rheumatoid arthritis. Serum rheumatoid factors are more usually formed from IgM antibodies directed against IgG. (18 Nov 1997) |
| rheumatoid factors | Antibodies in the serum of individuals with rheumatoid arthritis that react with antigenic determinants or immunoglobulins that enhance agglutination of suspended particles coated with pooled human gamma-globulin. Rheumatoid factors also occur in other autoimmune and certain infectious diseases. (05 Mar 2000) |
| rheumatoid lung disease | <radiology> Pleural effusion, most common finding, seen mostly in males (although RA more common in females), diffuse interstitial fibrosis, necrobiotic nodules, Caplan syndrome, nodules and pneumoeritis and hypertension (12 Dec 1998) |
| rheumatoid nodule | Subcutaneous nodules seen in 20-30% of rheumatoid arthritis patients. They may arise anywhere on the body, but are most frequently found over the bony prominences. The nodules are characterised histologically by dense areas of fibrinoid necrosis with basophilic streaks and granules, surrounded by a palisade of cells, mainly fibroblasts and histiocytes. (12 Dec 1998) |
| rheumatoid nodules | rheumatoid nodules are firm lumps in the skin of patients with rheumatoid arthritis that usually occur in pressure points of the body, most commonly the elbows (12 Dec 1998) |
| rheumatoid spondylitis | <rheumatology> A polyarthritis involving the spine, which is characterised by progressive, painful stiffening of the joints and ligaments. It almost exclusively affects young men. Interestingly the disease seems to be associated with HLA B27, those with this histocompatability antigen are 300 times more likely to get the disease, 90% of sufferers have HLA B27 (18 Nov 1997) |
| rheumatoid arthritis |
a chronic autoimmune disease with inflammation of the joints and marked deformities; something (possibly a virus) triggers an attack on the synovium by the immune system, which releases cytokines that stimulate an inflammatory reaction that can lead to the destruction of all components of the joint
출처: wordnet.princeton.edu/perl/webwn
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| rheumatoid arthritis |
a condition in which joints in the body become inflamed, stiff, painful, and sometimes deformed because of the body's own immune system attacking the tissues
출처: www.american-depot.com/services/resources_gl_r.asp
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| rheumatoid arthritis |
An immunological disorder that is characterized by symmetrical polyarthritis, often progressing to crippling deformation after years of synovitis. It is associated with systemic immune activation. Acute-phase reactants are present in the peripheral blood, as well as rheumatoid factor (immunoglobulins specific for IgG), which forms immune complexes that are deposited in many tissues.
출처: www.nature.com/nri/journal/v5/n4/glossary/nri1594_...
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| rheumatoid arthritis |
A form of arthritis that affects the lining of the joints. White blood cells move from the bloodstream into the synovial membrane, causing the membrane to become inflamed.
출처: www.cnn.com/HEALTH/library/AR/00026.html
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| rheumatoid arthritis |
A chronic disease marked by stiffness and inflammation of the joints, weakness, loss of mobility, and deformity. [Heritage]
출처: www.antiquusmorbus.com/English/EnglishR.htm
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| Rheumatoid Arthritis | a chronic autoimmune disease with inflammation of the joints and marked deformities |
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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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