| 영문 | Crohn's disease | 한글 | 크론병 |
|---|---|---|---|
| 설명 | 만성적이고 재발을 잘하는 창자의 염증을 특징으로 하는 병. 장의 벽은 안쪽에서부터 점막, 점막하조직, 근육층, 장막의 4개의 층으로 이루어져 있는데, 크론병은 이 모든 층의 염증을 동반한다. 장의 모든 부분에서 생길 수가 있지만 주로 막창자와 연결되는 큰창자의 말단부에 가장 많이 생긴다. 창자의 전층의 염증으로 인해서 장의 폐쇄나 괴양을 만들며 종종 천공된다. |
||
| 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. |
||
| 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. |
||
| 영문 | infectious disease | 한글 | 감염병 |
|---|---|---|---|
| 설명 | 바이러스로부터 기생충 크기까지의 생물을 원인으로 하는 병. 원인은 접촉전염성이며, 병원에서 감염되는 경우도 있다. 감염을 원인균에 따라 분류하면 바이러스, 세균, 클라미디아, 리켓차, 미코박테리움, 곰팡이, 원충, 윤충, 외부기생충 감염으로 나눌 수 있다. |
||
| 영문 | hypertensive heart disease | 한글 | 고혈압심장병 |
|---|---|---|---|
| 설명 | 고혈압에 의해서 생기는 심장병. 고혈압심장병이라는 진단을 붙이기 위해서는 최소한 다음과 같은 조건이 부합되어야 하는데, 첫째 심장혈관계에 심장병을 유발할 수 있을 만한 다른 병변이 없이 좌심실 비대가 있어야 하며, 둘째 고혈압을 앓았다는 병력이 있어야 한다. 주로 고혈압에 의한 심장병은 초기에는 좌심실이 비후라는 것으로 특징되어진다. 즉 혈압이 높으므로 혈액을 순환시키기 위해서는 그만큼 심장의 혈액을 보내는 힘이 좋아야 한다. 그 힘을 얻기위해서는 심근의 비후가 필요로 하여 좌심실 근육의 비후가 생긴다. 그리고 고혈압이 지속이 될 경우에는 결국 심장이 제 구실을 하지 못하고 펌프로서의 기능을 잃어버리게 되어 심장기능상실에 빠지게 된다. |
||
| CD | cadaver donor; canine distemper; canine dose; carbohydrate dehydratase; carbon dioxide; cardiac dise... |
|---|---|
| JRA | Juvenile Rheumatoid Arthritis; 연소기 류마토이드 관절염 = Juvenile Chronic Arthritis; 연소기 만성 관절... |
| ABCDES | abnormal alignment, bones-periarticular osteoporosis, cartilage-joint space loss, deformities, margi... |
| HD | Haab-Dimmer [syndrome]; Hajna-Damon [broth]; Hansen disease; hearing distance; heart disease; helix ... |
| MD | Doctor of Medicine [Lat. Medicinae Doctor]; magnesium deficiency; main duct; maintenance dose; major... |
| CD | Crohn Disease |
|---|---|
| CDAI | Crohn Disease Activity Index |
| JA | Juvenile Arthritis |
| JCA | Juvenile Chronic Arthritis |
| JIA | Juvenile Idiopathic Arthritis |
acute arthritis
| 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) |
|---|---|
| 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) |
| systemic-onset juvenile chronic arthritis | See: Systemic-onset juvenile rheumatoid arthritis (still's disease). (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 chronic arthritis | juvenile arthritis |
| juvenile chronic arthritis, systemic-onset | See: Juvenile rheumatoid arthritis, systemic-onset (still's disease). (12 Dec 1998) |
| 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) |
| crohn disease | <radiology> CT: double halo (50%): edematous mucosa/thickened soft tissue, creeping fat (40%): mesenteric infiltration, ultrasound: thickened bowel wall (65%): about 8mm, inflammatory mass (14%), abscess (4%), distended fluid filled loops (12%), Complications: fistula (33%), intramural sinus tracts, abscess, perforations (rare), toxic megacolon, SBO (15%), hydronephrosis (usually right sided), adenocarcinoma in ileum/colon, Differential diagnosis: Yersinia: in TI, resolution in 3-4 months, TB (more severe involvement of caecum), segmental infarction (acute onset, elderly patient), radiation ileitis, lymphoma, carcinoid, eosinophilic gastoenteritis, potassium stricture see: sites, phases, extraintestinal manifestations Cf: ulcerative colitis More info: Crohn disease (12 Dec 1998) |
| crohn disease: extraintestinal manifestations | <radiology> Fatty liver, gallstones (28-34%), risk 3-5X higher than expected, secondary to malabsorption of bile salts in terminal ileum, correlation with length of diseased ileum and duration of disease, sclerosing cholangitis, bile duct carcinoma, amyloidosis, urolithiasis: oxalate/uric acid stones, migratory arthritis (5-20%), sacroilitis, ankylosing spondylitis, erythema nodosum, uveitis see: Crohn disease (12 Dec 1998) |
| crohn disease: phases | <radiology> Nonstenotic phase: blunting, flattening, distortion, straightening, and thickening of mucosal folds (early event from obstructive lymphadema), aphthous ulcers: nodules with shallow central ulcerations, cobblestoning: serpiginous ulcers separated by areas of oedema, pseudopolyps: hyperplastic mucosa between denuded mucosa, postinflammatory polyps, skip lesions (90%), pseudodiverticula: bulging area of normal wall opposite affected scarred wall, mostly on the antimesenteric side, separation and displacement of small bowel loops (from increase in mesenteric fat, enlarged nodes, or perforation with abscess formation), stenotic phase: string sign: strictures (most in TI) in rigid loops, normal proximal loops may be dilated with stasis ulcers and fecoliths see: Crohn disease (12 Dec 1998) |
| crohn disease: sites | <radiology> Oesophagus: rare, stomach (2-20%): granulomatous gastritis, pseudo-post Bilroth-I appearance, ramshorn sign, antral-duodenal fistula, duodenum (4-10%): almost always associated with gastric involvement, bulb and proximal half of duodenum, small bowel (80%): regional enteritis, terminal ileum (alone/in combination): 95%, jejunum/ileum: 15%, commonly associated with medial caecal defect, colon (22-55%): granulomatous colitis, particularly on the right side, transverse stripe sign: contrast within coarse mucosal folds, rectum (35-50%) see: Crohn disease (12 Dec 1998) |
| crohn disease vs ulcerative colitis | <radiology> Crohn disease ulcerative colitis location right side left side ulcers deep shallow contraction no yes ileocaecal valve thickened gaping fistulae yes no eccentricity yes no rate of carcinoma slight increase marked increase megacolon unusual yes (12 Dec 1998) |
| Crohn's disease | <disease, gastroenterology> An inflammatory disease of the gastrointestinal tract that seems to have both genetic and environmental causes, not well understood. The peak incidence of onset of this disease is between 15 and 25 years of age. Crohn's also occurs in later years between the ages of 55 and 60. Common symptoms include recurrent abdominal pains, fever, nausea, vomiting, weight loss and diarrhoea which is occasionally bloody. Complications include gastrointestinal bleeding, fistulas and anal fissures. Treatment includes anti-inflammatory drugs and corticosteroids. Surgery is successful in a select few. (27 Sep 1997) |
| disease, crohn's | A chronic inflammatory disease of the intestine. Named after Burrill Crohn who described the disease in 1932. It usually affects persons in their teens or early twenties. It tends to be a chronic, recurrent condition withperiods of remission and exacerbation. In the early stages, there are small scattered shallow crater-like areas (erosions) called apthous ulcers in the inner surface of the bowel. With time, deeper and larger ulcers develop, causing scarring and stiffness of the bowel. The bowel becomes increasingly narrowed, leading to obstruction. Deep ulcers can puncture holes in the bowel wall, leading to infection in the abdominal cavity (peritonitis)and in adjacent organs. When only the large intestine (colon) is involved, the condition is called Crohn's colitis. When only the small intestine is involved, the condition is called Crohn's enteritis. When only the end of the small intestine (the terminal ileum) is involved, it is termed terminal ileitis.When both the small intestine and the large intestine are involved, the condition is called Crohn's enterocolitis (or ileocolitis). Abdominal pain, diarrhoea, vomiting, fever, and weight loss can be symptoms. Crohn's disease can be associated with reddish tender skin nodules, and inflammation of the joints, spine, eyes, and liver. Diagnosis is by barium enema, barium X-ray of the small bowel, and colonoscopy. Treatment includes medications for inflammation, immune suppression, antibiotics, orsurgery. (The disease is also called granulomatous enteritis or regionalenteritis). (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|