| 영문 | amyloidosis | 한글 | 아밀로이드증 |
|---|---|---|---|
| 설명 | 본래 생체에는 없는 당단백질의 일종으로 비정상적으로 아밀로이드단백이 조직이나 장기에 침착되는 병. 발현부위가 전신성인 경우의 아밀로이드증(전신성 아밀로이드증)에는 명백한 원인없이 일어나는 원발성 아밀로드증과 만성화농성 염증이나 결핵 등 소모성 질환에서 찾아볼 수 있는 속발성 아밀로이드증이 있다. 발현부위가 국소성인 경우의 국소성 아밀로이드증으로서는 뇌의 노인반이 그 예이며, 특히 입안에서는 혀나 잇몸에 대한 침착이 현저하고 여러 가지 기능장애를 나타낸다. 조직학적으로는 헤마톡실린 에오진염색에서는 에오진성 무구조인 유리화를 나타내며 콩고레드, 편광상(녹색) 등으로 확인한다. 구조적으로는 아밀로이드 섬유의 집합으로 이루어지는 여러 가지 아밀로이드 침착이 있으며 그것들에 대한 병형이 분류되어 있다. 가족형, 다발성 골수종과 수반하는 형 그리고 가족성 지중해열을 수반하는 형 등이 있다. |
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| AL | absolute latency; acinar lumen; acute leukemia; adaptation level; albumin; alcoholism [and other dru... |
|---|---|
| DAA | decompensated autonomous adenoma; dementia associated with alcoholism; dialysis-associated amyloidos... |
| HCHWA | hereditary cerebral hemorrhage with amyloidosis |
| ECD | Endocardial Cushion Defect |
| ECD | ectrodactyly; electrochemical detector; electron capture detector; endocardial cushion defect; enzym... |
| AL | Amyloidosis |
|---|---|
| DRA | Dialysis related amyloidosis |
| FAF | Familial amyloidosis, Finnish type |
| HCHWA-D | Hereditary cerebral haemorrhage with amyloidosis, Dutch type |
| ENDO | Endocardial |
| partial endocardial cushion defect | <radiology> Incomplete endocardial cushion defect components: ostium primum atrial septal defect, cleft in anterior mitral valve findings: right AV valve is usually normal, with or without mitral insufficiency, communication between LA_RA or LV-RA, occasionally LV-RV Cf: complete endocardial cushion defect (12 Dec 1998) |
|---|---|
| complete endocardial cushion defect | <radiology> Arteriovenous canal components: low atrial septal defect (ostium primum), high VSD, cleft anterior leaflet of mitral valve, cleft septal leaflet of tricuspid valve, one AV valve common to RV and LV with 5-6 leaflets findings: 4-chamber enlargement (R greater than L), mitral insufficiency, associated with congestive heart failure and Eisenmenger syndrome, gooseneck deformity on angiogram (elongation and narrowing of the LV outflow tract during diastole) see also: endocardial cushion defect, partial endocardial cushion defect (12 Dec 1998) |
| endocardial | 1. Pertaining to the endocardium. 2. <medicine> Seated or generated within the heart; as, endocardial murmurs. Source: Websters Dictionary (01 Mar 1998) |
| endocardial cushion defect | <radiology> Persistence of primitive atrioventricular canal and anomalies of AV valves associated with: Down syndrome: in 25% of Trisomy 21 an ECD is present; in 45% of ECD Trisomy 21 is present, asplenia/polysplenia types: complete (AV canal), partial findings: gooseneck deformity on angiogram, increased pulmonary vascularity, enlarged pulmonary artery, enlarged RV, LV, RA; normal LA (secondary to atrial septal defect) (12 Dec 1998) |
| endocardial cushion defects | A spectrum of septal defects associated with persistence of the embryonic atrioventricular canal due to incomplete growth and fusion of the endocardial cushion. (12 Dec 1998) |
| endocardial cushions | A pair of mounds of embryonic connective tissue covered by endothelium, bulging into the embryonic atrioventricular canal; located one dorsally and one ventrally, they grow together and fuse with each other and with the lower edge of the septum primum, dividing the originally single canal into right and left atrioventricular orifices. Synonym: endocardial cushions. (05 Mar 2000) |
| endocardial fibroelastosis | <radiology> Unknown aetiology, diffuse thickening of endocardium, few live more than 2 yrs, limited to left chambers in 80%, causes restrictive cardiomyopathy (12 Dec 1998) |
| endocardial fibrosis | Scarring or collaginosis of the endocardium. Synonym: endocardial sclerosis. (05 Mar 2000) |
| endocardial murmur | A murmur arising, from any cause, within the heart. (05 Mar 2000) |
| endocardial sclerosis | <radiology> Unknown aetiology, diffuse thickening of endocardium, few live more than 2 yrs, limited to left chambers in 80%, causes restrictive cardiomyopathy (12 Dec 1998) |
| amyloidosis | Deposition of amyloid. A common complication of several diseases (leprosy, tuberculosis), often associated with perturbation of the immune system, although there may be immunosuppression or enhancement. (18 Nov 1997) |
| amyloidosis: bone manifestations | <radiology> Joint pain without radiographic findings, osteoporosis, especially in axial skeleton, lytic lesions that destroy cortex and invade soft tissue, wrist, scaphoid and lunate lesions that may extend into the carpal tunnel, inducing the classic complaints of carpal tunnel syndrome amyloid arthropathy Differential diagnosis: pigmented villonodular synovitis, synovial chondromatosis, rheumatoid arthritis, TB (12 Dec 1998) |
| amyloidosis cutis | Localised cutaneous amyloidosis with pruritic brownish-red papules, most commonly on the lower legs, due to amyloid infiltration of the papillary dermis. Synonym: amyloidosis cutis, lichen amyloidosis. Origin: G. Leichen, lichen, a lichen-like eruption + eidos, resemblance (05 Mar 2000) |
| amyloidosis: gastrointestinal manifestations | <radiology> Oesophagus, loss of peristalsis, megaesophagus, stomach, small and rigid (simulate linitis plastica), effaced rugal pattern, diminished/absent peristalsis, may be localised to antrum, amyloidoma: well defined submucosal mass, small bowel, diffuse form (more common), diffuse, uniform thickening of valvulae conniventes, broadened flat undulated mucosal folds (mucosal atrophy), jejunalization of ileum, impaired motility, small bowel dilatation, localised form: multiple small deposits; associated with pseudoobstruction, colon, psudopolyps (12 Dec 1998) |
| amyloidosis of multiple myeloma | Foci of amyloidosis in mesenchymal tissues of some persons with multiple myeloma; no direct relation between amyloid and Bence Jones protein is conclusively known. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|