| 영문 | Paget's disease | 한글 | 파제트병 |
|---|---|---|---|
| 설명 | 1. 뼈파제트병. 변형성 뼈염. 뼈흡수 후 뼈형성이 반복적으로 과도하게 일어나는 것으로, 새롭게 형성된 뼈는 무질서하고 구조적으로 견고하지 못하다. 뼈흡수의 증가가 반복되고 이어서 과잉보수를 꾀하여 약하고 변형된 뼈의 부피가 증가되는 것을 특징으로 하는 뼈병이다. 궁둥뼈의 만곡, 편평뼈의 변형을 일으키고, 동통 및 병적 골절을 수반한다. 2. 유방파제트병. 젖꽃판 및 젖꼭지의 염증성 암성 질병으로서 보통은 젖샘 및 유방 깊은 곳의 암을 동반한다. 보통 중년부인에게 발생한다. |
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| 영문 | endemic disease | 한글 | 풍토병 |
|---|---|---|---|
| 설명 | 인간사회에 항상 존재하지만 특수한 기후나 토질로 인하여 특정지역에만 존재하는 사망률이 낮고, 임상적으로도 드물게 볼 수 있는 병. 특히 그 토지의 풍토-기후-생물-토양 등의 자연환경과 그 지방 주민의 풍속-습관-인습 등이 복잡하게 얽혀서 생긴 특수한 병을 가리킨다. 일반적으로 그 지방 주민의 사망률은 그다지 높지 않지만 근절되기 어려운 것이 특징이다. 지방병이라는 말은 어느 지방에 한정하여 볼 수 있는 병이라는 점에서는 같지만, 풍토환경과 밀접한 관계가 있다는 데서 보면 풍토병이라는 용어가 적절하다. 국내적으로는 쯔쯔가무시병, 야생토끼병, 렙토스피라증 등이 알려져 있고, 세계적으로는 말라리아, 황열, 페트스, 일본주혈흡충증 등이 알려져 있다. |
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| 영문 | Hodgkin's disease | 한글 | 호지킨병 |
|---|---|---|---|
| 설명 | 악성림프종의 한 형태이다. 호지킨병은 방사선 치료에 대단히 예민해서 충분한 양의 방사선으로 완전한 근치적 치료가 가능하다. |
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| LCP Disease | Legg-Calve-Perthes Disease ? Stages of LCP Disease(= Juvenile Idiopathic AVN) &nb... |
|---|---|
| AID | acquired immunodeficiency disease; acute infectious disease; acute ionization detector; Agency for I... |
| BD | barbital-dependent; barbiturate dependence; base deficit; base of prism down; basophilic degeneratio... |
| CAD | cadaver, cadaveric; cold agglutinin disease; compressed air disease; computer-assisted design; compu... |
| CSD | carotid sinus denervation; cat scratch disease; combined system disease; conditionally streptomycin ... |
| Batten-Mayou disease | Cerebral sphingolipidosis, late infantile and juvenile types. (05 Mar 2000) |
|---|---|
| Bayle's disease | <neurology> Slight or incomplete paralysis. Origin: Gr. = relaxation (18 Nov 1997) |
| Bazin's disease | A type of panniculitis characterised histologically by the presence of granulomas, vasculitis, and necrosis. It is traditionally considered to be the tuberculous counterpart of nodular vasculitis, but is now known to occur without tuberculous precedent. It is seen most commonly in adolescent and menopausal women, is initiated or exacerbated by cold weather, and typically presents as one or more recurrent erythrocyanotic nodules or plaques on the calves. The nodules may progress to form indurations, ulcerations, and scars. (12 Dec 1998) |
| Bechterew's disease | Arthritis and osteitis deformans involving the spinal column; marked by nodular deposits at the edges of the intervertebral disks with ossification of the ligaments and bony ankylosis of the intervertebral articulations, it results in a rounded kyphosis with rigidity. Synonym: Bechterew's disease, poker back, Strumpell's disease. (05 Mar 2000) |
| Becker's disease | An obscure South African cardiomyopathy leading to rapidly fatal congestive heart failure and idiopathic mural endomyocardial disease. (05 Mar 2000) |
| Begbie's disease | Localised chorea. (05 Mar 2000) |
| Beguez Cesar disease | Chediak-Higashi syndrome |
| Behcet's disease | <syndrome> A multisystem, chronic recurrent disease characterised by ulceration in the mouth and genitalia, iritis, uveitis, arthritis and thrombophlebitis. Often treated with immunosuppressive therapy (corticosteroids, chlorambucil). (27 Sep 1997) |
| Behr's disease | <syndrome> Adult or presenile form of heredomacular degeneration. Synonym: Behr's disease. (05 Mar 2000) |
| Berger's disease | <disease, nephrology> This is a form of glomerulonephritis that results from the deposition of circulating IgA antibody in the kidney tissues. Inflammation of the glomerulus (glomerulonephritis) is the result and may present as acute glomerulonephritis, chronic glomerulonephritis or rapidly progressive glomerulonephritis. Berger's disease is usually detected in an individual with one or two bouts of haematuria (usually begins during or soon after a respiratory infection) and no other symptoms of renal disease. Only rarely, will Berger's disease permanently affect kidney function and progress to chronic renal failure. This renal disorder more commonly affects males in the 16-40 age group. (11 Jan 1998) |
| Bernard-Soulier disease | An autosomal recessive disorder of absent or decreased platelet membrane glycoproteins Ib, IX, and V (the receptor for factor VIII R. This deficiency can lead to a failure to bind von Willebrand factor, causing moderate bleeding. (05 Mar 2000) |
| Bernhardt's disease | <symptom> A tingling, formication, itching, and other forms of paresthesia in the outer side of the lower part of the thigh in the area of distribution of the lateral femoral cutaneous nerve; there may be pain, but the skin is usually hypesthetic to the touch. Synonym: Bernhardt's disease, Bernhardt-Roth syndrome, Roth's disease, Roth-Bernhardt disease. (21 Sep 2000) |
| Besnier-Boeck-Schaumann disease | <disease> Disease of unknown aetiology in which there are chronic inflammatory granulomatous lesions in lymph nodes and other organs. (18 Nov 1997) |
| Best's disease | <disease> Autosomal dominant retinal degeneration in the first several years of life. Inheritance: autosomal dominant. (27 Sep 1997) |
| Bielschowsky's disease | Early childhood type of lipofuscinosis. (05 Mar 2000) |