| 영문 | hyaline membrane disease | 한글 | 유리질막병 |
|---|---|---|---|
| 설명 | 허파 성숙도의 미숙으로 허파꽈리를 팽창시키는 물질(표면활성제)이 부족하여 호흡곤란이 초래되는 병으로서 미숙아에 호발하는데, 출생시 임신기간보다도 허파 성숙 정도가 더 관여된다. 단일 병으로서는 사망률이 가장 높으며(약 30%), 신생아의 대표적인 병이다. 임상적으로는 미숙아, 생후 6~8시간내 호흡곤란증세 출현과 생후 24~48시간의 증상 악화, 생후 2~3일간 인공적으로 산소를 공급하지 않으면 호흡을 계속시킬 수가 없으며 점점더 산소의 공급 의존도가 높아지며, 동맥혈액속의 산소농도가 내려가고 이산화탄소의 농도가 높으며, 흉부 방사선 소견을 참작하여 진단한다. 환아는 숙련된 간호 인력과 첨단 의료 장비가 설치된 신생아 집중 치료실에서 치료하여야 한다. 예후는 증세의 경중에 따라 다르고 사망률은 30~50% 된다. 어떤 아기에 있어서는 치료 후에 눈이나 기관지허파 계통에 장애를 일으키는 산소중독증이 보고되고 있다. |
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| 영문 | fibrocystic disease of breast | 한글 | 유방 섬유낭병 |
|---|---|---|---|
| 설명 | 젖을 생산하는 젖샘내에 완두콩 또는 큰콩 크기의 결절이 발생하는 증세를 특징으로 하는 병. 30~50대의 부인에게 흔히 발생하며, 그 대부분은 양쪽 유방에 동시에 발생한다. 이러한 결절은 두 손가락 사이에 끼워 촉진할 때는 분명하지만, 흉벽을 손바닥으로 누르면 명료하지 않을 정도로 부드러운 것이 많다. 그 발생 원인에는 여러 가지 설이 많은데, 젖샘조직에 대한 만성적인 자극이 주원인이라 생각되고 있으며, 극히 서서히 진행하는 경과를 밟는다. 진단은 촉진, 초음파진단 등으로 하며, 암과 감별이 곤란할 때는 조직의 일부를 채취하여 검사하는 생검이 이용되기도 한다. |
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| 영문 | periodontal disease | 한글 | 치주병 |
|---|---|---|---|
| 설명 | 잇몸과 치아, 그리고 그 주위 뼈의 염증과 퇴행성 변화를 말함. 치료에 있어서 잇몸의 제거가 필수적이다. 잇몸의 제거는 새로운 잇몸의 생성을 조장한다. |
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| 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. |
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| 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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| 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 ... |
| CVD | cardiovascular disease; cerebrovascular disease; collagen vascular disease; color-vision-deviant |
| GBD | gallbladder disease; gender behavior disorder; glass blower's disease; granulomatous bowel disease |
| GD | gastroduodenal; Gaucher disease; general diagnostics; general dispensary; gestational day; Gianotti ... |
| disease, plummer's | Toxic multinodular goiter, a condition in which the thyroid gland contains multiple lumps (nodules) that are overactive and produce excess thyroid hormones. This condition is also known as Parry's disease. (12 Dec 1998) |
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| disease, polycystic kidney | Genetic (inherited) disorders characterised by the development of innumerable cysts in the kidneys filled with fluid that replace much of the mass of the kidneys and reduce kidney function leading to kidney failure. (12 Dec 1998) |
| disease, polycystic ovarian | An hormonal problem that causes women to have a variety of symptoms including irregular or no periods, acne, obesity and excessive hair growth. Women with PCO are at a higher risk for uterine cancer (endometrial cancer), diabetes, high blood pressure, and heart disease. With proper treatment, risks can be minimised. PCO is also known as Stein-Leventhal syndrome. (12 Dec 1998) |
| disease, quincke's | This is angioneurotic oedema (or angioedema), a form of localised swelling of the deeper layers of the skin and fatty tissues beneath the skin. Hereditary angioneurotic oedema (or hereditary angioedema) is a genetic form of angioedema. Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. (12 Dec 1998) |
| disease, refsum's | A genetic disorder of the fatty acid phytanic acid which accumulates and causes a number of progressive problems including polyneuritis (inflammation of numerous nerves), diminishing vision (due to retinitis pigmentosa), and wobbliness (ataxia) caused by damage to the cerebellar portion of the brain (cerebellar ataxia). (12 Dec 1998) |
| disease, ritter | This is the scalded skin syndrome, a potentially serious side effect of infection with the Staph (Staphylococcus) bacteria that produces a specific protein which loosens the cement holding the various layers of the skin together. This allows blister formation and sloughing of the top layer of skin. If it occurs over large body regions it can be deadly (just like a large surface area of the body having been burned). It is necessary to treat scalded skin syndrome with intravenous antibiotics and to protect the skin from allowing dehydration to occur if large areas peel off. The disease occurs predominantly in children under 5 years of age. It is known formally as Staphyloccoccal scalded skin syndrome. (12 Dec 1998) |
| disease, sixth | A viral disease of infants and young children with sudden onset of high fever which lasts several days and then suddenly subsides leaving in its wake a fine red rash. The causative agent is herpes virus type 6 so the disease is known as Sixth Disease. Also known as Exanthem subitum (sudden rash), Pseudorubella, Roseola, Roseola infantilis, and Roseola infantum. (12 Dec 1998) |
| disease, stein-leventhal | See Disease, polycystic ovarian. (12 Dec 1998) |
| disease, still's | Also known as systemic-onset juvenile rheumatoid arthritis and 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 persists after the systemic symptoms are gone. Disease, Still's, adult-onset: Although Still's disease was first described in children, it is known to occur in adults. (12 Dec 1998) |
| disease, subclinical | An illness that stays below the surface of clinical detection. A subclinical disease has no recognizable clinical findings. As distinct from a clinical disease which has clinical signs and symptoms that can be recognised. Many diseases are subclinical before surfacing as clinical diseases. For examples: diabetes, hypothyroidism, rheumatoid arthritis. (12 Dec 1998) |
| disease, tsutsugamushi | Scrub typhus, a mite-borne infectious disease caused by a microorganism, Rickettsia tsutsugamushi, characteristically with fever, headache, a raised (macular) rash, swollen glands (lymphadenopathy) and a dark crusted ulcer (called an eschar or tache noire) at the site of the chigger (mite larva) bite. This disease occurs in the area bounded by Japan, India, and Australia. Known also as mite-borne typhus and tropical typhus. (12 Dec 1998) |
| disease, von recklinghausen's | Hereditary disorder characterised by cafe-au-lait (coffee-with-milk spots on the skin and a tendency to develop nerve tumours) also known as neurofibromatosis. (12 Dec 1998) |
| disease, werner-his | Named for the German physician Heinrich Werner (who did not describe Werner's syndrome) and the Swiss physician Wilhelm His, Jr. (who did describe the bundle of His in the heart), this is a louse-borne disease first recognised in the trenches of World War I (and so called trench fever), again a major problem in the military in World War II, seen endemically in Mexico, N. Africa, E, Europe, and elsewhere. The cause, Rochalimaea quintana, is an unusual rickettsia that multiplies in the gut of the body louse. Transmission to people can occur by rubbing infected louse feces into abraded (scuffed) skin or conjunctiva (whites of the eyes). Onset of symptoms is sudden, with high fever, headache, back and leg pain and a fleeting rash. Recovery takes a month or more. Relapses are common. Also called Wolhynia fever, shin bone fever, quintan fever, five-day fever, Meuse fever, His-Werner disease. (12 Dec 1998) |
| disease-free survival | Period after successful treatment in which there is no appearance of the symptoms or effects of the disease. (12 Dec 1998) |
| diseased | Afflicted with disease. "It is my own diseased imagination that torments me." (W. Irving) Synonym: See Morbid. Source: Websters Dictionary (01 Mar 1998) |
| bartter's disease | Hypertrophy and hyperplasia of the juxtaglomerular cells, producing hypokalaemic alkalosis and hyperaldosteronism, characterised by absence of hypertension in the presence of markedly increased plasma renin concentrations, and by insensitivity to the pressor effects of angiotensin. It usually affects children, is perhaps hereditary, and may be associated with other anomalies, such as mental retardation and short stature. It is also called juxtaglomerular cell aplasia. (12 Dec 1998) |
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| Basedow's disease | <endocrinology> A common cause of hyperthyroidism thought to be caused by an underlying autoimmune mechanism. (27 Sep 1997) |
| basilar interstitial lung disease | <radiology> B bronchiectasis, A asbestosis, D drugs / DIP, L lymphangitic metastasis / LAM, A aspiration, S sarcoidosis, S scleroderma (12 Dec 1998) |
| batten disease | <disease> This congenital disorder strikes between the ages of 5 and 10, causing the afflicted child to suddenly go blind. The child begins to suffer fromseizures and mental deterioration, afflicted individuals typically diebefore the age of 20. The disease is caused by the accumulation of toxicproteins in nerve cells, the root of the disorder is a mutation of a geneon chromosome 16. (09 Oct 1997) |
| 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) |
| disease |
a term of health status; when something is wrong with a bodily function
출처: www.jhsph.edu/publichealthexperts/Glossary.htm
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| disease |
Any abnormality of bodily structure or function, other than those arising directly from injury.
출처: www.canadapharma.org/Patient_Pathways/Glossary_Ter...
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| disease surveillance |
The objective of disease surveillance is to provide early and precise information on key aspects of disease activity such as time, location, virus type, and disease severity. Analysis of this information provides the necessary data to predict disease transmission and guide the implementation of control measures.(31)
출처: www.phdatastandards.info/knowresources/tutorials/g...
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| disease burden |
The total effect of a disease or diseases on an individual as well as society. Knowledge concerning this is important, particularly in attempting to plan prevention programs and in evaluating the success or failure of intervention
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| Disease State Management Program |
ABBR: DSM. A program of health care specific to a designated population (i.e., diabetic patients), offering an organized, systematic pathway to guide clinicians and patients through predetermined steps to measur
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