| 영문 | eosinophilia | 한글 | 호산구증가증 |
|---|---|---|---|
| 설명 | 말초혈액속의 호산구 정상치는 1mL 당 약 0.05×100에서 0.4×100인데, 이 범위를 넘어서 호산구가 증가한 상태. 호산구 수는 출생 직후부터 늘어나기 시작하여 6~8세 경에 최고치에 이르게 되는데, 소아는 평균 240/mm3개이고 성인은 평균 150/mm3개이다. 성인의 경우 말초혈액내 호산구 수가 500/mm3개 이상일 때 호산구가 늘어났다고 한다. 원인질환으로는 알레르기질환, 기생충질환, 혈액질환, 호흡기질환 등이 있으며, 피부병, 감염병, 악성종양 등이 원인병으로 나타난다. |
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| FHH | Familial Hypocalciuric Hypercalcemia = Familial Benign Hypercalcemia |
|---|---|
| FAD | familial Alzheimer dementia; familial autonomic dysfunction; fetal activity-acceleration determinati... |
| FAP | familial adenomatous polyposis; familial amyloid polyneuropathy; fatty acid polyunsaturated; fatty a... |
| ALHE | angiolymphoid hyperplasia with eosinophilia |
| BEAP | bronchiectasis, eosinophilia, asthma, pneumonia |
| ALHE | Angiolymphoid hyperplasia with eosinophilia |
|---|---|
| EMS | Eosinophilia Myalgia Syndrome |
| TPE | Tropical Pulmonary Eosinophilia |
| TATE | Tumor-associated tissue eosinophilia |
| BFNC | Benign Familial Neonatal Convulsions |
| acute pulmonary eosinophilia | <chest medicine> A self-limiting inflammation in the lungs where there is associated infiltration of eosinophils into lung tissue. Chest X-ray reveals pulmonary infiltrates and full blood count shows increased numbers of eosinophils. The cause is unknown and the disease often resolves without treatment. Some forms may be treated with oral corticosteroids. Complications include restrictive cardiomyopathy due to fibrosis of the lining of the heart. (27 Sep 1997) |
|---|---|
| angiolymphoid hyperplasia with eosinophilia | Solitary or multiple benign cutaneous nodules comprised of immature and mature vascular structures intermingled with endothelial cells and a varied infiltrate of eosinophils, histiocytes, lymphocytes, and mast cells. (12 Dec 1998) |
| pulmonary eosinophilia | A disease characterised by pulmonary infiltrations of eosinophils and blood eosinophilia. (12 Dec 1998) |
| simple pulmonary eosinophilia | Pulmonary infiltrates seen as transient migratory shadows on the chest X-ray, accompanied by blood eosinophilia; often symptomless, but there may be cough, fever, and breathlessness; most cases are due to worm infestation, especially by Ascaris lumbricoides; a few cases follow administration of drugs. Synonym: Loffler's syndrome. (05 Mar 2000) |
| eosinophilia | <haematology> The formation and accumulation of an abnormally large number of eosinophils in the blood. Origin: Gr. Philein = to love (18 Nov 1997) |
| eosinophilia-myalgia syndrome | <syndrome> A complex systemic syndrome with inflammatory and autoimmune components that affect the skin, fascia, muscle, nerve, blood vessels, lung, and heart. The varied symptoms include severe muscle pain and abnormally high numbers of eosinophils. This disease has presented itself only in people taking the amino acid l-tryptophan and it is believed that a specific impurity (probably stemming from a genetically engineered bacterial strain) in lots of l-tryptophan made by a single manufacturer may be the cause of the syndrome. (12 Dec 1998) |
| tropical eosinophilia | <chest medicine, infectious disease> Eosinophilia associated with cough and asthma, caused by occult filarial infection without evidence of microfilaraemia, occurring most frequently in India and Southeast Asia. (05 Mar 2000) |
| benign familial chorea | A rare, nonprogressive movement disorder characterised by chorea and athetosis appearing in early childhood, most commonly manifested as gait ataxia and upper limb coordination. Intellect is unaffected. Probably autosomal-dominance inheritance with incomplete penetrance. (05 Mar 2000) |
| benign familial chronic pemphigus | Recurrent eruption of vesicles and bullae that become scaling and crusted lesions with vesicular borders, predominantly of the neck, groin, and axillary regions; autosomal dominant inheritance, presenting in late adolescence or early adult life. Synonym: Hailey-Hailey disease. (05 Mar 2000) |
| benign familial icterus | Mild jaundice due to increased amounts of unconjugated bilirubin in the plasma without evidence of liver damage, biliary obstruction, or haemolysis; thought to be due to an inborn error of metabolism in which the excretion of bilirubin by the liver is defective, ascribed to decreased conjugation of bilirubin as a glucuronide or impaired uptake of hepatic bilirubin. Synonym: benign familial icterus, constitutional hepatic dysfunction, Gilbert's disease, Gilbert's syndrome, Hebra's disease. (05 Mar 2000) |
| cancer, breast, familial | A number of factors have been identified that increase the risk of breast cancer. One of the strongest of these risk factors is the history of breast cancer in a relative. About 15-20% of women with breast cancer have such a family history of the disease, clearly reflecting the participation of inherited (genetic) components in the development of some breast cancers. Dominant breast cancer suceptibility genes, including BRCA1 and BRCA2, appear responsible for about 5% of all breast cancer. (12 Dec 1998) |
| paralysis, familial periodic | An autosomal dominant trait marked by recurring attacks of rapidly progressive flaccid paralysis. There are three types: I, associated with a fall in serum potassium levels (hypokalaemic periodic paralysis); II, associated with a rise therein (hyperkalaemic periodic paralysis, called also adynamia episodica hereditaria); and III, with normal levels (normokalaemic periodic paralysis). (12 Dec 1998) |
| pemphigus, benign familial | Rare hereditary disease characterised by recurrent eruptions of vesicles and bullae mainly on the neck, axillae, and groin. It exhibits autosomal dominant inheritance and is unrelated to pemphigus vulgaris though it closely resembles that disease. (12 Dec 1998) |
| chronic familial icterus | <haematology> A hereditary disorder that leads to a chronic haemolytic anaemia due to an abnormality in the red blood cell membrane. This disorder is caused by a defective gene. Red cells are resistant to stress and rupture easily. Infants may appear jaundiced and pale. Fatigue, weakness and shortness of breath are other symptoms that may be seen in older patients. The spleen may also be enlarged. Treatment includes splenectomy (removal of the spleen). After this is accomplished the life-span of the red blood cells returns to normal. (27 Sep 1997) |
| chronic familial jaundice | <haematology> A hereditary disorder that leads to a chronic haemolytic anaemia due to an abnormality in the red blood cell membrane. This disorder is caused by a defective gene. Red cells are resistant to stress and rupture easily. Infants may appear jaundiced and pale. Fatigue, weakness and shortness of breath are other symptoms that may be seen in older patients. The spleen may also be enlarged. Treatment includes splenectomy (removal of the spleen). After this is accomplished the life-span of the red blood cells returns to normal. (27 Sep 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|