| 영문 | lung cancer | 한글 | 폐암 |
|---|---|---|---|
| 설명 | 허파에 생기는 악성종양이다. 가장 예후가 나쁜 종양중의 하나로써 조기발견이 어렵고 증세 또한 늦게 나타나서, 그 종양의 종류에 따라 다르나 치료후에도 대개 8%만이 5년 생존이 가능한 악성종양이다. 유발인자로는 대표적으로 담배가 알려져 있으며, 유전적인 요소도 어느 정도 기여하는 것으로 알려져 있다. |
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| 영문 | heart-lung machine | 한글 | 심장-허파 기계 |
|---|---|---|---|
| 설명 | 심장의 수술에 사용되는 기계로서 심장이 수술을 받고 있는 동안 기능을 하지 못하므로 이 기능을 대신 해주는 기계이다. 이것은 대정맥과 대동맥사이에 연결이 되어서 혈액을 강제로 순환시키면서 대정맥에서 온 피에 산소를 공급하여 대동맥으로 돌려 보내는 역할을 한다. 즉 심장과 폐의 역할을 동시에 하는 기계이다. |
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| 영문 | total lung capacity | 한글 | 전폐용량, 온허파용량 |
|---|---|---|---|
| 설명 | 폐활량(가능한 한 깊게 들여 마신 시점부터 천천히 한껏 내쉰 용량)에 잔기량(최대 날숨위치에서 폐내에 남은 용량. 약 1,200mL)을 합한 것이다. 건강한 성인은 6,000~7,000mL. 폐기종, 만성 기관지염 등의 폐색성 장애로 증가하게 되는 한편 허파섬유증, 무기폐, 흉수, 흉곽변형 등의 구속성 장애로 감소한다. |
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| 영문 | ovarian cancer | 한글 | 난소암 |
|---|---|---|---|
| 설명 | 여성의 난소에 발생하는 암. 부인과종양으로서 50세 이상 여성악성종양의 약 18%를 차지한다. 종양은 대개 복부 깊숙히 위치하므로 종양이 많이 진행된 상태에서 발견되는 수가 많으며, 또한 종양의 초기에는 증상이 거의 없는 경우가 많아 더욱 조기발견이 어렵다. 아주 다양한 종류의 암이 발생하며, 예후도 각기 그 종양의 종류에 따라 다르다. 대표적인 암으로 장성낭샘암종(serous cystadenocarcinoma), 점액낭샘암종(mucinous cystadenocarcinoma), 종자세포종(germinoma 등이 있다. 치료는 수술적 치료가 선행되어야 하지만, 많이 진행되어 이미 다른 조직으로 전이가 이루어진 상태에서는 화학요법이 선택적으로 사용된다. |
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| 영문 | cancer | 한글 | 암 |
|---|---|---|---|
| 설명 | 끝없이 분열을 하여 혈액이나 림프관을 통하여 다른 장기에까지 전파될 수 있는 세포의 덩어리. 즉 악성 신생물을 말한다. 신생물은 악성과 양성이 있는데, 악성일 경우에는 성장이 매우 빠르고 혈액이나 림프관을 통해서 멀리 다른 떨어진 장기로 암세포의 전파가 가능하여 다른 장기에도 암을 전이하며, 양성은 천천히 자라고 다른곳으로 전이가 생기지 않는다. 암은 암종과 육종의 두 가지로 나눌 수가 있다. 암종이란 상피세포의 과도한 증식에 의한 악성신생물을 이르는 말이고 육종이란 비상피성세포 특히 중간엽세포(발생당시에 중간엽에 해당하는 조직으로 발생후에 조직사이에 분포하면서 조직을 지지하는 역할을 하는 결합조직, 혈관, 림프관 등이 된다)의 과도한 증식에 의한 악성 신생물을 이르는 말이다. |
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| AFP | Alpha(α) Feto-Protein [HP 1826, 1858, 1859, 2265] ; Oncofetal Antigens &nbs... |
|---|---|
| CEA | Carcino-Embryonic Antigen [HP 1825-6] ; Oncofetal Antigens ; Glycopro... |
| LC | Laennec cirrhosis; Langerhans cell; late clamped; large chromophobe; lecithin cholesterol acyltransf... |
| FHH | Familial Hypocalciuric Hypercalcemia = Familial Benign Hypercalcemia |
| FAD | familial Alzheimer dementia; familial autonomic dysfunction; fetal activity-acceleration determinati... |
| LC | Lung Cancer |
|---|---|
| LCSG | Lung Cancer Study Group |
| NSCLC | Non Small Cell Lung Cancer |
| SCLC | Small Cell Lung Cancer |
| BFNC | Benign Familial Neonatal Convulsions |
familial leiomyomatosis cutis et uteri (가족성 피부 자궁 근종증
| 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) |
|---|---|
| familial breast cancer | <oncology> 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. About15-20% 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. See related entries to: Breast cancer susceptibility genes; BRCA1; BRCA2. There are 2 genes; BRCA1 and BRCA2 which are susceptibility genes for breast cancer. They are inherited factors that predispose to breast cancer. Put otherwise, these genes make one more susceptible to the disease and so increase the risk of developing breast cancer. Two of these genes, BRCA1 and BRCA2, have been identified (and prominently publicised). Several other genes (those for the li-fraumeni syndrome, cowden disease, muir-torre syndrome, and ataxia-telangiectasia) are also known to predispose to breast cancer. However, since all of these known breast cancer susceptibility genes together do not account for more than a minor fraction (1/5th at most) of breast cancer that clusters in families, it is clear that more breast cancer genes remain to be discovered. (12 Dec 1998) |
| familial cancer | <oncology> One occurring in families more frequently than would be expected by chance. (09 Oct 1997) |
| cancer, lung | Cancer of the major organ of respiration the lung. Lung cancer kills more men and women than any other form of cancer. Since the majority of lung cancer is diagnosed at a relatively late stage, only 10% of all lung cancer patients are ultimately cured. Eight out of 10 lung cancers are due to tobacco smoke. Lung cancers are classified as either small cell or non-small cell cancers. Persistent cough and bloody sputum can be symptoms of lung cancer. Lung cancer can be diagnosed based on examination of sputum, or tissue examination with biopsy using bronchoscopy, needle through the chest wall, or surgical excision. (12 Dec 1998) |
| metastatic cancer to the lung | The spread of cancerous tumours from a distant organ to the lung. Due to the lungs tremendous blood and lymphatic supply it is a frequent site for metastatic cancer. Cancers which commonly metastasize to the lung include osteosarcoma, breast cancer, neuroblastoma, Wilm's tumour and non-Hodgkin's lymphomas. (27 Sep 1997) |
| metastatic lung cancer | The spread of cancerous tumours from a distant organ to the lung. Due to the lungs tremendous blood and lymphatic supply it is a frequent site for metastatic cancer. Cancers which commonly metastasize to the lung include osteosarcoma, breast cancer, neuroblastoma, Wilm's tumour and non-Hodgkin's lymphomas. (27 Sep 1997) |
| secondary lung cancer | The spread of cancerous tumours from a distant organ to the lung. Due to the lungs tremendous blood and lymphatic supply it is a frequent site for metastatic cancer. Cancers which commonly metastasize to the lung include osteosarcoma, breast cancer, neuroblastoma, Wilm's tumour and non-Hodgkin's lymphomas. (27 Sep 1997) |
| small cell lung cancer | A type of lung cancer in which the cells are small and round. Also called oat cell lung cancer. (12 Dec 1998) |
| nonsmall cell lung cancer | A general classification for squamous cell carcinoma, adenocarcinoma, and large cell carcinoma. (12 Dec 1998) |
| lung cancer | A cancerous growth in lung tissue. Lung cancer may be metastatic from another source (colon) or may be primary (tumour is of lung cell origin). Classification is based on the type of cell the lung cancer originates from (adenocarcinoma, alveolar cell carcinoma, squamous cell carcinoma, large cell and small cell carcinomas). (27 Sep 1997) |
| 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) |
| 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) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|