| 영문 | cystic fibrosis | 한글 | 낭성섬유증 |
|---|---|---|---|
| 설명 | 유전병의 하나로 땀샘, 기관지에서 점액을 분비하는 샘, 이자등의 외분비샘(몸 밖으로 액체를 분비하는 샘. 내분비샘을 제외한 모든 샘을 이른다)의 이상을 특징으로 하는 병이다. 중요한 병적인 변화는 주로 기관지에서 점액을 분비하는 분비샘에서 지나치게 점도가 높은 점액이 분비되어 기관지를 막아 호흡장애를 일으키는 폐의 병터이며, 땀에서 과도한 전해질 특히 염화나트륨(NaCl)이 분비되어 몸에 전해질이 부족하게 된다. 또 이자의 소화액을 분비하는 분비샘의 이상으로 이자관이 막히거나 이자의 기능이 떨어져서 소화의 장애를 일으키기도 한다. 유태계에 많으며 우리나라에는 아주 드물다. |
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| 영문 | cysticercosis | 한글 | 낭미충증 |
|---|---|---|---|
| 설명 | 갈고리촌충(Taenia solium)의 애벌레가 조직내에 기생하는 병으로 우리나라에서 조직검사를 통해 진단되는 가장 흔한 기생충병이다. 낭미충증은 갈고리촌충의 충란을 섭취한 후, 충란이 작은 창자에서 부화되어 장벽을 침범하며 혈류를 통해 애벌레가 인체조직내에서 기생한다. 따라서 인체가 일종의 중간숙주의 역할을 하는 감염 형태이다. 흔한 기생부위는 근육 피부밑조직 및 눈알, 드물게 척수에 기생하기도 한다. 조직에서 일종의 육아조직으로 구성된 낭을 형성한다. 뇌낭미충증의 침범부위는 수막, 백색질, 회색질, 뇌수조, 뇌실 등이다. 보통은 유구낭미충(Cysticercus cellulosae)의 형태를 취하나 공간이 넓은 부위에서는 낭이 포도송이처럼 보이는 포도낭미충(Cysticercus racemosus)의 형태를 취한다. |
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| 영문 | cystic fibrosis | 한글 | 낭성섬유증 |
|---|---|---|---|
| 설명 | 유전병의 하나로 땀샘, 기관지에서 점액을 분비하는 샘, 이자등의 외분비샘(몸 밖으로 액체를 분비하는 샘. 내분비샘을 제외한 모든 샘을 이른다)의 이상을 특징으로 하는 병이다. 중요한 병적인 변화는 주로 기관지에서 점액을 분비하는 분비샘에서 지나치게 점도가 높은 점액이 분비되어 기관지를 막아 호흡장애를 일으키는 폐의 병터이며, 땀에서 과도한 전해질 특히 염화나트륨(NaCl)이 분비되어 몸에 전해질이 부족하게 된다. 또 이자의 소화액을 분비하는 분비샘의 이상으로 이자관이 막히거나 이자의 기능이 떨어져서 소화의 장애를 일으키기도 한다. 유태계에 많으며 우리나라에는 아주 드물다. |
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| CFF | critical flicker fusion [test]; critical fusion frequency; cystic fibrosis factor; Cystic Fibrosis F... |
|---|---|
| CFP | chronic false positive; Clinical Fellowship Program; cyclophosphamide, fluorouracil, prednisone; cys... |
| CF | 1) Cystic Fibrosis 2) Complement Fixing antibody 3) Conver... |
| PCK | Poly-Cystic Kidney |
| PCO | Poly-Cystic Ovary |
| ACDK | Acquired cystic disease of the kidney |
|---|---|
| ACKD | Acquired cystic kidney disease |
| ARCD | Acquired renal cystic disease |
| ACC | Adenoid Cystic Carcinoma |
| C.C.A.M. | Congenital Cystic Adenomatoid Malformation |
| cystic | 1. Relating to the urinary bladder or gallbladder. 2. Relating to a cyst. 3. Containing cysts. Synonym: cystous. (05 Mar 2000) |
|---|---|
| cystic acne | <dermatology> A form of acne which results from the bacterial infection of cysts deep within the skin. Generally requires treatment with antibiotics and other agents (Isotretinoin). Without treatment cystic acne may result in scarring. (27 Sep 1997) |
| cystic adenomatoid malformation of lung | <radiology> Only true pulmonary cystic disease of newborn, three X-ray types: multicystic, walls of varying thickness, multicystic, one large dominant thin-walled cyst, solid, mediastinal shift common, cysts often contain foetal lung fluid, Treatment: surgery Cf: congenital lobar emphysema (12 Dec 1998) |
| cystic adenomatoid malformation of lung, congenital | A developmental anomaly that usually becomes apparent in the neonatal period with progressive respiratory distress. This malformation is a focal pulmonary dysplasia characterised by a multicystic mass of terminal bronchiolar structures. Ccam is classified into 3 separate types (I, II, III) depending on cyst size. (12 Dec 1998) |
| cystic adnexal masses | <radiology> Ovarian cyst, mature follicle measures up to 2.5 cm at ovulation, corpus luteum cyst common in first 16 weeks of pregnancy, polycystic (Stein-Leventhal) disease, paraovarian cyst, Wolffian duct remnants in broad ligament, ovarian neoplasm, serous cystadenoma (most common benign ovarian tumour), mucinous cystadenoma (usually complex), cystic teratoma (usually complex), endometriosis, diffuse (not detectable by ultrasound), localised (generally anechoic or hypoechoic), ectopic pregnancy, pelvic inflammatory disease, gonorrhoea or chlamydia, localised abscess and hydrosalpinx, non-gynecologic mass, mesenteric cyst, ureterocele, bladder diverticula, lymphocele (12 Dec 1998) |
| cystic artery | <anatomy, artery> Origin, right branch of hepatic; distribution, gall bladder and visceral surface of the liver. Synonym: arteria cystica. (05 Mar 2000) |
| cystic bronchiectasis | Bronchiectasis in which the bronchi end in blind sacs greater in diameter than the draining bronchi. See: saccular bronchiectasis. (05 Mar 2000) |
| cystic carcinoma | <tumour> A carcinoma in which true epithelium-lined cysts are formed, or degenerative changes may result in cystlike spaces. (05 Mar 2000) |
| cystic diathesis | A condition in which multiple cysts form in the liver, kidneys, and other organs. (05 Mar 2000) |
| cystic disease of renal medulla | Presence of small cysts in the renal medulla associated with anaemia, sodium depletion, and chronic renal failure. It is of two types: 1) fatal autosomal recessive or juvenile type (also called familial juvenile nephrophthisis), beginning at about age 10 with an average duration of 6 to 8 years; 2) autosomal dominant or adult type, beginning at about age 30 but with a more fulminant course. Synonym: microcystic disease of renal medulla. (05 Mar 2000) |
| cystic duct | <anatomy> A bile duct that connects the gallbladder to the common bile duct. A gallstone that blocks the cystic duct can lead to inflammation and infection of the gallbladder. See: common bile duct. (27 Sep 1997) |
| cystic duct cholangiography | Radiography of the biliary system after introduction of contrast medium through the cystic duct. (05 Mar 2000) |
| cystic fibrosis | <chest medicine> A generalised disorder of infants, children and young adults, in which there is widespread dysfunction of the exocrine glands, characterised by signs of chronic pulmonary disease (due to excess mucus production in the respiratory tract), pancreatic deficiency, abnormally high levels of electrolytes in the sweat and occasionally by biliary cirrhosis. There is an ineffective immunologic defense against bacteria in the lungs. Pathologically, the pancreas shows obstruction of the pancreatic ducts by amorphous eosinophilic concretions, with consequent deficiency of pancreatic enzymes, resulting in steatorrhoea and azotorrhoea and intestinal malabsorption. The degree of involvement of organs and glandular systems may vary greatly, with consequent variations in the clinical picture. Inheritance: autosomal recessive. (13 Nov 1997) |
| cystic fibrosis antigen | Now known to be MRP 8. See: calgranulins. (18 Nov 1997) |
| cystic fibrosis transmembrane conductance regulator | Gene believed to be defective in cystic fibrosis. Gene encodes a chloride channel, homologous to a family of proteins that actively transport small solutes in an ATP dependent manner (ABC transporters). The regulator protein is a protein which is embedded in the cell membrane and acts as a channel for certain ions to be transported into or out of the cell. The disease cystic fibrosis is caused by a defect in the gene for this protein. (09 Oct 1997) |
| adenoid cystic carcinoma | <tumour> A histologic type of carcinoma characterised by large epithelial masses containing round, glandlike spaces or cysts which frequently contain mucus or collagen and are bordered by a few or many layers of epithelial cells without intervening stroma, forming a cribriform pattern like a slice of Swiss cheese; perineural invasion and haematogenous metastasis are common; occurs most commonly in salivary glands. Synonym: cylindromatous carcinoma. (05 Mar 2000) |
|---|---|
| carcinoma, adenoid cystic | Carcinoma characterised by bands or cylinders of hyalinised or mucinous stroma separating or surrounded by nests or cords of small epithelial cells. When the cylinders occur within masses of epithelial cells, they give the tissue a perforated, sievelike, or cribriform appearance. Such tumours occur in the mammary glands, the mucous glands of the upper and lower respiratory tract, and the salivary glands. They are malignant but slow-growing, and tend to spread locally via the nerves. (12 Dec 1998) |
| pancreatic cystic neoplasms | <radiology> Microcystic adenoma, glycogen, benign, mucinous cystic neoplasm, macrocystic adenoma, cystadenoma/cystadenocarcinoma, mucin, pre-malignant, Both occur more commonly in women, peak in middle age (12 Dec 1998) |
| papillary cystic adenoma | <tumour> An adenoma in which the lumens of the acini are frequently distended by fluid, and the neoplastic epithelial elements tend to form irregular, fingerlike projections. (05 Mar 2000) |
| medullary cystic disease | <disease> A rare hereditary kidney disease characterised by the gradual loss of kidney function due to the presence of cysts in the renal medulla. Symptoms include high urine output (cannot concentrate the urine), weakness, weight loss, nocturia, fatigue and headache. There is no cure and usually progresses from chronic renal failure to end stage renal disease. (27 Sep 1997) |
| medullary cystic kidney disease | <radiology> Mode of inheritance uncertain, usually affects young adults (early 20s), associated with red or blond hair (!!), causes salt wasting, polyuria, azotaemia, affects both kidneys, with progressive disease patients need dialysis or transplant (12 Dec 1998) |
| mesothelioma, cystic | A peritoneal mesothelioma affecting mainly young females and producing cysts of variable size and number lined by a single layer of benign mesothelial cells. The disease follows a benign course and is compatible with a normal life expectancy, requiring occasionally partial excision or decompression for relief of pain or other symptoms. Malignant potential is exceptional. (12 Dec 1998) |
| chronic cystic mastitis | Older term corresponding to fibrocystic condition of the breast. (05 Mar 2000) |
| mucinous cystic neoplasm of pancreas | <radiology> = macrocystic adenoma of pancreas, cystadenoma / cystadenocarcinoma, M:F = 1:9, 40-60 years of age, malignant or pre-malignant, large mass (mean 12 cm), multilocular cysts, thick septations, tail / body in 85% (unlike adenocarcinoma and microcystic adenoma), hypo-/avascular, Differential diagnosis: panc pseudocyst, ** Cf: microcystic adenoma (12 Dec 1998) |
| multilocular cystic nephroma | <radiology> Cystic hamartoma, cystadenoma, congenital, usually benign, multiple small, noncommunicating cysts in single renal mass, usually large (mean 10 cm), with or without calcification, 50% detected in childhood, remainder in older adults, kids: M more than F, adults: F more than M (12 Dec 1998) |
| spiral fold of cystic duct | A series of crescentic folds of mucous membrane in the upper part of the cystic duct, arranged in a somewhat spiral manner. Synonym: plica spiralis ductus cystici, Amussat's valve, Heister's valve, spiral valve of cystic duct, valvula spiralis. (05 Mar 2000) |
| spiral valve of cystic duct | A series of crescentic folds of mucous membrane in the upper part of the cystic duct, arranged in a somewhat spiral manner. Synonym: plica spiralis ductus cystici, Amussat's valve, Heister's valve, spiral valve of cystic duct, valvula spiralis. (05 Mar 2000) |
| neoplasms, cystic, mucinous, and serous | Neoplasms containing cyst-like formations or producing mucin or serum. (12 Dec 1998) |
| ovarian cystic disease | <gynaecology> A painful condition associated with the recurrent formation of large ovarian cysts. Distention of the ovarian capsule causes pain and rupture of a larger cyst can, in rare instances, cause internal bleeding. Treatment often includes hormone manipulation (birth control pills). (05 Jan 1998) |
| kidney, cystic | A kidney containing one or more cysts, including polycystic disease (kidney, polycystic), solitary cyst, multiple simple cysts, and retention cysts (associated with parenchymal scarring). (12 Dec 1998) |
Synonyms : Congenital Cystic Adenomatoid Malformation of Lung, Cystic Adenomatoid Malformation of Lung, Lung Malformation, Congenital Cystic Adenomatoid, Lung Malformation, Cystic Adenomatoid, Congenital
Synonyms : Cystic Ducts, Duct, Cystic, Ducts, Cystic
Synonyms : Fibrocystic Disease of Pancreas, Pancreatic Cystic Fibrosis, Pulmonary Cystic Fibrosis, Cystic Fibrosis, Pancreatic, Cystic Fibrosis, Pulmonary, Fibrosis, Cystic, Pancreas Fibrocystic Disease, Pancreas Fibrocystic Diseases
Synonyms : Protein, CFTR
Synonyms : Cysticercoses
| cystic |
of or relating to a normal cyst (as the gallbladder or urinary bladder) of or relating to or resembling a cyst
출처: wordnet.princeton.edu/perl/webwn
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|---|---|
| cystic fibrosis |
the most common congenital disease; the child's lungs and intestines and pancreas become clogged with thick mucus; caused by defect in a single gene; there is no cure
출처: wordnet.princeton.edu/perl/webwn
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| cystic mastitis |
fibrocystic breast disease: the presence of one or more cysts in a breast
출처: wordnet.princeton.edu/perl/webwn
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| cystic artery |
a branch of the hepatic artery; supplies the gall bladder and the surface of the liver
출처: wordnet.princeton.edu/perl/webwn
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| cystic vein |
vein that drains the gallbladder
출처: wordnet.princeton.edu/perl/webwn
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| cystic | of or relating to or resembling a cyst |
|---|---|
| cystic | of or relating to a normal cyst (as the gallbladder or urinary bladder) |
| cystic | a branch of the hepatic artery |
| cystic | the presence of one or more cysts in a breast |
| cystic | the most common congenital disease |
| cystic | the presence of one or more cysts in a breast |
| cystic | vein that drains the gallbladder |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|