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| CFF | critical flicker fusion [test]; critical fusion frequency; cystic fibrosis factor; Cystic Fibrosis F... |
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| 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 |
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| ACKD | Acquired cystic kidney disease |
| ARCD | Acquired renal cystic disease |
| ACC | Adenoid Cystic Carcinoma |
| C.C.A.M. | Congenital Cystic Adenomatoid Malformation |
| cystic lymphangiectasis | A condition characterised by a fairly well circumscribed group of several or numerous, cystlike, dilated vessels or spaces lined with endothelium and filled with lymph. Synonym: cystic lymphangiectasis. (05 Mar 2000) |
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| cavernous lymphangiectasis | A condition of conspicuous dilation of lymphatic vessels in a fairly circumscribed region, frequently with the formation of cavities or "lakes" filled with lymph. Synonym: cavernous lymphangiectasis. (05 Mar 2000) |
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| simple lymphangiectasis | A circumscribed region or focus of several to numerous lymphatic vessels that are moderately dilated. Synonym: simple lymphangiectasis. (05 Mar 2000) |
| intestinal lymphangiectasis | Familial lymphangiectasis with intestinal loss of lymph causing lymphocytopenia and hypogammaglobulinaemia. (05 Mar 2000) |
| lymphangiectasis | Dilatation of the lymphatic vessels. (12 Dec 1998) |
| lymphangiectasis, intestinal | Dilatation of the intestinal lymphatic system, particularly in the lacteals in the intestinal villi, characterised by protein-losing enteropathy, steatorrhoea, and lymphopenia. It may be congenital, due to abnormality of the lymphatic system (as in milroy's disease) or acquired, due to involvement of the major intestinal lymphatic ducts by inflammatory processes or neoplasm, or to increased lymphatic pressure, as in valvular heart disease and constrictive pericarditis. (12 Dec 1998) |
| 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) |
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