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  • cystic kidney disease
    ³¶¼ºÄáÆÏº´, ³¶¼º½ÅÀ庴
  • cystic lesion
    ³¶º´ÅÍ, ÁָӴϺ´ÅÍ
  • cystic lymphangioma
    ³¶¼º¸²ÇÁ°üÁ¾
  • cystic mastitis
    ³¶¼ºÀ¯¹æ¿°
  • cystic medial necrosis
    ³¶¼ºÁß°£¸·±«»ç
  • cystic mole
    Æ÷»ó±âÅÂ
  • cystic neoplasm
    ³¶¼º½Å»ý¹°, ³¶¼ºÁ¾¾ç
  • cystic ovary
    ³¶¼º³­¼Ò
  • cystic polyp
    ³¶¼ºÆú¸³
  • cystic renal dysplasia
    ³¶¼ºÄáÆÏÇü¼ºÀÌ»ó, ³¶¼º½ÅÀåÇü¼ºÀÌ»ó
  • cystic teratoma
    ³¶¼º±âÇüÁ¾
  • cystic tumor
    ³¶¼ºÁ¾¾ç
  • medullary cystic disease
    ¼ÓÁú³¶º´, ¼öÁú³¶¼ºº´
  • solid-cystic tumor
    °íÇü³¶¼ºÁ¾¾ç
  • simple cystic kidney
    ´Ü¼ø³¶½ÅÀå, ȬÁÖ¸Ó´ÏÄáÆÏ
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    ÇѱÛ
  • cystic stone
    ¾µ°³µ¹, ´ã³¶µ¹
  • cystic teratoma
    ³¶±âÇüÁ¾
  • cystic encephalomalatic cavity
    ³¶Á¾³ú¿¬È­°øµ¿
  • cystic kidney disease
    ÁÖ¸Ó´ÏÄáÆÏº´, ³¶¼º½ÅÀ庴
  • cystic medial necrosis
    ³¶¼ºÁßÃþ±«»ç
  • cystic renal dysplasia
    ³¶¼ºÄáÆÏÇü¼ºÀÌ»ó, ³¶¼º½ÅÀåÇü¼ºÀÌ»ó
  • cystic renal medulla
    ÁÖ¸Ó´ÏÄáÆÏ¼ÓÁú, ÁָӴϽżöÁú
  • cystic retinal tuft
    ³¶Æ÷¸Á¸·¼ú
  • medullary cystic disease
    ¼ÓÁú³¶¼ºº´, ¼ÓÁúÁÖ¸Ó´ÏÄáÆÏº´
  • uremic medullary cystic disease
    ¿äµ¶¼ÓÁú³¶º´
  • simple cystic kidney
    ´Ü¼ø³¶ÄáÆÏ, ȬÁÖ¸Ó´ÏÄáÆÏ
  • solid-cystic tumor
    °íü³¶¼ºÁ¾¾ç
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  • pancreatic fibrosis
    Ã鼺¼¶À¯Áõ(õýàõàéë«ñø)
  • postfibrinous fibrosis
    Èļ¶À¯¼Ò¼º ¼¶À¯Áõ(ý­àéë«áÈàõ àéë«ñø)
  • preretinal fibrosis
    ¸Á¸·¾Õ¼¶À¯Áõ
  • preretinal macular fibrosis
    ¸Á¸·¾ÕȲ¹Ý¼¶À¯Áõ
  • progressive nodular fibrosis of the skin
    ÁøÇ༺ °áÀý ÇǺΠ¼¶À¯Áõ
  • pulmonary fibrosis
    Æó¼¶À¯Áõ(øËàéë«ñø).
  • pulmonary fibrosis
    Æó¼¶À¯Áõ(øËàéë«ñø)
  • pulmonary fibrosis
    Æó¼¶À¯È­
  • radiation fibrosis
    ¹æ»ç ¹æ»ç¼±¼¶À¯Áõ(Û¯ÞÒàÊ àéë«ñø).
  • radiation fibrosis
    ¹æ»ç¼± ¼¶À¯Áõ(Û¯ÞÒàÊ àéë«ñø)
  • radiation fibrosis
    ¹æ»ç¼±¼¶À¯Áõ
  • radiation fibrosis of lung
    ¹æ»ç¼±Æó¼¶À¯Áõ(Û¯ÞÒàÊøËàéë«ñø).
  • radiation fibrosis of lung
    ¹æ»ç¼±Æó¼¶À¯Áõ(Û¯ÞÒàÊøËàéë«ñø)
  • reactive fibrosis
    ¹ÝÀÀ¼º ¼¶À¯È­
  • replacement fibrosis
    ´ëÄ¡¼º ¼¶À¯Áõ(¡­àéë«ñø)
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ICF(M)A International Cystic Fibrosis (Mucoviscidosis) Association
IPF Idiopathic Pulmonary Fibrosis
PMF Progressive Massive Fibrosis
  = Silicosis
CHF chick embryo fibroblast; chronic heart failure; congenital hepatic fibrosis; congestive heart failur...
CIPF classic interstitial pneumonitis-fibrosis; clinical illness promoting factor
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 3
CCAM Congenital cystic adenomatoid malformation of the lung
CE Cystic Echinococcosis
CPDN Cystic partially differentiated nephroblastoma
GCDFP-15 Gross Cystic Disease Fluid Protein
GCDFP-15 Gross Cystic Disease Fluid Protein-15
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
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)
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)
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cystic fibrosis A chronic disease of the glands of secretion. It may seriously affect respiratory passages, pancreas and liver, and sweat glands.
Ãâó: www.usctransplant.org/heart/glossary.html
cystic fibrosis A recessive genetic disorder affecting the mucus lining of the lungs, leading to breathing problems and other difficulties.
Ãâó: www.ornl.gov/sci/techresources/Human_Genome/public...
cystic fibrosis This is an inherited disease of the exocrine glands affecting the lungs and the digestive systems. The lungs in these persons can become infected easily which may cause permanent damage to the alveoli, bronchioles and bronchi. Production of thick, sticky mucus blocks the airways and obstructs normal ventilation and function of the lungs.
Ãâó: www.iacpr.net/services/glossary_terms.php
cystic fibrosis A genetic disease involving a sticky buildup of mucus in the lungs (which makes breathing difficult and leads to infections), as well as pancreatic insufficiency (which leads to digestive problems). It is a recessive disease, occurring only when a child inherits two mutated copies of the CF gene--one from each parent.
Ãâó: www.med.nyu.edu/rcr/rcr/glossary.html
cystic fibrosis An inherited disease characterized by chronic respiratory and digestive problems.
Ãâó: chfs.ky.gov/dcbs/dpp/GLOSSARY+OF+ADOPTION+TERMS.ht...
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