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  • ¿µ¹®
    ÇѱÛ
  • sclerosing fibrosis
    °æÈ­¼¶À¯Áõ
  • atypical cystic hyperplasia
    ºñÁ¤Çü³¶¼ºÁõ½Ä
  • acquired cystic kidney disease
    ÈÄõ³¶¼ºÄáÆÏº´, ÈÄõ³¶¼º½ÅÀ庴
  • adenoid cystic carcinoma
    »ù³¶¾ÏÁ¾, ¼±³¶¾ÏÁ¾
  • cystic
    ³¶-, ³¶Á¾-
  • cystic acne
    ³¶Æ÷¿©µå¸§, ÁÖ¸Ó´Ï¿©µå¸§
  • cystic artery
    ¾µ°³µ¿¸Æ, ´ã³¶µ¿¸Æ
  • cystic bile
    ¾µ°³¾µ°³Áó, ´ã³¶´ãÁó
  • cystic degeneration
    ³¶º¯¼º
  • cystic duct
    ¾µ°³ÁָӴϰü, ´ã³¶°ü
  • cystic formation
    ³¶Çü¼º
  • cystic goiter
    ³¶¼º°©»ó»ùÁ¾, ³¶¼º°©»ó¼±Á¾
  • cystic hygroma
    ³¶¸²ÇÁ°üÁ¾, ³¶¼ºÇÏÀ̱׷θ¶
  • cystic infarct
    ³¶¼º°æ»ö
  • cystic kidney
    ³¶¼ºÄáÆÏ, ³¶¼º½ÅÀå
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    ÇѱÛ
  • cystic acne
    ³¶Æ÷¿©µå¸§, ÁÖ¸Ó´Ï¿©µå¸§
  • cystic artery
    ¾µ°³µ¿¸Æ
  • benign cystic teratoma
    ¾ç¼º³¶±âÇüÁ¾
  • cystic bile
    ´ã³¶´ãÁó
  • cystic
    ³¶-, ³¶Á¾-
  • cystic degeneration
    ³¶º¯¼º
  • cystic formation
    ³¶Çü¼º
  • cystic goiter
    ³¶¼º°©»ó»ùÁ¾, ³¶¼º¹æÆÐ»ùÁ¾
  • cystic hygroma
    ¸²ÇÁ¹°ÁÖ¸Ó´Ï
  • cystic infarct
    ³¶¼º°æ»ö
  • cystic kidney
    ÁÖ¸Ó´ÏÄáÆÏ, ³¶½ÅÀå
  • cystic liver
    ³¶¼º°£, ¹°È¤°£
  • cystic mastitis
    ³¶¼ºÀ¯¹æ¿°
  • cystic mole
    (¢¡hydatid mole) Æ÷»ó±âÅÂ, Æ÷µµ¼ÛÀ̱âÅÂ
  • cystic ovary
    ³¶¼º³­¼Ò
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    ÇѱÛ
  • 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
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  • fibrosis,nodular subepidermal
    °áÀý¼º Ç¥ÇÇÇÏ
  • fibrosis,pipe-stem
    ÆÄÀÌÇÁ °ü
  • fibrosis,pulmonary, coal workers
    Æó, 걤ºÎ
  • fibrosis<³ª>
    ¼¶À¯Áõ(àéë«ñø), ¼¶À¯È­
  • hepatic fibrosis
    °£¼¶À¯Áõ(ÊÜàéë«ñø)
  • idiopathic diffuse intersitial fibrosis of lung
  • idiopathic pulmonary fibrosis
    Ư¹ß¼º Æó¼¶À¯È­Áõ(¡­øËàéë«ûùñø)
  • idiopathic systemic fibrosis
    Àü½Å¼º Ư¹ß¼º(îïãóàõ ÷åÛ¡àõ) ¼¶À¯Áõ
  • liver,pipe-stem fibrosis
    ÆÄÀÌÇÁ°ü¾ç ¼¶À¯È­(¡­Î·åÆ àéë«ûù)
  • myocardial fibrosis
    ½É±Ù¼¶À¯Áõ(¡­àéë«ñø).
  • myocardium,fibrosis
    ½É±Ù(ãýÐÉ), ¼¶À¯È­(àéë«ûù)
  • neoplastic fibrosis
    Á¾¾ç¼º ¼¶À¯Áõ(¡­àéë«ñø)
  • nodular subepidermal fibrosis
    °áÀý¼º Ç¥ÇÇÇÏ ¼¶À¯Áõ(¡­øúù«ù» àéë«ñø)
  • noncirrhotic portal fibrosis
    ºñ°æÈ­¼º ¹®¸Æ¼¶À¯Áõ.
  • noncirrhotic portal fibrosis
    ºñ°æÈ­¼º ¹®¸Æ¼¶À¯Áõ(ÞªÌãûùÚ¦Øæàéë«ñø)
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CF calcaneal fibular [ligament]; calcium leucovorin; calf blood flow; calibration factor; cancer-free; ...
CFAG cystic fibrosis antigen
CFFA cystic fibrosis factor activity
CFS cancer family syndrome; Chiari-Frommel syndrome; chronic fatigue syndrome; craniofacial stenosis; cr...
CFTR cystic fibrosis transmembrane conductance regulator
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
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
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    ¼³¸í
  • cystic epithelioma
    ³¶Æ÷¼º »óÇÇÁ¾
  • cystic kidney
    ³¶½Å
  • cystic lymphangioma
    ³¶¼º ¸²ÇÁ°üÁ¾
  • cystic neuroma
    ³¶¼º ½Å°æÁ¾
  • cystic polyp
    ³¶¼º Æú¸³
  • cystic space
    ³¶Á¾»óÀÇ °ø°£
  • fibrous cystic ostitis
    ³¶¼º ¼¶À¯¼º °ñ¿°
  • medullary cystic disease
    ¼öÁú³¶¼º Áúȯ
  • progressive cystic swelling
    ÁøÇ༺ ³¶Á¾¼º Á¾Ã¢
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
diffuse interstitial pulmonary fibrosis This represents a group of pulmonary disorders (lower respiratory tract) that leads to a functional loss in the alveolar air sacs and a compromise in the diffusion of oxygen from air to blood. There is widespread inflammation and scar tissue (fibrosis) formation within the lung. The causes are varied and include: inorganic and organic dusts, gases, fumes, vapors, infections, radiation, medications, coal dust, silicosis and byssinosis. When the cause is not identifiable it is referred to as idiopathic diffuse interstitial pulmonary fibrosis
(27 Sep 1997)
idiopathic interstitial fibrosis A progressive inflammatory condition starting with diffuse alveolar damage and resulting in fibrosis and honeycombing over a variable time period; also a common feature of collagen-vascular diseases.
Synonym: fibrosing alveolitis, Hamman-Rich syndrome, idiopathic interstitial fibrosis.
(05 Mar 2000)
idiopathic pulmonary fibrosis <radiology> Aka: usual interstitial pneumonia (UIP), 5-6th decade; M:F = 1:1, clubbing of fingers (83%), lymphocytosis on lavage, increased occurence of bronchogenic CA, average survival of 4-6 years; 87% mortality CXR findings: occasional ground glass pattern in early stage of alveolitis, diffuse reticulations (60%) predominantly at bases, honeycombing, pleural effusion (4%); pleural thickening (6%), pneumothorax in 7% (late stage), progressive volume loss see: interstitial pulmonary fibrosis
(12 Dec 1998)
interstitial pulmonary fibrosis <radiology> Idiopathic, idiopathic pulmonary fibrosis (AKA: usual interstitial pneumonitis), Hamman-Rich syndrome (rapidly progressive), drug-related, collagen-vascular disease, rheumatoid lung disease, scleroderma
(12 Dec 1998)
oral submucous fibrosis A precancerous condition of the oral mucosa and upper aerodigestive tract characteristically in a native of India.
(05 Mar 2000)
endocardial fibrosis Scarring or collaginosis of the endocardium.
Synonym: endocardial sclerosis.
(05 Mar 2000)
endomyocardial fibrosis A disease characterised by thickening of the endocardium, and frequently the inner third of the myocardium. The left ventricle is most frequently involved. Cardiomegaly and congestive heart failure may also be present.
(12 Dec 1998)
fibrosis The formation of fibrous tissue, fibroid or fibrous degeneration
(18 Nov 1997)
leptomeningeal fibrosis A fibrous reaction within the subarachnoid space; sometimes a sequel to infectious or chemical meningitis.
See: adhesive arachnoiditis.
(05 Mar 2000)
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)
KMLE À¥ ¿ë¾î ¸ÂÃã °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
cystic fibrosis an inherited disease in which a thick mucus clogs the lungs and blocks the ducts of the pancreas.
Ãâó: aspin.asu.edu/geneinfo/glos-c.htm
cystic fibrosis A common hereditary disease in which exocrine (secretory) glands produce abnormally thick mucus. This mucus can cause problems in digestion, breathing, and body cooling.
Ãâó: www.seniormag.com/conditions/cancer/cancerglossary...
cystic fibrosis a genetic disease transmitted by recessive inheritance. The disease is characterized by a buildup of mucus in the lungs and pancreatic insufficiency.
Ãâó: www.uvm.edu/~cgep/Education/Glossary.html
cystic fibrosis an inherited disorder of the exocrine glands, primarily the pancreas, pulmonary system and sweat glands, characterized by abnormally thick luminal secretions
Ãâó: depts.washington.edu/pwdlearn/web/glossary/glossar...
cystic fibrosis A common genetic disease. If both partners carry the gene, there is a 25% chance that the child will have the disease. This is unpleasant and currently there is no cure. It affects the lungs, bowels, pancreas, sweat glands etc.
Ãâó: www.ivf-infertility.com/help/glossary/abc.php
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