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"cystic lung"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • ¿µ¹®
    ÇѱÛ
  • 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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  • ¿µ¹®
    ÇѱÛ
  • cystic teratoma
    ³¶±âÇüÁ¾
  • cystic tumor
    ³¶Á¾
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  • ¿µ¹®
    ÇѱÛ
  • cystic mole
    (¢¡hydatid mole) Æ÷»ó±âÅÂ, Æ÷µµ¼ÛÀ̱âÅÂ
  • cystic ovary
    ³¶¼º³­¼Ò
  • 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
  • apex of lung
    ÇãÆÄ²À´ë±â, Æó²À´ë±â
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  • ¿µ¹®
    ÇѱÛ
  • artificial heart lung machine
    Àΰø½ÉÆó±â.
  • generalized obstructive lung disease
    ¹ü¹ß¼º Æó¼â¼º ÆóÁúȯ(ÛñÛ¡àõøÍáð
  • glass lung
    À¯¸®Æó.
  • heart lung machine
    (Àΰø)½ÉÆó±â, Àΰø½ÉÆóÀåÄ¡<±â>(ìÑÍïãýøËíûöÇ<Ðï>).
  • heart lung machine ; cardiopulmonary bypass machine
    ½ÉÆó±â.
  • heart lung preparation
    ½ÉÆóÇ¥º»(ãýøËøöÜâ).
  • heart lung ratio =HLR
    ½ÉÆó°è¼ö(ãýøËÌõâ¦), ½ÉÈä(°û)ºñ(ãýýØÎ¬Ýï).
  • heart-lung transplantation
    ½ÉÆóÀ̽Ä
  • hilum of lung
    Æó¹®(øËÚ¦).
  • honeycomb lung
    ¹úÁý¸ð¾çÆó, ºÀ¼Ò»óÆó
  • honycomb lung
    ¹úÁý¸ð¾çÆó
  • hydrostatic lung test
    ÆóºÎ¾ç½ÃÇè(øËݰåÖãËúÐ).
  • hypogenetic lung syndrome
    Àú¹ß»ý Æó ÁõÈıº
  • idiopathic unilateral hyperlucent lung
    Ư¹ß¼º ÀÏÃø¼º °úÅõ°ú¼ºÆó
  • imperfect lung aeration
    Æóȯ±âºÎÀü(øËüµÑ¨ÝÕîï).
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  • ¿µ¹®
    ÇѱÛ
  • cystic artery
    ´ã³¶µ¿¸Æ(ÓÅÒ¥ÔÑØæ)
  • cystic artery<³ª> arteria cystica
    ´ã³¶µ¿¸Æ(ÓÅÒ¥ÔÑØæ).
  • cystic artery<³ª> arteria cystica
    ´ã³¶µ¿¸Æ(´ã³¶µ¿¸Æ).
  • cystic atrophy
    ³¶¼ºÀ§Ãà(Ò¥àõê×õê)
  • cystic basal cell carcinoma
    ³¶Á¾¼º ±âÀú¼¼Æ÷¾Ï
  • cystic bile
    ³¶´ã(Ò¥ÓÅ).
  • cystic canal
    ´ã³¶°ü(´ã³¶°ü).
  • cystic cystitis<³ª> cystitis cystica
    ³¶¼º¹æ±¤¿°(¡­Û¹ÎÍæú).
  • cystic degeneration
    ³¶º¯¼º
  • cystic dermoid, teratoma
    ³¶¼º À¯ÇÇÁ¾(¡­ëºù«ðþ), ±âÇüÁ¾(ѱû¡ðþ)
  • cystic disease of liver
    °£³¶¼ºÁúȯ(ÊÜÒ¥àõ òðü´).
  • cystic disease of liver
    ³¶¼º°£Áúȯ(³¶¼º°£Áúȯ).
  • cystic duct
    ¾µ°³°ü
  • cystic duct
    ¾µ°³ÁָӴϰü
  • cystic duct syndrome
    ´ã³¶°üÁõÈıº(¡­ñøý¦ÏØ).
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  • ¿µ¹®
    ÇѱÛ
  • Right lung, middle lobe
    ¿À¸¥ÇãÆÄ, Áß°£¿±
    [¿¾ ¿ë¾î] ¿ìÆó, Áß¿±
  • Left lung, inferior lobe
    ¿ÞÇãÆÄ, ¾Æ·¡¿±
    [¿¾ ¿ë¾î] ÁÂÆó, ÇÏ¿±
  • Middle lobe (of right lung)
    Áß°£¿±(¿À¸¥ÇãÆÄ)
    [¿¾ ¿ë¾î] ¿ìÆóÁß¿±
  • Left lung
    ¿ÞÇãÆÄ
    [¿¾ ¿ë¾î] ÁÂÆó
  • Left lung, superior lobe
    ¿ÞÇãÆÄ, À§¿±
    [¿¾ ¿ë¾î] ÁÂÆó, »ó¿±
  • Lung
    ÇãÆÄ [Æó]
    [¿¾ ¿ë¾î] Æó
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    ÇѱÛ
  • lung
    ÆóÀå
  • lung biopsy
    Æó»ý°Ë
  • lung field
    Æó¾ß
  • lung marking
    Æó¹«´Ì
  • lung marking
    ÆóÀ½¿µ
  • middle lung field
    Á߯ó¾ß
  • open lung biopsy
    °³Èä»ý°Ë
  • radiation fibrosis of lung
    ¹æ»ç¼±Æó¼¶À¯Áõ
  • restrictive lung disease
    ±¸¼Ó¼ºÆóÁúȯ
  • upper lung field
    »óÆó±¸¿ª, »óÆó¾ß
  • wet lung
    ºÎÁ¾Æó, ½ÀÀ±Æó
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
CF   1) Cystic Fibrosis
  2) Complement Fixing antibody
  3) Conver...
PCK Poly-Cystic Kidney
PCO Poly-Cystic Ovary
PCOD Poly-Cystic Ovary Disease
  = Stein-Leventhal Syndrome
PCOS Poly-Cystic Ovary(Ovarian) Syndrome
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 2
C.C.A.M. Congenital Cystic Adenomatoid Malformation
CE Cystic Echinococcosis
CFTR Cystic Fibrosis Transmembrane Conductance Regulator
CFTR Cystic Fibrosis Transmembrane Conductance Regulator Gene
CFTR Cystic Fibrosis Transmembrane Regulator
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    ÇѱÛ
    ¼³¸í
  • fibrous cystic ostitis
    ³¶¼º ¼¶À¯¼º °ñ¿°
  • medullary cystic disease
    ¼öÁú³¶¼º Áúȯ
  • progressive cystic swelling
    ÁøÇ༺ ³¶Á¾¼º Á¾Ã¢
  • air-conditioner lung
    ¿¡¾îÄÜ Æó
  • apex of the lung
    Æó÷
    ÀüüÀûÀ¸·Î ¿øÃßÇüÀ» ÀÌ·é Æó ºÎÀ§ Áß »ÏÁ·ÇÑ À§ÂÊ ºÎÀ§.
  • arm to lung time test
    ÆÈ Æó ¼øÈ¯ ½Ã°£ ½ÃÇè
  • artificial heart lung apparatus
    Àΰø ½ÉÆó
  • cardiac lung
    ½É¼º Æó, ¿ïÇ÷ Æó
    ½ÉÀ庴 ƯÈ÷ ½Â¸ðÆÇ ÇùÂøÁõ ¶Ç´Â ÁÂ½É½Ç ºÎÀü¿¡ ÀÇÇÑ ÆóÀÇ ¸¸¼º ¿ïÇ÷.
  • drowned lung
    ÀÍ»çÀÚ Æó, ¼öÁ¾ Æó
  • electric lung
    Àü±â Æó
  • farmers lung
    ³óºÎ Æó
  • heart lung machine
    ½ÉÆó±â, Àΰø ½ÉÆó ÀåÄ¡±â
    µ¿¸Æ ÆßÇÁ. Ç÷¾×À» »ê¼Ò·Î Æ÷È­Çϱâ À§ÇÑ ÀåÄ¡·Î µ¿¸Æ ÆßÇÁ ¹× ¿©°ú±â¿Í Àú·ùÁ¶°¡ ºÙÀº Ç÷¾× ÇÊÅÍ¿Í Àú·ùÁ¶·Î ÀÌ·ç¾îÁø ±â±¸·Î, ü¿Ü ¼øÈ¯À¸·Î¼­, ½ÉÀå ¼ö¼úÀÇ °æ¿ì¿¡ ½ÉÀå°ú ÆóÀÇ ±â´ÉÀ» ´ëÇàÇϱâ À§ÇÏ¿© »ç¿ëÇÑ´Ù.
  • hypogenetic lung syndrome
    Àú¹ß»ý Æó ÁõÈıº
  • independent lung ventilation
    ºÐ¸® Æóȯ±â ¸¶Ãë
  • lingula of lung
    Æó ¼Ò¼³
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
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)
cystic gall duct The ductus leading from the gallbladder; it joins the hepatic duct to form the common bile duct.
Synonym: ductus cysticus.
(05 Mar 2000)
cystic goiter An enlargement in the thyroid region due to the presence of one or more cysts within the gland.
(05 Mar 2000)
cystic hygroma <radiology> Multiple cystic structures in nuchal region, lack of communication btw cervical lymphatics and venous system, unlike encephalocele: no cranial defect, no vertebral anomaly associated with: Turner syndrome, Roberts syndrome (single-gene disorder), Down syndrome
(12 Dec 1998)
cystic hyperplasia Formation of multiple retention cysts from obstruction of ducts or glands by hyperplasia of the lining epithelium, as in fibrocystic disease of the breast and metropathia haemorrhagica.
(05 Mar 2000)
cystic hyperplasia of the breast A benign disease common in women of the third, fourth, and fifth decades characterised by formation, in one or both breasts, of small cysts containing fluid which may appear as blue dome cysts; associated with stromal fibrosis and with variable degrees of intraductal epithelial hyperplasia and sclerosing adenosis.
Synonym: cystic hyperplasia of the breast.
(05 Mar 2000)
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