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¿µ¹® cysticercosis ÇÑ±Û ³¶¹ÌÃæÁõ
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  °¥°í¸®ÃÌÃæ(Taenia solium)ÀÇ ¾Ö¹ú·¹°¡ Á¶Á÷³»¿¡ ±â»ýÇϴ º´À¸·Î ¿ì¸®³ª¶ó¿¡¼­ Á¶Á÷°Ë»ç¸¦ ÅëÇØ Áø´ÜµÇ´Â °¡Àå ÈçÇÑ ±â»ýÃæº´ÀÌ´Ù. ³¶¹ÌÃæÁõÀº °¥°í¸®ÃÌÃæÀÇ Ãæ¶õÀ» ¼·ÃëÇÑ ÈÄ, Ãæ¶õÀÌ ÀÛÀº Ã¢ÀÚ¿¡¼­ ºÎÈ­µÇ¾î À庮À» Ä§¹üÇϸç Ç÷·ù¸¦ ÅëÇØ ¾Ö¹ú·¹°¡ ÀÎüÁ¶Á÷³»¿¡¼­ ±â»ýÇÑ´Ù. µû¶ó¼­ ÀÎü°¡ ÀÏÁ¾ÀÇ Áß°£¼÷ÁÖÀÇ ¿ªÇÒÀ» Çϴ °¨¿° ÇüÅÂÀÌ´Ù. ÈçÇÑ ±â»ýºÎÀ§´Â ±ÙÀ° ÇǺιØÁ¶Á÷ ¹× ´«¾Ë, µå¹°°Ô Ã´¼ö¿¡ ±â»ýÇϱ⵵ ÇÑ´Ù. Á¶Á÷¿¡¼­ ÀÏÁ¾ÀÇ À°¾ÆÁ¶Á÷À¸·Î ±¸¼ºµÈ ³¶À» Çü¼ºÇÑ´Ù. ³ú³¶¹ÌÃæÁõÀǠħ¹üºÎÀ§´Â ¼ö¸·, ¹é»öÁú, È¸»öÁú, ³ú¼öÁ¶, ³ú½Ç µîÀÌ´Ù. º¸ÅëÀº À¯±¸³¶¹ÌÃæ(Cysticercus cellulosae)ÀÇ ÇüŸ¦ ÃëÇϳª °ø°£ÀÌ ³ÐÀº ºÎÀ§¿¡¼­´Â ³¶ÀÌ Æ÷µµ¼ÛÀÌó·³ º¸À̴ Æ÷µµ³¶¹ÌÃæ(Cysticercus racemosus)ÀÇ ÇüŸ¦ ÃëÇÑ´Ù.
  
  
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  • ¿µ¹®
    ÇѱÛ
  • 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 fibrosis
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  • cystic formation
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  • cystic goiter
    ³¶¼º°©»ó»ùÁ¾, ³¶¼º°©»ó¼±Á¾
  • cystic hygroma
    ³¶¸²ÇÁ°üÁ¾, ³¶¼ºÇÏÀ̱׷θ¶
  • cystic infarct
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  • cystic kidney
    ³¶¼ºÄáÆÏ, ³¶¼º½ÅÀå
  • cystic kidney disease
    ³¶¼ºÄáÆÏº´, ³¶¼º½ÅÀ庴
  • cystic lesion
    ³¶º´ÅÍ, ÁָӴϺ´ÅÍ
  • cystic lymphangioma
    ³¶¼º¸²ÇÁ°üÁ¾
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  • ¿µ¹®
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  • cystic lesion
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  • cystic medial necrosis
    ³¶¼ºÁßÃþ±«»ç
  • cystic neoplasm
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  • cystic teratoma
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  • cystic tumor
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  • cysticercosis
    ³¶¹ÌÃæÁõ
  • cysticercus
    ³¶¹ÌÃæ
  • cysticercus bovis
    ¹«±¸³¶¹ÌÃæ
  • cysticercus cellulosae
    À¯±¸³¶¹ÌÃæ
  • cysticercus viscerotropica
    ³»Àå³¶¹ÌÃæ
  • cystine
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  • cystinuria
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    ³¶Æ÷¿©µå¸§, ÁÖ¸Ó´Ï¿©µå¸§
  • cystic artery
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  • cystic bile
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  • cystic formation
    ³¶Çü¼º
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  • cystic hygroma
    ¸²ÇÁ¹°ÁÖ¸Ó´Ï
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    ÁÖ¸Ó´ÏÄáÆÏ, ³¶½ÅÀå
  • cystic kidney disease
    ÁÖ¸Ó´ÏÄáÆÏº´, ³¶¼º½ÅÀ庴
  • cystic liver
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  • cystic artery<³ª> arteria cystica
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    °£³¶¼ºÁúȯ(ÊÜÒ¥àõ òðü´).
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    ¾µ°³¸²ÇÁÀý
    [¿¾ ¿ë¾î] ´ã³¶ÀÓÆÄÀý
  • Cystic vein
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    [¿¾ ¿ë¾î] ´ã³¶Á¤¸Æ
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    Ò¥Ú­õùñø
  • cysticercus
    ³¶¹ÌÃæ
    Ò¥Ú­õù
  • Cysticercus cellulosae
    À¯±¸³¶¹ÌÃæ, À¯±¸³¶Ãæ
    êóÏ¢Ò¥Ú­õù, êóÏ¢Ò¥õù
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  • cysticercosis
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  • Cysticercus bovis
    ¹«±¸³¶¹ÌÃæ
  • Cysticercus cellulosae
    À¯±¸³¶¹ÌÃæ
  • Cysticercus fasciolaris
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  • Cysticercus racemosus
    Æ÷µµ³¶¹ÌÃæ
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    ¼¼°æ³¶Ãæ
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    ³»Àå³¶¹ÌÃæ
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  • cystic fibrosis
    ³¶¼º¼¶À¯Á¾
  • cystic kidney
    ³¶½Å
  • cystic lymphangioma
    ³¶¼º¸²ÇÁ°üÁ¾
  • cysticercosis
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  • cystis
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  • ÄÚµå
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    Cystic disease of liver
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    Cystic eyeball
    ³¶¼º ´«¾Ë(¾È±¸)
  • E84
    Cystic fibrosis
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    Cystic fibrosis with intestinal manifestations
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  • E84.8
    Cystic fibrosis with other manifestations
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  • cystic adenoma
    ³¶»ó ¼±Á¾
  • cystic degeneration
    ³¶»ó º¯¼º, ³¶Á¾ º¯¼º
  • cystic duct syndrome
    ´ã³¶ °ü ÁõÈıº
  • cystic epithelioma
    ³¶Æ÷¼º »óÇÇÁ¾
  • cystic fibrosis
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  • cystic kidney
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  • cystic neuroma
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  • cystic polyp
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  • cystic space
    ³¶Á¾»óÀÇ °ø°£
  • cysticercoid
    Àdz¶¹ÌÃæ
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    ´ã³¶ °ü³»ÀÇ °á¼®À» Á¦°ÅÇÏ´Â °Í.
  • cysticorrhaphy
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CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
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)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 1
  • Cystic Adenomatoid Malformation of Lung, Congenital - »õâ A developmental anomaly that usually becomes apparent in the neonatal period with progressive respiratory distress. This malformation is a focal pulmonary dysplasia characterized by a multicystic mass of terminal bronchiolar structures. CCAM is classified into 3 separate types (I, II, III) depending on cyst size.
    Synonyms : Congenital Cystic Adenomatoid Malformation of Lung, Cystic Adenomatoid Malformation of Lung, Lung Malformation, Congenital Cystic Adenomatoid, Lung Malformation, Cystic Adenomatoid, Congenital
  • Cystic Duct - »õâ The duct that is connected to the GALLBLADDER and allows the emptying of bile into the COMMON BILE DUCT.
    Synonyms : Cystic Ducts, Duct, Cystic, Ducts, Cystic
  • Cystic Fibrosis - »õâ An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.
    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
  • Cystic Fibrosis Transmembrane Conductance Regulator - »õâ A chloride channel that regulates secretion in many exocrine tissues. Abnormalities in the CFTR gene have been shown to cause cystic fibrosis. (Hum Genet 1994;93(4):364-8)
    Synonyms : Protein, CFTR
  • Cysticercosis - »õâ Infection with CYSTICERCUS, a larval form of the various tapeworms of the genus Taenia (usually T. solium in man). In humans they penetrate the intestinal wall and invade subcutaneous tissue, brain, eye, muscle, heart, liver, lung, and peritoneum. Brain involvement results in NEUROCYSTICERCOSIS. (From Dorland, 28th ed)
    Synonyms : Cysticercoses
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¿ÜºÎ ¸µÅ© - A.D.A.M. Medical Encyclopedia ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú: 10 ÆäÀÌÁö: 1
¿ÜºÎ ¸µÅ© - MedlinePlus Health Topics ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú: 2 ÆäÀÌÁö: 1
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cystic of or relating to a normal cyst (as the gallbladder or urinary bladder) of or relating to or resembling a cyst
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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
Ãâó: wordnet.princeton.edu/perl/webwn
cystic mastitis fibrocystic breast disease: the presence of one or more cysts in a breast
Ãâó: wordnet.princeton.edu/perl/webwn
cystine a crystalline amino acid found in proteins (especially keratin); discovered in bladder stones
Ãâó: wordnet.princeton.edu/perl/webwn
cystitis inflammation of the urinary bladder and ureters
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  • cystic fibrosis
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  • cysticercoid
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  • cysticercus
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  • cystiform
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  • cystine
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  • cystitis
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cysti of or relating to or resembling a cyst
cysti of or relating to a normal cyst (as the gallbladder or urinary bladder)
cysti a branch of the hepatic artery
cysti the presence of one or more cysts in a breast
cysti the most common congenital disease
cysti the presence of one or more cysts in a breast
cysti vein that drains the gallbladder
cysti a crystalline amino acid found in proteins (especially keratin)
cysti inflammation of the urinary bladder and ureters
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