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    ÇѱÛ
  • endomyocardial fibrosis
    ½É³»¸·½É±Ù¼¶À¯Áõ
  • fibrosis
    1. ¼¶À¯Áõ 2. ¼¶À¯È­
  • idiopathic pulmonary fibrosis
    Ư¹ßÆó¼¶À¯Áõ
  • idiopathic systemic fibrosis
    Ư¹ßÀü½Å¼¶À¯Áõ
  • interstitial fibrosis
    1. »çÀÌÁú¼¶À¯È­ 2. °£Áú¼¶À¯Áõ
  • mediastinal fibrosis
    Á¾°Ý¼¶À¯Áõ, ¼¼·ÎÄ­¼¶À¯Áõ
  • neoplastic fibrosis
    Á¾¾ç¼º¼¶À¯È­
  • postfibrinous fibrosis
    ¼¶À¯¼ÒÄ§ÂøÈļ¶À¯È­, ÇÇºê¸°Ä§ÂøÈļ¶À¯È­
  • periductal fibrosis
    °üÁÖÀ§¼¶À¯Áõ
  • reactive fibrosis
    ¹ÝÀÀ¼¶À¯È­
  • replacement fibrosis
    ´ëÄ¡¼¶À¯È­
  • subepidermal nodular fibrosis
    Ç¥ÇǹذáÀý¼¶À¯Áõ
  • submucous fibrosis
    Á¡¸·¹Ø¼¶À¯Áõ
  • sclerosing fibrosis
    °æÈ­¼¶À¯Áõ
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    ÇѱÛ
  • replacement fibrosis
    ´ëÄ¡¼¶À¯Áõ
  • sclerosing fibrosis
    °æÈ­¼¶À¯Áõ
  • subepidermal nodular fibrosis
    Ç¥ÇǹذáÀý¼¶À¯Áõ
  • submucous fibrosis
    Á¡¸·¹Ø¼¶À¯Áõ
  • proliferative inflammation
    Áõ½Ä¿°Áõ
  • proliferative retinopathy
    Áõ½Ä¸Á¸·º´Áõ
  • proliferative sparganosis
    Áõ½Ä½ºÆÄ¸£°¡´®Áõ, Áõ½Ä°íÃæÁõ
  • proliferative stage
    Áõ½Ä±â
  • proliferative state
    Áõ½Ä»óÅÂ
  • proliferative vitreoretinopathy
    Áõ½ÄÀ¯¸®Ã¼¸Á¸·º´Áõ
  • proliferative diabetic retinopathy
    Áõ½Ä´ç´¢¸Á¸·º´Áõ
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 2
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  • proliferative vitreoretinopathy
    Áõ½ÄÀ¯¸®Ã¼¸Á¸·º´Áõ
  • Cystic fibrosis
    ³¶¼º¼¶À¯Áõ(Òªàøàéë«ñø)
  • Fibrosis
    ¼¶À¯Áõ(àéë«ñø), ¼¶À¯È­(àéë«ûù)
  • Hamman Rich syndrome =diffuse interstitial pulmonary fibrosis
    ÇØ¸Õ- ¸®Ä¡ÁõÈıº.
  • arteriocapillary fibrosis
    µ¿¸Æ¸ð¼¼Ç÷°ü¼¶À¯Áõ(¡­Ù¾á¬úìηàéë«ñø).
  • hepatic fibrosis
    °£¼¶À¯Áõ(ÊÜàéë«ñø)
  • idiopathic pulmonary fibrosis
    Ư¹ß¼º Æó¼¶À¯È­Áõ(¡­øËàéë«ûùñø)
  • idiopathic systemic fibrosis
    Àü½Å¼º Ư¹ß¼º(îïãóàõ ÷åÛ¡àõ) ¼¶À¯Áõ
  • 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
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  • proliferative state
    Áõ½Ä»óÅÂ
  • proliferative vitreoretinopathy
    Áõ½ÄÀ¯¸®Ã¼¸Á¸·º´Áõ
  • arteriocapillary fibrosis
    µ¿¸Æ¸ð¼¼Ç÷°ü¼¶À¯Áõ(¡­Ù¾á¬úìηàéë«ñø).
  • circumscribed fibrosis
    ±¹ÇѼº ¼¶À¯Áõ
  • congenital fibrosis syndrome
    ¼±Ãµ¼¶À¯ÁõÁõÈıº
  • congenital hepatic fibrosis
    ¼±Ãµ¼º °£¼¶À¯Áõ(¡­ÊÜàéë«ñø).
  • corporal fibrosis
    (À½°æÇظé)ü ¼¶À¯Áõ(È­)
  • cortical stromal fibrosis
    ÇÇÁú°£Áú¼¶À¯È­(¡­Êàòõàéë«ûù)
  • cystic fibrosis
    ³¶¼º¼¶À¯Áõ(¡­àéë«ñø).
  • cystic fibrosis
    ³¶¼º¼¶À¯Áõ
  • cystic fibrosis
    ³¶¼º¼¶À¯Áõ(¡­àéë«ñø)
  • cystic fibrosis of pancreas
    ÃéÀå³¶¼º¼¶À¯Áõ(õýíôÒ¥àõàéë«ñø).
  • diffuse interstitial pulmonary fibrosis
    ¹Ì¸¸¼º °£Áú¼º Æó¼¶À¯Áõ.
  • endocardial fibrosis
    ½É³»¸·¼¶À¯Áõ.
  • endomyocardial fibrosis
    ½É³»¸·½É±Ù¼¶À¯Áõ.
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MPGN Mesangial(Membrano-) Proliferative Glomerulo-Nephritis
PDR Proliferative Diabetic Retinopathy; Áõ½Ä¼º ´ç´¢ ¸Á¸·Áõ
PPDR Pre-Proliferative Diabetic Retinopathy
AP accessory pathway; accounts payable; acid phosphatase; acinar parenchyma; action potential; active p...
BPL benign proliferative lesion; benzyl penicilloyl-polylysine; beta-propiolactone
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PPP Primary Proliferative Polycythaemia
PI Proliferative Index
PKD Proliferative Kidney Disease
PVR Proliferative Vitreoretinopathy
PA Proliferative activity
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mediastinal fibrosis <radiology> Histoplasmosis most common cause, can cause superior vena cava obstruction
(12 Dec 1998)
replacement fibrosis The formation of fibrous tissue that occupies sites where various other cells and tissues have become atrophied, or degenerated and necrotic.
(05 Mar 2000)
retroperitoneal fibrosis <radiology> Ureters tapered or obstructed, most severe at L4-5, ureters deviated medially, Treatment: symptomatic; steroids have ? long-term benefit Differential diagnosis: malignancy, lymphoma (especially Hodgkin's), metastasis from colon and breast, retroperitoneal sarcoma, drugs, methysergide (Sansert), haemorrhage, aortic aneurysm, trauma or surgery, inflammation, Crohn's disease, diverticulitis, pancreatitis, extravasated urine, radiation
(12 Dec 1998)
pericentral fibrosis Fibrosis occurring around the central veins in the hepatic lobules.
(05 Mar 2000)
perimuscular fibrosis Fibrosis in the outer media of arteries, usually the renal arteries of young women, where it causes segmental stenosis and hypertension; a variety of fibromuscular dysplasia.
Synonym: subadventitial fibrosis.
(05 Mar 2000)
pipestem fibrosis A characteristic pipe-shaped fibrosis formed around hepatic portal veins in some cases of long-continued heavy infection with Schistosoma mansoni; thought to be induced by the presence of large numbers of schistosome eggs in the hepatic tissues.
Synonym: Symmers' clay pipestem fibrosis, Symmers' fibrosis.
(05 Mar 2000)
congenital fibrosis of the extraocular muscles An autosomal dominant disorder associated with blepharoptosis and absence of eye movements.
(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)
progressive massive fibrosis <radiology> Progressive massive fibrosis, silicosis (properly conglomerate nodules, not progressive massive fibrosis), coal worker's pneumoconiosis, density (conglomerate mass) in upper lobe, retracts toward hilum, leaves emphysematous change (bullae) at lung periphery
(12 Dec 1998)
pulmonary fibrosis Chronic inflammation and progressive fibrosis of the pulmonary alveolar walls, with steadily progressive dyspnea, resulting finally in death from oxygen lack or right heart failure.
(12 Dec 1998)
subadventitial fibrosis Fibrosis in the outer media of arteries, usually the renal arteries of young women, where it causes segmental stenosis and hypertension; a variety of fibromuscular dysplasia.
Synonym: subadventitial fibrosis.
(05 Mar 2000)
nodular subepidermal fibrosis A slowly growing benign skin nodule consisting of poorly demarcated cellular fibrous tissue enclosing collapsed capillaries with scattered haemosiderin-pigmented and lipid macrophages. They are common, usually about 1 cm in diameter and occur in the dermis. Simple excision is always curative.
(12 Dec 1998)
Symmers' fibrosis A characteristic pipe-shaped fibrosis formed around hepatic portal veins in some cases of long-continued heavy infection with Schistosoma mansoni; thought to be induced by the presence of large numbers of schistosome eggs in the hepatic tissues.
Synonym: Symmers' clay pipestem fibrosis, Symmers' fibrosis.
(05 Mar 2000)
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