| ¿µ¹® | edema | ÇÑ±Û | ºÎÁ¾ |
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| ¼³¸í | Á¶Á÷³»¿¡ ¸²ÇÁ¾×À̳ª Á¶Á÷ÀÇ »ïÃâ¹° µîÀÇ ¾×ü°¡ Àú·ùµÇ¾î¼ °úÀ× Á¸ÀçÇÏ´Â »óŸ¦ ¸»ÇÑ´Ù. ÀÌ·± Çö»óÀº »ý±â´Â ºÎÀ§¿¡ µû¶ó ÇÇÇϺÎÁ¾, ÆóºÎÁ¾, º¹¼ö¶ó Çϸç, ¹ß»ý ±âÀü¿¡ µû¶ó ºÐ·ùÇÏ¸é ¿ïÇ÷¼º ºÎÁ¾, ¿°Áõ¼º ºÎÁ¾, Ç÷°ü¿îµ¿¼º ºÎÁ¾, ±â¾Æ¼º ºÎÁ¾, ÄáÆÏÅ¿ ºÎÁ¾ µîÀ¸·Î ºÐ·ùµÈ´Ù. ¿ïÇ÷¼º ºÎÁ¾Àº ±â´É¼º ºÎÁ¾À̶ó°íµµ Çϸç, Á¤¸ÆÀ̳ª ¸²ÇÁ°üÀÇ ÇùÂø, Æó¼â·Î ÀÎÇÏ¿© Á¤»óÀûÀÎ È帧ÀÌ ¹æÇع޾ÒÀ» ¶§¿¡ ¹ß»ýÇÏ´Â °ÍÀÌ´Ù. ¿°Áõ¼º ºÎÁ¾Àº ¿°Áõ¼º º¯È·Î ÀÎÇØ¼ Ç÷°üÀÇ Åõ°ú¼ºÀÌ Ç×ÁøµÇ¾î Ç÷°ü¼Ó¿¡ ÀÖ´Â ¼öºÐÀÌ ¸¹ÀÌ Á¶Á÷À¸·Î ºüÁ® ³ª°¡¼ »ý±â´Â ºÎÁ¾À̰í, Ç÷°ü¿îµ¿¼º ºÎÁ¾Àº Ç÷°ü¿îµ¿½Å°æ ¸¶ºñ·Î À¯¹ßµÇ¸ç, ±â¾Æ¼º ºÎÁ¾Àº ¸¸¼ºÀûÀ¸·Î ¿µ¾çÀÌ ºÎÁ·ÇÑ °æ¿ì¿¡ »ý±â´Â ºÎÁ¾ÀÌ´Ù. ÄáÆÏÅ¿ ºÎÁ¾Àº ÄáÆÏº´ÀÌ ÀÖ´Â °æ¿ì¿¡ ¼Òº¯À¸·Î ¿µ¾çºÐÀÌ ºüÁ®³ª°¡´Â °æ¿ì¿¡ À¯¹ßµÈ´Ù. ºÎÁ¾Àº »ý±â´Â ºÎÀ§¿¡ µû¶ó ´Ù¼Ò Â÷À̰¡ ÀÖÀ»Áö¶óµµ ¹ß»ý±âÀü¿¡¼´Â ¼·Î ¹ÐÁ¢ÇÑ °ü·ÃÀ» ¸Î°í ÀÖÀ¸¹Ç·Î ±Ùº»ÀûÀÎ ¿øÀÎÀ» ã¾Æ³»¾î Ä¡·á¸¦ ½ÃÀÛÇÏ´Â °ÍÀÌ ¹Ù¶÷Á÷ÇÏ´Ù. |
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| ¿µ¹® | interstitial therapy | ÇÑ±Û | ±ÙÁ¢Ä¡·á |
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| ¼³¸í | ÁÖ·Î Á¾¾çÀÇ Ä¡·á¸¦ ¸ñÀûÀ¸·Î ÇÏ¿© ÀÎü Á¶Á÷³»¿¡ ¹æ»ç¼± ¹°ÁúÀ» »ðÀÔÇÏ¿© ¹æ»ç¼±À» Á¶»çÇÏ´Â Ä¡·á¹ýÀÌ´Ù. Brachytherapy¶ó°íµµ ÇÑ´Ù. |
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| ¿µ¹® | nephritis(interstitial) | ÇÑ±Û | ÄáÆÏ¿°, ½ÅÀå¿°(°£Áú¼º) |
|---|---|---|---|
| ¼³¸í | ÄáÆÏ»çÀÌÁú(renal interstitium: ÄáÆÏÀÇ ¼¼´¢°ü »çÀÌÀÇ °áÇÕÁ¶Á÷)ÀÇ ¿°Áõ. ±Þ¼ºÀ¸·Î ÀϾ´Â °£ÁúÄáÆÏ¿°Àº ´ë°³ ¸¹Àº ¾àÀ» º¹¿ëÇÑ ÈÄ¿¡ ¹ß»ýÇÏ´Â µ¥, ¿, ÇǺÎÀÇ º¯»ö, Ç÷¾×³»ÀÇ È£»ê±¸Áõ ±×¸®°í ¼Òº¯ÀÇ °¨¼Ò¿Í ÄáÆÏ±â´ÉÀÇ °¨¼Ò¸¦ Ư¡À¸·Î ÇÑ´Ù. Ä¡·á´Â º¹¿ëÁßÀÎ ¾àÀ» ²÷°í, ºÎ½Å°ÑÁúÈ£¸£¸óÁ¦¸¦ Åõ¿©ÇÑ´Ù. ÄáÆÏÀº °¢Á¾ ³ëÆó¹°, ÀüÇØÁú, ¼öºÐ µîÀ» Æ÷ÇÔÇÑ ¿ä¸¦ »ý»êÇÏ¿© ¹èÃâÇÏ´Â µ¿½Ã¿¡ ¼ö¼ÒÀÌ¿Â, ³ªÆ®·ý, Ä®·ý, Àλê À̿ ³óµµ µîÀ» Á¶ÀýÇÏ¸ç ³»ºÐºñ¿Í ¿ÜºÐºñ ±â´É¿¡ °ü¿©Çϱ⵵ ÇÑ´Ù. |
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| HPE | hepatic portoenterostomy; high-permeability edema; history and physical examination; holoprosencepha... |
|---|---|
| ILP | inadequate luteal phase; insufficiency of luteal phase; interstitial laser photocoagulation; interst... |
| EF | Edema Factor |
| HACE | High Altitude Cerebral Edema |
| HAPE | High Altitude Pulmonary Edema |
| BE | Brain edema |
|---|---|
| CSME | Clinically significant macular edema |
| CME | Cystoid macular edema |
| EPH | Edema Proteinuria Hypertension |
| HANE | Hereditary Angio Neurotic Edema |
| edema | <clinical sign> The presence of abnormally large amounts of fluid in the intercellular tissue spaces of the body, usually applied to demonstrable accumulation of excessive fluid in the subcutaneous tissues. Oedema may be localised, due to venous or lymphatic obstruction or to increased vascular permeability or it may be systemic due to heart failure or renal disease. Collections of oedema fluid are designated according to the site, for example ascites (peritoneal cavity), hydrothorax (pleural cavity) and hydropericardium (pericardial sac). Massive generalised oedema is called anasarca. Origin: Gr. Oide ma = swelling (18 Nov 1997) |
|---|---|
| edema, cardiac | A manifestation of congestive heart failure caused by increased venous and capillary pressures and often associated with the retention of sodium by the kidneys. (12 Dec 1998) |
| acute interstitial nephritis | <nephrology> A relatively uncommon condition which is characterised by inflammation of the renal tubules, glomeruli and surrounding tissue. Interstitial nephritis is usually be temporary and often associated with the use of a particular medication. Chronic and progressive forms do exist. Drugs that have been associated with interstitial nephritis include penicillins, ampicillin, sulpha drugs, non-steroidal anti-inflammatory agents, furosemide and thiazide diuretics. May result in mild kidney dysfunction or acute renal failure. Treatment may be with corticosteroids. Incidence: 1 in 25,000. (29 Dec 1997) |
| acute interstitial pneumonia | A severe and usually fatal form of pneumonia occurring primarily in infants usually considered a form of hypersensitivity pneumonitis. (05 Mar 2000) |
| acute interstitial pneumonitis | Usually considered a form of hypersensitivity pneumonitis. (05 Mar 2000) |
| apical interstitial lung disease | <radiology> A radiological diagnosis where fibrosis is seen in the apices (upper sections) of the lungs. Likely causes include: cystic fibrosis, ankylosing spondylitis, sarcoidosis, silicosis, eosinophlic granuloma, TB and fungus, particularly aspergillus infection. (25 Jun 1999) |
| basilar interstitial lung disease | <radiology> B bronchiectasis, A asbestosis, D drugs / DIP, L lymphangitic metastasis / LAM, A aspiration, S sarcoidosis, S scleroderma (12 Dec 1998) |
| chronic interstitial hepatitis | An obsolete term for cirrhosis of the liver. (05 Mar 2000) |
| chronic interstitial hypertrophic neuropathy | dejerine-Sottas disease |
| chronic interstitial salpingitis | Salpingitis in which fibrosis or mononuclear cell infiltration involves all layers of the fallopian or eustachian tube. Synonym: pachysalpingitis. (05 Mar 2000) |
| pneumonia, atypical interstitial, of cattle | A cattle disease of uncertain cause, probably an allergic reaction. (12 Dec 1998) |
| pneumonia, progressive interstitial, of sheep | Chronic respiratory disease caused by the visna-maedi virus. It was formerly believed to be identical with jaagsiekte (pulmonary adenomatosis, ovine) but is now recognised as a separate entity. (12 Dec 1998) |
| cystitis, interstitial | Disease that involves inflammation or irritation of the bladder wall. This inflammation can lead to scarring and stiffening of the bladder, and even ulcerations and bleeding. Diagnosis is based on symptoms, findings on cystoscopy and biopsy, and eliminating other treatable causes such as infection. Because doctors do not know what causes IC, treatments are aimed at relieving symptoms. most people are helped for variable periods of time by one or a combination of treatments. (12 Dec 1998) |
| hypertrophic interstitial neuropathy | Sensorimotor neuropathy characterised pathologically by collections of Schwann cell processes arranged concentrically around one or more nerve fibres. No genetic factors are known in its aetiology.For hereditary types, see hereditary hypertrophic neuropathy. (05 Mar 2000) |
| nephritis, interstitial | Primary or secondary disease of the renal interstitial tissue resulting from arterial, arteriolar, glomerular, or tubular disease which destroys individual nephrons, or from toxic involvement of interstitital cells and tubules due to systemic diseases such as gout, to drug exposure, or to mercury poisoning. Clinically it may be manifested primarily by loss of concentrating capacity, mineral wasting, proteinuria, and abnormal urine sediment. It may be seen in an acute form, particularly after specific bacterial infection, and may result in acute papillary necrosis. More commonly, the process is a chronic one with progressive renal atrophy and diminution of renal function. (12 Dec 1998) |
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