| 영문 | renal biopsy | 한글 | 콩팥생검 |
|---|---|---|---|
| 설명 | 콩팥의 병변이 의심될 때 확진을 위해 주사바늘 등을 이용하여 콩팥조직을 일부 떼어내서 현미경으로 검경하는 것. |
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| 영문 | renal hypertension | 한글 | 콩팥성고혈압 |
|---|---|---|---|
| 설명 | 콩팥실질의 병변으로 인해 야기된 고혈압. 콩팥의 대표적 기능은 노폐물 및 수분의 배설이다. 그런데 이러한 콩팥기능에 이상이 생겼을 경우 체내에 과잉수분의 축적이 발생하게 된다. 이와같은 과잉수분의 축적은 혈관내 정수압을 상승시켜 고혈압을 유발하게 된다. 치료는 원인 콩팥병의 교정이며 이유를 모르는 원발고혈압과 달리 콩팥성고혈압의 경우에는 원인 콩팥병이 교정되면 고혈압도 사라지게 된다. |
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| 영문 | renal cell carcinoma | 한글 | 콩팥세포암종 |
|---|---|---|---|
| 설명 | 콩팥에 생긴 원시콩팥조직에서 발생한 암. 주로 원시세뇨관조직에서 발생한다. 대표적인 세포조직형은 염색시 세포질이 맑게 비어보이는 맑은세포암종이다. 치료는 수술과 항암화학요법이며 아주 드물지만 저절로 낫는 경우도 있는 것으로 보고되어 있다. |
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| 영문 | renal transplantation | 한글 | 콩팥이식 |
|---|---|---|---|
| 설명 | 콩팥병을 가지고 있으나 치료가 불가능한 만성콩팥기능상실 등의 질병을 가진 환자의 신장을 떼어내고 환자와 항원성이 유사한 사람의 콩팥을 이식해주는 것. 이 때 서로간의 항원성의 유사점이 많아야 거부반응이 일어나지 않는다. 그리고 일단 콩팥이식을 받은 사람은 오랜기간 동안 면역억제제를 투여하여 거부반응을 줄여야 한다. 대개 이식된 콩팥은 엉덩뼈오목에 위치하게 된다. |
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| 영문 | infectious disease | 한글 | 감염병 |
|---|---|---|---|
| 설명 | 바이러스로부터 기생충 크기까지의 생물을 원인으로 하는 병. 원인은 접촉전염성이며, 병원에서 감염되는 경우도 있다. 감염을 원인균에 따라 분류하면 바이러스, 세균, 클라미디아, 리켓차, 미코박테리움, 곰팡이, 원충, 윤충, 외부기생충 감염으로 나눌 수 있다. |
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| CRD | carbohydrate-recognition domain; chronic renal disease; chronic respiratory disease; child restraint... |
|---|---|
| RD | radial deviation; radiology department; rate difference; Raynaud disease; reaction of degeneration; ... |
| CD | cadaver donor; canine distemper; canine dose; carbohydrate dehydratase; carbon dioxide; cardiac dise... |
| HD | Haab-Dimmer [syndrome]; Hajna-Damon [broth]; Hansen disease; hearing distance; heart disease; helix ... |
| MD | Doctor of Medicine [Lat. Medicinae Doctor]; magnesium deficiency; main duct; maintenance dose; major... |
| APKD | Adult polycystic kidney disease |
|---|---|
| ADPKD | Autosomal Dominant Polycystic Kidney Disease |
| ARPKD | Autosomal recessive polycystic kidney disease |
| PCOD | Polycystic Ovary Disease |
| PKD | Polycystic kidney disease |
Kugelberg-Welander disease 근 위축증의 유전성 연소형으로서 보통 상염색체성 열성 형질로 유전된다. 척수 전각의 병변이 그 원인이다.
kukuruku 원인 불명이며, 나이지리아에서 볼 수 있는 질환으로, 열
| polycystic disease of kidneys | A progressive disease characterised by formation of multiple cysts of varying size scattered diffusely throughout both kidney's, resulting in compression and destruction of kidney parenchyma, usually with hypertension, gross haematuria, and uraemia; there are two major types: 1) with onset in infancy or early childhood, usually with autosomal recessive inheritance; 2) with onset in adulthood, with autosomal dominant inheritance. Synonym: polycystic disease of kidneys. (05 Mar 2000) |
|---|---|
| polycystic kidney disease | <disease> A rare inherited condition in which the kidney are composed of multiple cysts. Kidney cysts are associated with an increased incidence of cerebral aneurysm. Symptoms usually appear later (if they do at all) and include blood in the urine, flank pain, excessive urination at night and abdominal pain. Individuals may also have elevated blood pressure. Chronic (end-stage renal disease) renal failure is the most common result in the 5th to 6th decades of life. Incidence: 1 in 5,000. (02 Jan 1998) |
| polycystic liver disease | Gradual cystic dilation of intralobular bile ducts (Meyenburg's complexes) that fail to involute in embryologic development of the liver; frequently associated with bilateral congenital polycystic kidneys and occasionally with cystic involvement of the pancreas, lungs, and other organs. Synonym: polycystic liver disease. (05 Mar 2000) |
| polycystic ovarian disease | <disease> A condition found among women who do not ovulate, characterised by multiple ovarian cysts and increased androgen production. (09 Oct 1997) |
| disease, ovarian, polycystic | See Disease, polycystic ovarian. (12 Dec 1998) |
| disease, polycystic kidney | Genetic (inherited) disorders characterised by the development of innumerable cysts in the kidneys filled with fluid that replace much of the mass of the kidneys and reduce kidney function leading to kidney failure. (12 Dec 1998) |
| disease, polycystic ovarian | An hormonal problem that causes women to have a variety of symptoms including irregular or no periods, acne, obesity and excessive hair growth. Women with PCO are at a higher risk for uterine cancer (endometrial cancer), diabetes, high blood pressure, and heart disease. With proper treatment, risks can be minimised. PCO is also known as Stein-Leventhal syndrome. (12 Dec 1998) |
| polycystic | Composed of many cysts. (05 Mar 2000) |
| polycystic kidney | A progressive disease characterised by formation of multiple cysts of varying size scattered diffusely throughout both kidney's, resulting in compression and destruction of kidney parenchyma, usually with hypertension, gross haematuria, and uraemia; there are two major types: 1) with onset in infancy or early childhood, usually with autosomal recessive inheritance; 2) with onset in adulthood, with autosomal dominant inheritance. Synonym: polycystic disease of kidneys. (05 Mar 2000) |
| polycystic liver | Gradual cystic dilation of intralobular bile ducts (Meyenburg's complexes) that fail to involute in embryologic development of the liver; frequently associated with bilateral congenital polycystic kidneys and occasionally with cystic involvement of the pancreas, lungs, and other organs. Synonym: polycystic liver disease. (05 Mar 2000) |
| polycystic ovary | Enlarged cystic ovary's, pearl white in colour, with thickened tunica albuginea, characteristic of the Stein-Leventhal syndrome; clinical features are abnormal menses, obesity, and evidence of masculinization, such as hirsutism. (05 Mar 2000) |
| polycystic ovary syndrome | <syndrome> Clinical symptom complex characterised by oligomenorrhoea or amenorrhoea, anovulation, and regularly associated with bilateral polycystic ovaries. (12 Dec 1998) |
| kidney, polycystic | Kidney whose tissue is displaced by a large number of tightly packed cysts so that cystic volume predominates over the solid parts to a considerable degree. (12 Dec 1998) |
| kidney, polycystic, autosomal dominant | A genetic disorder with autosomal dominant inheritance characterised by multiple cysts in both kidneys and progressive deterioration of renal function. It is usually caused by a mutant gene at the pkd1 locus on the short arm of chromosome 16, though mutations elsewhere in the genome can also cause the disease. The age of onset of symptoms varies widely. (12 Dec 1998) |
| kidney, polycystic, autosomal recessive | Rare genetic disorder with autosomal recessive inheritance characterised by multiple cysts in both kidneys and associated hepatic lesions. Serious manifestations are usually present at birth and there is high perinatal mortality. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|