| 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... |
| MAC | Microcystic adnexal carcinoma |
|---|---|
| RCBF | Renal cortical blood flow |
| ARCD | Acquired renal cystic disease |
| CRD | Chronic renal disease |
| ESRD | End Stage Renal DIsease |
cortical evoked potential (피질 유발 전위
| microcystic 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) |
|---|---|
| renal cortical adenoma | <tumour> One of the usually small adenoma's sometimes found in the renal cortex and derived from renal tubular tissue. (05 Mar 2000) |
| renal cortical lobule | One of the subdivisions of the kidney, consisting of a medullary ray and that portion of the convoluted port (renal corpuscles and convoluted tubules) associated with its collecting duct. Synonym: lobulus corticalis renalis, renal cortical lobule, renculus, reniculus, renunculus. (05 Mar 2000) |
| microcystic adenoma of pancreas | <radiology> Benign tumour of pancreas, M:F = 1:4, peak age 69 years of age, tiny cysts filled with GLYCOGEN, not mucin, large (ca. 10 cm), innumerable small cysts (1mm - 20mm), central stellate scar with or without calcification, hypervascular, head = body = tail, ** associated with von Hippel-Lindau syndrome, Cf: macrocystic adenoma, alias mucinous cystic neoplasm (12 Dec 1998) |
| microcystic epithelial dystrophy | Bilateral, symmetrical intraepithelial cysts in the central area of the cornea of healthy women, without hereditary predisposition. (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) |
| end-stage renal disease | <nephrology> A patient with inadequate renal function to support life. Individuals with end-stage disease must rely in kidney dialysis or peritoneal dialysis to survive. End-stage renal disease may be caused by a number of problems including diabetes, sickle cell disease, hypertension and congenital renal disease (polycystic kidney disease). (27 Sep 1997) |
| adenoma, adrenal cortical | A benign neoplasm of adrenal cortical cells resembling normal adrenal cells histologically but possessing functional autonomy. In general it does not exceed 5 cm in its largest dimension, although benign tumours exceeding 20 cm have been reported. Adrenal cortical adenomas produce hypercortisolism and hyperaldosteronism, but seldom produce adrenogenital syndromes. For the most part the prognosis after surgery is reasonably favourable. (12 Dec 1998) |
| adrenal cortical carcinomas | Large invasive and metastasizing tumours which may cause virilism or Cushing's syndrome. (05 Mar 2000) |
| adrenal cortical syndrome | <syndrome> An inexact (and obsolete) term that has been applied to Cushing's syndrome, Addison's disease, or the adrenogenital syndrome. (05 Mar 2000) |
| blindness, cortical | Total loss of vision in all or part of the visual field due to a lesion in the striate area, characterised by the patient's subjective unawareness of his disability and the absence of cortical functions of vision, with the subcortical functions intact. (12 Dec 1998) |
| carcinoma, adrenal cortical | A malignant neoplasm of adrenal cortical cells demonstrating partial or complete histological and functional differentiation. They are rare, comprising between only 0.05% and 0.2% of all cancers. Women develop functional adrenal cortical carcinomas more commonly than men, but men develop nonfunctioning ones more often than women. Hypercortisolism is the most common presentation for this cancer. Virilism and cushing's syndrome may also result. (12 Dec 1998) |
| generalised cortical hyperostosis | <syndrome> An inherited skeletal dysplasia, with mandibular enlargement and thickening of the diaphyses and calvaria, and increased serum alkaline phosphatase; autosomal recessive inheritance. Synonym: generalised cortical hyperostosis. (05 Mar 2000) |
| metaphysial fibrous cortical defect | A small (less than 2 to 3 cm in diameter) fibrous cortical d. (05 Mar 2000) |
| cortical | <anatomy> Pertaining to or of the nature of a cortex or bark. Origin: L. Corticalis (18 Nov 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|