| 영문 | hyperplasia | 한글 | 과다형성, 증식 |
|---|---|---|---|
| 설명 | 기능항진을 유발시키는 자극을 받았을 때 분열이 가능한 세포가 세포분열로 그 수가 증가되는 것을 증식이라 하며, 결과적으로 그 조직이나 장기도 커지게 된다. 비대는 단순히 세포의 증식이 없이 세포의 크기가 커지는 경우를 이르는 말이다. |
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| 영문 | adrenal gland | 한글 | 부신 |
|---|---|---|---|
| 설명 | 콩팥위에 존재하는 피라밋모양의 구조물. 겉질과 속질로 되어 있으며 호르몬의 분비가 주역할이다.  |
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| 영문 | adrenal medulla | 한글 | 부신속질 |
|---|---|---|---|
| 설명 | 부신의 안쪽에 있는 부분으로 부교감신경의 지배를 받아서 카테콜라민(catecholamine)을 분비한다. |
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| 영문 | Benign Prostatic Hyperplasia(BPH) | 한글 | 전립샘비대 |
|---|---|---|---|
| 설명 | 50세 이상의 남성에 빈발하는 병으로 전립샘의 요도 주위 영역에 큰결절을 형성하여, 이것이 커지면 요도를 압박하여 부분적 혹은 완전한 요도폐색을 일으키는 병이다. 증상은 요도폐색에 따른 소변의 감소와 방광자극증상으로 빈뇨, 잔뇨감, 소변을 참을 수 없는 증상 등이다. 치료는 경요도 전립샘 적출술로 전립선의 비대한 부분을 절제해야 한다. |
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| CLAH | congenital lipoid adrenal hyperplasia |
|---|---|
| CAH | 1) Chronic Active Hepatitis 2) Congenital Adrenal Hyperplasia |
| CAH | chronic active hepatitis; chronic aggressive hepatitis; combined atrial hypertrophy; congenital adre... |
| CVAH | congenital virilizing adrenal hyperplasia |
| IAH | idiopathic adrenal hyperplasia; implantable artificial heart |
| lipoid CAH | lipoid adrenal hyperplasia |
|---|---|
| CAH | Cogenital adrenal hyperplasia |
| LN | lipoid nephrosis |
| AA | Adrenal androgen |
| AHC | Adrenal hypoplasia congenita |
| adrenal hyperplasia | <pathology> A condition of diffuse enlargement of the adrenal glands. Origin: Gr. Plassein = to form (27 Sep 1997) |
|---|---|
| adrenal hyperplasia, congenital | A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form. (12 Dec 1998) |
| congenital adrenal hyperplasia | <endocrinology> A genetic disorder present at birth characterised by a deficiency of the hormones aldosterone and cortisol and an overproduction of male sex hormones (androgens). In males this may manifest as enlarged penis, small testes and early development of masculine characteristics. In females features include ambiguous genitalia, failure to menstruate, deep voice and excessive hair. Origin: Gr. Plassein = to form (27 Sep 1997) |
| congenital virilizing adrenal hyperplasia | A series of inherited inborn errors of metabolism with hyperplasia of the adrenal cortex and overproduction of virilizing hormones. Most common forms are due to partial or complete 21-hydroxylase deficiency, leading to increased ACTH production by the pituitary, stimulating adrenal growth and function. Severe form is characterised by salt-losing state. (05 Mar 2000) |
| nephrosis, lipoid | Glomerular disease causing heavy proteinuria characterised by absence of obvious histologic glomerular changes on light microscopy. It is also called minimal change glomerular disease and minimal lesion glomerulonephritis. (12 Dec 1998) |
| lipoid | 1. Resembling fat. 2. Former term for lipid. Synonym: adipoid. Origin: Lipo-+ G. Eidos, appearance (05 Mar 2000) |
| lipoid granuloma | Granuloma characterised by aggregates or accumulations of fairly large mononuclear phagocytes that contain lipid. (05 Mar 2000) |
| lipoid nephrosis | <nephrology> A disorder of the kidneys which largely affects the glomerulus, the blood filtering structure. This disorder is one common cause of nephrotic syndrome in children affecting 2 to 3 children per 100,000 population under age 16 in the us. Minimal change disease is also seen rarely in adults. The cause is unknown but may be related to an autoimmune illness. Risk factors include a history for a immune disorder, recent immunisation or a bee sting. Diagnosis is made by renal biopsy. Treatment include systemic corticosteroids which are usually quite effective in curing this disease. Other medications include chlorambucil and cyclophosphamide. In most cases, a moderate protein diet (1 gram protein per Kg body weight per day) will be recommended. Salt (sodium) restriction can be helpful to reduce swelling and vitamin D is usually supplemented. (27 Sep 1997) |
| lipoid proteinosis | <disease> A familial disease occurring in the course of latent diabetes, marked by yellowish nodules due to deposits of a protein-lipid complex on the oral tongue and sublingual and faucial areas, translucent keratotic papillomatous eyelid lesions, keratotic lesions on the extremities, and hoarseness. It is due to a disturbance of lipid metabolism with autosomal recessive inheritance and is frequently associated with intracranial calcifications. inheritance: autosomal recessive. Synonym: hyalinasis cutis et mucosae, lipoidosis cutis et mucosae, Urbach-Wiethe disease. (05 Mar 2000) |
| lipoid theory of narcosis | That narcotic efficiency parallels the coefficient of partition between oil and water, and that lipoids in the cell and on the cell membrane absorb the drug because of this affinity. Synonym: Meyer-Overton theory of narcosis. (05 Mar 2000) |
| angiofollicular mediastinal lymph node hyperplasia | Solitary masses of lymphoid tissue containing concentric perivascular aggregates of lymphocytes, occurring usually in the mediastinum or hilar region of young adults; similar changes have been reported outside the mediastinum and, if associated with interfollicular sheets of plasma cells, may progress to lymphoma or plasmacytoma. Synonym: angiofollicular mediastinal lymph node hyperplasia, Castleman's disease. (05 Mar 2000) |
| angiolymphoid hyperplasia with eosinophilia | Solitary or multiple benign cutaneous nodules comprised of immature and mature vascular structures intermingled with endothelial cells and a varied infiltrate of eosinophils, histiocytes, lymphocytes, and mast cells. (12 Dec 1998) |
| atypical melanocytic hyperplasia | Proliferation of melanocytes showing nuclear atypicality, especially as scattered single cells high in the epidermis; interpreted by some pathologists as malignant melanoma in situ. (05 Mar 2000) |
| basal cell hyperplasia | Increase in the number of cells in an epithelium resembling the basal cells. (05 Mar 2000) |
| benign giant lymph node hyperplasia | Solitary masses of lymphoid tissue containing concentric perivascular aggregates of lymphocytes, occurring usually in the mediastinum or hilar region of young adults; similar changes have been reported outside the mediastinum and, if associated with interfollicular sheets of plasma cells, may progress to lymphoma or plasmacytoma. Synonym: angiofollicular mediastinal lymph node hyperplasia, Castleman's disease. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|