| 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. |
||
| 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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| MEN | Multiple Endocrine Neoplasia ; AD Trait 1. MEN Type I(= Wermer Syndro... |
|---|---|
| FH | facial hemihyperplasia; familial hypercholesterolemia; family history; fasting hyperbilirubinemia; f... |
| ACC | accommodation; acetyl coenzyme A carboxylase; acinic cell carcinoma; acute care center; adenoid cyst... |
| ACE | acetonitrile; acetylcholine esterase; acute cerebral encephalopathy; acute coronary event; adrenocor... |
| ACH | acetylcholine; achalasia; active chronic hepatitis; adrenocortical hormone; amyotrophic cerebellar h... |
| ACC | Adrenocortical carcinoma |
|---|---|
| H-P-A | Hypothalamic-pituitary-adrenocortical |
| HPA | Hypothalamo-pituitary-adrenocortical |
| PPNAD | Primary pigmented nodular adrenocortical disease |
| BAC | bovine adrenocortical |
| acute adrenocortical insufficiency | Severe adrenocortical insufficiency when an intercurrent illness or trauma causes an increased demand for adrenocortical hormones in a patient with adrenal insufficiency due to disease or use of relatively large amounts of similar hormones as therapy; characterised by nausea, vomiting, hypotension, and frequently hyperthemia, hyponatraemia, hyperkalaemia, and hypoglycaemia; can be fatal if untreated. Synonym: addisonian crisis, adrenal crisis, Bernard-Sergent syndrome. (05 Mar 2000) |
|---|---|
| adrenocortical | Pertaining to suprarenal cortex. (05 Mar 2000) |
| adrenocortical adenoma | <tumour> A benign tumour of adrenal cortical cells; small unencapuslated nodules of adrenal cortex are probably localised areas of hyperplasia rather than adenoma's; true adenoma's are rare and may be symptomless or associated with Cushing's syndrome or primary aldosteronism. (05 Mar 2000) |
| adrenocortical hormones | Hormone's secreted by the human adrenal cortex; e.g., cortisol, aldosterone, corticosterone. (05 Mar 2000) |
| adrenocortical insufficiency | Loss, to varying degrees, of adrenocortical function. Synonym: hypocorticoidism. (05 Mar 2000) |
| partial adrenocortical insufficiency | Normal basal adrenocortical function with failure of adrenocortical reserve to respond to ACTH stimulation. (05 Mar 2000) |
| chronic adrenocortical insufficiency | Adrenocortical insufficiency usually as the result of idiopathic atrophy or destruction of both adrenal glands by tuberculosis, an autoimmune process, or other diseases; characterised by fatigue, decreased blood pressure, weight loss, increased melanin pigmentation of the skin and mucous membranes, anorexia, and nausea or vomiting; without appropriate replacement therapy, it can progress to acute adrenocortical insufficiency. Synonym: Addison's disease, addisonian syndrome, hyposupradrenalism, morbus Addisonii. (05 Mar 2000) |
| primary adrenocortical insufficiency | Adrenocortical insufficiency caused by disease, destruction, or surgical removal of the adrenal cortices. (05 Mar 2000) |
| secondary adrenocortical insufficiency | Adrenocortical insufficiency caused by failure of ACTH secretion resulting from anterior pituitary disease or inhibition of ACTH production resulting from exogenous steroid therapy. (05 Mar 2000) |
| latent adrenocortical insufficiency | Adrenocortical insufficiency not clinically evident but which can become severe if a sudden stress, such as an intercurrent acute illness, develops. (05 Mar 2000) |
| 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) |
| 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) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|