| 영문 | carcinoma in situ | 한글 | 상피내암종 |
|---|---|---|---|
| 설명 | 신체의 내부나 외부를 쌓고 있는 조직을 상피라고 한다. 이 상피의 아래에는 대개 상피를 지지하고 있는 조직의 위에 존재한다. 그리고 이 지지조직과 상피 사이에는 기저막이라는 막이 있어서 상피와 지지조직을 구분해 준다. 암종(carcinoma)란 상피의 세포가 악성 변화를 하여 생기는 암을 말한다. 제자리암종이란 암종의 한 종류로 암종이 기저막을 벗어나지 못하고 상피내 즉, 제자리에 머물러 있는 경우를 말한다. |
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| 영문 | carcinoma | 한글 | 암종 |
|---|---|---|---|
| 설명 | 암종이란 상피세포(-신체의 내부나 외부를 쌓고 있는 조직을 상피라고 하고, 상피를 이루고 있는 세포를 상피세포라고 한다)의 과도한 증식에의한 악성종양을 이르는 말이다. |
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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 | squamous cell carcinoma | 한글 | 편평세포암종 |
|---|---|---|---|
| 설명 | 편평세포 기원의 암으로서, 편평세포가 있는 어떤 곳에서든 발생가능함. 따라서 식도암, 피부암, 폐암, 자궁암 등이 여기에 해당된다. 특히 피부암은 많은 자외선조사에 의해 생기는 광선각화증에서 발생가능하다. 병리조직학적 특성으로서 각질을 생성한다. |
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| HCG, hCG | Human Chorionic Gonadotropin; 사람융모성성선자극호르몬 1. Placental Glycoprotein Hormone &nbs... |
|---|---|
| HPA axis | Hypothalamic-Pituitary-Adrenal axis |
| AA | abdominal aorta; acetic acid; achievement age; active alcoholic; active assistive [range of motion];... |
| AACSH | adrenal androgen corticotropic stimulating hormone |
| AASH | adrenal androgen stimulating hormone; American Association for the Study of Headache |
| 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) |
| adrenal crisis | <endocrinology> An abrupt life-threatening state which is caused by insufficient production of cortisol by the adrenal gland. A typical finding in Addison's disease. Individuals who have been taking corticosteroids (glucocorticoids) for a prolonged period of time (weeks to months) are at risk for acute adrenal crisis if the medication is stopped abruptly. For this reason, corticosteroid medication are withdrawn slowly on a diminishing dosing schedule. Symptoms include low blood pressure (shock), weakness, headache, vomiting, fever chills, tachycardia and sweating. Treatment includes blood pressure support and intravenous hydrocortisone. (27 Sep 1997) |
| adrenal cyst | <radiology> Same characteristics as renal cysts, but less common, thick wall, septations, calcifications suggests pseudocyst (12 Dec 1998) |
| adrenal gland | <anatomy, endocrinology> This gland is found above each kidney and it made up of an outer wall (cortex) that secretes important steroid hormones and an inner portion (medulla) that produces adrenaline (adrenaline) and noradrenaline (noradrenaline). The hormones help control heart rate, blood pressure, the way the body uses food, and other vital functions. (25 Jun 1999) |
| adrenal gland hypofunction | Adrenocortical hypofunction includes all conditions in which adrenal steroid hormone secretion falls below the requirements of the body. Adrenal insufficiency may be divided into two general categories: (1) those associated with primary inability of the adrenal to elaborate sufficient quantities of hormone and (2) those associated with a secondary failure due to a primary failure in the elaboration of adrenocorticotropin. (12 Dec 1998) |
| adrenal gland insufficiency | <endocrinology> A condition that results from the inadequate production of adrenal hormones (see Addison's disease). (27 Sep 1997) |
| adrenal gland tumour | <oncology> A benign tumour or adenoma, that usually results in the excess production of adrenal gland hormones. (27 Sep 1997) |
| adrenal haemorrhage | <radiology> Neonate, right more common, 10% bilateral, birth trauma, hypoxia, septicaemia, congenital syphilis, haemorrhagic disorders (haemophilia, etc.) adult, septicaemia (Waterhouse-Friderichsen syndrome), tumour, trauma Notes: usually resolves in 4-6 weeks, adrenal insufficiency rare, even if bilateral, may calcify (12 Dec 1998) |
| adrenal hermaphroditism | Altered appearance of the genitalia due to disorders of adrenocortical function, most often female virilization; not an example of true hermaphroditism. (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) |
| adrenal hypertension | Hypertension due to an adrenal medullary pheochromocytoma or to hyperactivity or functioning tumour of the adrenal cortex. (05 Mar 2000) |
| adrenal imaging | <radiology> Cortex, I-131 iodo-cholesterol, not widely used due to high rad dose and 4-15 day delayed imaging, medulla, search for pheo, MIBG (I-131 meta-iodobenzylguanidine) (12 Dec 1998) |
| adrenal insufficiency | <endocrinology> A condition that results from the inadequate production of adrenal hormones (see Addison's disease). (27 Sep 1997) |