| ¿µ¹® | thyroid gland | ÇÑ±Û | °©»ó»ù |
|---|---|---|---|
| ¼³¸í | »ç¶÷ÀÇ ¸ö¿¡¼ °¡Àå Å« ³»ºÐºñ»ùÀ¸·Î ¸ñÀÇ ¾ÕÂÊ, ¾Æ·¡ÂÊ¿¡ À§Ä¡Çϰí ÀÖÀ¸¸ç 2¿±À¸·Î ±¸¼ºµÇ¾î ÀÖ´Ù. °¢ ¿±Àº ±â°üÀÇ ¾çÂÊ¿¡ ÀÖÀ¸¸ç Á¼Àº Àß·è¿¡ ÀÇÇØ ¾Õ¿¡¼ ¿¬°áµÇ¾î ÀÖ´Ù. °©»ó»ùÈ£¸£¸óÀΠƼ·Ï½Å(thyroxine)À» ºÐºñÇϰí ÀúÀåÇϸç, Çʿ信 µû¶ó ¹æÃâÇÑ´Ù. ¶ÇÇÑ °©»ó»ùÀº Ƽ·ÎÄ®½ÃÅä´Ñ(thyrocalcitonin)µµ ºÐºñÇÑ´Ù. º´ÀûÀÎ »óÅ¿¡¼ Å©±â°¡ ´ë°³ Áõ°¡Çϰí, ÀϺο¡¼´Â µµ¸®¾î À§ÃàµÇ¸ç, ÅëÁõÀ» ³ªÅ¸³»±âµµ ÇÑ´Ù. |
||
| ¿µ¹® | gland | ÇÑ±Û | »ù |
|---|---|---|---|
| ¼³¸í | ÀÚ½ÅÀÇ ´ë»ó¿¡ Çʿ䰡 ¾ø´Â ¹°ÁúÀ» ¸¸µé¾î ºÐºñÇÏ´Â ¼¼Æ÷°¡ ¸ð¿©¼ ¸¸µå´Â ±¸Á¶. Áï ºÐºñ¹°À» Á¦Á¶ÇÏ´Â ¼¼Æ÷°¡ ¸ðÀÎ °ÍÀÌ´Ù. ¼±¿¡´Â ³»ºÐºñ»ù°ú ¿ÜºÐºñ»ùÀÇ 2°¡Áö°¡ ÀÖ´Ù. ³»ºÐºñ»ùÀ̶õ ¸ö¹ÛÀÌ ¾Æ´Ñ ³»ºÎ, Áï Á÷Á¢ Ç÷ÁßÀ¸·Î ºÐºñ¹°À» ºÐºñÇÏ´Â »ùÀ¸·Î ÀÌ ¶§¿¡ ºÐºñµÇ´Â ¹°ÁúÀ» È£¸£¸óÀ̶ó°í ÇÑ´Ù. À̰ÍÀº ÁÖ·Î ¸ö¾ÈÀÇ ´Ù¸¥ ¼¼Æ÷¿¡ ÀÛ¿ëÀ» ÇÏ¿© ±× ¼¼Æ÷ÀÇ ´ë»ç, ºÐ¿ µîÀÇ º¯È¸¦ ÃÊ·¡ÇÏ°í ¸öÀÇ È¯°æÀÇ º¯È¿¡ µû¸¥ ÀûÀÀÀ» µ½´Â ¿ªÇÒÀ» ÇÑ´Ù. ¿ÜºÐºñ»ùÀ̶õ ¸ö¹ÛÀ¸·Î °ü±¸Á¶¸¦ ÅëÇÏ¿© ºÐºñ¹°À» ³»º¸³»´Â »ùÀ» ¸»ÇÑ´Ù. |
||
| ¿µ¹® | pineal gland | ÇÑ±Û | ¼Ö¹æ¿ï»ù, ¼Û°ú¼± |
|---|---|---|---|
| ¼³¸í | ³úÀÇ Áß¾Ó¼±ºÎÀ§ÀÇ µîÂÊ¿¡ Á¸ÀçÇÏ´Â ³»ºÐºñ±â°üÀÌ´Ù. ¼Ö¹æ¿ï»ùÀº melatoninÀ» ºÐºñÇÑ´Ù. µ¿¹°¿¡¼´Â ¼ººÐȹߴ޿¡ ±â¿©ÇÏ´Â °ÍÀ¸·Î µÇ¾î ÀÖÀ¸³ª, »ç¶÷¿¡¼´Â ±× ±â´ÉÀÌ ¾ÆÁ÷ ¸íȮġ ¾Ê´Ù. |
||
| MEN | Multiple Endocrine Neoplasia ; AD Trait 1. MEN Type I(= Wermer Syndro... |
|---|---|
| HCG, hCG | Human Chorionic Gonadotropin; »ç¶÷À¶¸ð¼º¼º¼±ÀÚ±ØÈ£¸£¸ó 1. Placental Glycoprotein Hormone &nbs... |
| ACC | accommodation; acetyl coenzyme A carboxylase; acinic cell carcinoma; acute care center; adenoid cyst... |
| CbCtx | cerebellar cortex |
| CC | calcaneal-cuboid; calcium cyclamate; cardiac catheterization; cardiac contusion; cardiac cycle; card... |
| adrenal androgen-stimulating hormone | A putative pituitary hormone that may be responsible for increased secretion of adrenal androgens at the time of puberty. (05 Mar 2000) |
|---|---|
| adrenal angiography | <radiology> Adrenal arteriography, 3 arteries: superior - inferior phrenic a., middle - aorta, inferior - renal a., difficult to inject all 3; arteriography usually not attempted adrenal venography, venous sampling, may define anatomy, may rupture capsule and ablate function (12 Dec 1998) |
| adrenal apoplexy | Haemorrhage into the adrenal glands or thrombosis of the adrenal veins, followed by acute adrenal insufficiency, occurring in the Waterhouse-Friderichsen syndrome. (05 Mar 2000) |
| adrenal body | See adrenal gland. (12 Dec 1998) |
| adrenal calcification | <radiology> Haemorrhage, cyst, Addison's disease (e.g., TB, histo), neoplasm, pheochromocytoma, adrenal cortical adenoma/carcinoma, adrenal choristoma (myelolipoma), metastatic melanoma, Wolman disease (12 Dec 1998) |
| adrenal capsule | See adrenal gland. (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) |
| 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 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) |
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|