| 영문 | endocrine gland | 한글 | 내분비샘 |
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| 설명 | 신체의 내부로 분비가 되어서 다른 세포의 기능이나 활성의 변화를 일으키는 물질인 호르몬을 분비하는 곳을 이르는 말이다. 대표적인 내분비샘은 갑상샘, 부갑상샘, 부신, 이자, 뇌하수체, 난소, 고환, 솔방울샘, 가슴샘 등이다. 마지막에 나오는 2개의 기관은 내분비 기능을 하는 것으로 생각이 되지만 확실히 그것이 무슨 기능을 하는 지에 대해선 아직까지 정확하게 밝혀지지 않고 있다.  |
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| MEN | Multiple Endocrine Neoplasia ; AD Trait 1. MEN Type I(= Wermer Syndro... |
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| EC | effective concentration; ejection click; electrochemical; electron capture; embryonal carcinoma; eme... |
| SEGNE | secretory granules of neural and endocrine [cells] |
| GUT | Genito-Urinary Tract |
| GA | Gamblers Anonymous; gastric analysis; gastric antrum; general anesthesia; general angiography; gener... |
| gut GLI | Gut glucagon-like immunoreactivity |
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| GALT | Gut associated lymphoid tissue |
| GKLF | Gut-enriched Kruppel-like factor |
| WGTT | Whole gut transit time |
| GALT | gut associated lymphoreticular tissues |
| endocrine cells of gut | Cells found throughout the lining of the gastrointestinal tract that contain regulatory peptide hormones and/or biogenic amines. The substances are located in secretory granules and act in an endocrine or paracrine manner. Some of these substances are also found in neurons in the gut. There are at least 15 different types of endocrine cells of the gut. Some take up amine precursors and have been called apud cells. However, most endocrine cells of the gut apparently have endodermal rather than neuroectodermal origin, so the relationship with apud cells is not clear. (12 Dec 1998) |
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| blind gut | <anatomy> A blind pouch-like commencement of the colon in the right lower quadrant of the abdomen at the end of the small intestine. The appendix is a diverticulum that extends off the caecum. (13 Nov 1997) |
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| gut | 1. A narrow passage of water; as, the Gut of Canso. 2. An intenstine; a bowel; the whole alimentary canal; the enteron; (pl) bowels; entrails. 3. One of the prepared entrails of an animal, especially. Of a sheep, used for various purposes. See Catgut. 4. The sac of silk taken from a silkworm (when ready to spin its cocoon), for the purpose of drawing it out into a thread. This, when dry, is exceedingly strong, and is used as the snood of a fish line. Blind gut. See Caecum, . Origin: OE. Gut, got, AS. Gut, prob. Orig, a channel, and akin to geotan to pour. See FOUND to cast. Source: Websters Dictionary (01 Mar 1998) |
| gut-associated lymphoid tissue | <physiology> Peripheral lymphoid organ consisting of lymphoid tissue associated with the gut (Peyer's patches, tonsils, mesenteric lymph nodes and the appendix). It is especially rich in B-cells and is responsible for localised immunity to pathogens such as bacteria, viruses, and parasites. (20 Sep 2002) |
| postanal gut | An extension of the hindgut caudal to the point at which the anal opening is formed. Synonym: postcloacal gut, tailgut. (05 Mar 2000) |
| postcloacal gut | An extension of the hindgut caudal to the point at which the anal opening is formed. Synonym: postcloacal gut, tailgut. (05 Mar 2000) |
| preoral gut | The part of the embryonic foregut extending cephalad to the level of the oral plate and caudal to the pituitary diverticulum (Rathke's pouch). Synonym: preoral gut. (05 Mar 2000) |
| primitive gut | A flat sheet of intraembryonic endoderm that will change into a tubular gut due to the folding of embryonic body-head, tail and lateral body folds. Synonym: archenteron, celenteron, endodermal canal, subgerminal cavity. (05 Mar 2000) |
| bone diseases, endocrine | Diseases of the bones related to hyperfunction or hypofunction of the endocrine glands. (12 Dec 1998) |
| multiple endocrine adenomatosis | The presence of functioning tumours in more than one endocrine gland, commonly the pancreatic islets and parathyroid glands, which may be associated with Zollinger-Ellison syndrome; dominant inheritance. Synonym: multiple endocrine adenomatosis. (05 Mar 2000) |
| multiple endocrine deficiency syndrome | <syndrome> Acquired deficiency of the function of several endocrine glands, usually on an auto-immune basis. Synonym: multiple glandular deficiency syndrome. (05 Mar 2000) |
| multiple endocrine neoplasia | (type I) This is a hereditary disorder in which two or more of the following glands: parathyroid, pancreas, pituitary, adrenals or thyroid develop hyperplasia or a tumour. (type II) This is a hereditary disorder in which two or more of the following glands: thyroid, adrenal or parathyroid, develop overgrowth (hyperplasia) or malignant cells (cancer). The underlying cause is genetic and a positive family history for this illness is a risk factor. Incidence: approximately 3 in 100,000 people in the general population. Origin: Gr. Plassein = to form (27 Sep 1997) |
| multiple endocrine neoplasia 1 | <radiology> Multiple endrocrine neoplasia syndrome three P's. Pituitary adenoma, 65% can develop Cushing's, acromegaly, prolactinoma, parathyroid hyperplasia / adenoma, 88% can develop hyper-PTH pancreatic isleT-cell tumour, gastrinoma (Z-E) most common, 50% of Z-E can develop MEN-1, inconstant features: bronchial/intestinal carcinoid, thyroid adenoma, adrenal cortical tumour, lipoma, thymoma tissue expression Primary hyperparathyroidism (90%), Gastrinoma (30%), Prolactinoma (15%), Other (10%). Synonym: Wermer syndrome (12 Dec 1998) |
| multiple endocrine neoplasia 2 | <radiology> Multiple endocrine neoplasia syndrome, medullary thyroid carcinoma, usually multifocal; metastasis to local nodes, lung, liver, usually calcify in liver, pheochromocytoma, almost always bilateral, parathyroid hyperplasia, may be secondary to calcitonin secreted by medullary thyroid carcinoma inconstant feature: adrenal cortical hyperplasia Synonym: Sipple syndrome (12 Dec 1998) |
| multiple endocrine neoplasia 3 | <radiology> Multiple endocrine neoplasia syndrome (type 2B, type 3), medullary thyroid carcinoma, pheochromocytoma, marfanoid habitus (Cf: Marfan syndrome), mucosal neuromas, neurofibromas, ganglioneuromatosis coli More info: MEN syndrome 2B Synonym: Schimke, marfanoid syndrome (12 Dec 1998) |
| multiple endocrine neoplasia type 1 | A rare syndrome characterised by hyperplasia and/or neoplasms of the pituitary, parathyroid glands, and pancreatic islets. Hyperparathyroidism occurs in 90% of the cases and is usually the first manifestation of the syndrome. The most frequent pancreatic manifestation is gastrinoma typically leading to zollinger-ellison syndrome. The appearance of this condition has been limited to the loss of allelic heterozygosity at the 11q13 locus on the long arm of chromosome 11. Patients overall exhibit long survival times. Chemotherapy is rare and surgical management is generally dependent on the genetic expression in individual patients. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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