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| AM | Academic Medicine [journal]; actomyosin; acute myelofibrosis; adult male; adult monocyte; aerospace ... |
|---|---|
| AFP | Alpha(¥á) Feto-Protein [HP 1826, 1858, 1859, 2265] ; Oncofetal Antigens &nbs... |
| MT | magnetization transfer; malaria therapy; malignant teratoma; mammary tumor; mammilothalamic tract; m... |
| MTA | malignant teratoma, anaplastic; medical technical assistant; medical technology assessment; metatars... |
| MTI | malignant teratoma, intermediate; minimum time interval; moving target indicator |
| AAI | Adult Attachment Interview |
|---|---|
| ABLES | Adult Blood Lead Epidemiology and Surveillance program |
| ACOA | Adult Children Of Alcoholics |
| ADHC | Adult Day Health Care |
| ADRV | Adult Diarrhoea Rotavirus |
| malignant teratoma | <oncology, tumour> A collection of cancerous cells which form cysts that contain one or more of the three primary embryonic germ layers: skin, hair or teeth. (27 Sep 1997) |
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| sacrococcygeal teratoma | <tumour> Found in the region of the primitive pit and node. Most common tumour in the newborn period. Triphyllomatous teratoma, a teratoma composed of tissues derived from all three germ layers. Synonym: tridermoma. (05 Mar 2000) |
| ovarian teratoma | See: Ovary, dermoid cyst of the. (12 Dec 1998) |
| teratoma | <oncology, tumour> Malignant tumour (teratoma) thought to originate from primordial germ cells or misplaced blastomeres that contains tissues derived from all three embryonic layers, such as bone, muscle, cartilage, nerve, tooth buds and various glands. Accompanied by undifferentiated, pluripotent epithelial cells known as embryonal carcinoma cells. (16 Dec 1997) |
| teratoma orbitae | Unequal conjoined twins in which the parasite, usually very imperfectly developed, is attached at an orbit of the autosite. See: conjoined twins. Synonym: teratoma orbitae. Origin: L. Orbita, orbit, + G. Pagos, something fixed (05 Mar 2000) |
| teratoma, ovarian | Tumour that develops from a totipotential germ cell (a primary oocyte) retained within the egg sac (ovary). Being totipotential, that cell can give rise to all orders of cells necessary to form mature tissues and often recognizable structures such as hair, bone and sebaceous (oily) material, neural tissue and teeth. These tumours may occur at any age but the prime age of detection is in the childbearing years. The average age is 30. Up to 15% of women with ovarian teratomas have them in both ovaries. The tumours can range in size from a centimeter (less than a half inch) up to 45 cm (17 inches) in diameter. They can cause the ovary to twist (torsion) and imperil its blood supply. Although the large majority (about 98%) of ovarian teratomas are benign, the remaining fraction (about 2%) becomes malignant. The larger the ovarian teratoma, the greater the risk of rupture with spillage of the greasy contents which can create problems with adhesions, pain etc. Removal is usually the treatment of choice by laparotomy (surgery) or laparoscopy (with a scope). Ovarian teratomas are also called dermoid cysts of the ovary and referred to simply as dermoids. (12 Dec 1998) |
| adult | A living organism which has attained full growth or maturity. Origin: L. Adultus = grown up (18 Nov 1997) |
| adult lactase deficiency | Onset of lactase deficiency, with resulting milk intolerance and malabsorption, in adulthood. Inherited forms may not be manifested until adulthood; any process that damages the intestinal lining cells can cause lactase deficiency in adults. (05 Mar 2000) |
| adult medulloepithelioma | <tumour> Malignant hyperplasia of ciliary epithelium with frequent involvement of the pigmented layer. Synonym: adult medulloepithelioma. (05 Mar 2000) |
| adult-onset diabetes | <disease> An often mild form of diabetes mellitus of gradual onset, usually in obese individuals over age 35; absolute plasma insulin levels are normal to high, but relatively low in relation to plasma glucose levels; ketoacidosis is rare, but hyperosmolar coma can occur; responds well to dietary regulation and/or oral hypoglycaemic agents, but diabetic complications and degenerative changes can develop. (05 Mar 2000) |
| adult-onset still's disease | Although Still's disease was first described in children, it is known to begin in adults. See: Still's disease. (12 Dec 1998) |
| adult pseudohypertrophic muscular dystrophy | Muscular dystrophy of late onset, often in the second or third decade, with relatively mild course; X-linked recessive inheritance; perhaps allelic with Duchenne's dystrophy, but milder and not a genetic lethal. Compare: Duchenne dystrophy. Synonym: Becker type tardive muscular dystrophy. (05 Mar 2000) |
| adult respiratory distress syndrome | <chest medicine, syndrome> A clinical syndrome that includes pulmonary insufficiency. It is a descriptive term that is applied to a variety of diffuse infiltrative processes in the lung. Manifestations include severe shortness of breath, rapid breathing and arterial hypoxaemia (low oxygen). Chest X-ray shows bilateral diffuse infiltrates. Treatment most often includes mechanical respiratory support. Causes include toxic gas (chlorine, NO2, smoke) exposure, severe metabolic derangement, gastric acid aspiration, pancreatitis, sepsis and trauma. Acronym: ARDS (12 Jul 2000) |
| adult rickets | <pathology> A condition marked by softening of the bones (due to impaired mineralisation, with excess accumulation of osteoid), with pain, tenderness, muscular weakness, anorexia and loss of weight, resulting from deficiency of vitamin D and calcium. Origin: Gr. Malakia = softness (18 Nov 1997) |
| adult T-cell leukaemia | Lymph nodes show a mixture of small and large atypical cells which are polymorphic and express nuclear pleiomorphism. Adult T-cell leukaemia is caused by HTLV-1 and is rare in the US and Europe but common in Japan. Tumour cells express CD2, CD3, CD5 and lack CD7. The most common chromosome change reported in adult T-cell leukaemia is presence of the 14q + marker (05 Mar 2000) |
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