| 영문 | nuclear medicine | 한글 | 핵의학 |
|---|---|---|---|
| 설명 | 방사성을 띠는 핵물질을 이용하여 의학에 응용하는 학문. 대개 인체에 큰 해가 없는 방사선물질을 사용하며, 반감기가 짧아 사용후에도 큰 해가 없다. 이런 핵의학적 물질을 이용한 핵의학적 진단의 가장 큰 장점은 생체내에서 일어나는 그 기관의 실제적인 기능을 알아볼 수 있다는 데 있다. 흔히 접하는 X-선을 이용한 진단방법은 단지 그 순간만의 영상을 접하여 실제로 보이는 부위가 얼마나 기능을 수행하는지 알 수 없는 단점이 있으나, 핵의학에서는 실제적인 기능의 정도에 따라 영상이 나오게 되므로 기능판별에 아주 유리하다. 하지만, 정확한 판별력이 있는 영상을 얻기에는 부족하다. 또한 핵의학은 진단외의 치료에도 사용되는데, 예를 들어 갑상샘종양의 경우 여러 곳에 이미 전이가 되어 있을 경우 방사선핵종을 이용하여 다른 곳에 큰 부작용없이 치료가 가능하다. |
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| 영문 | nuclear magnetic resonance(NMR) | 한글 | 핵자기공명 |
|---|---|---|---|
| 설명 | 다른 말로 MRI=Magnetic Resonance Imaging 자기공명영상이라고도 한다. 인체의 장기나, 병적인 모양, 종양의 위치, 림프절의 비대 등에 대한 진단을 내리기 위해 시행하는 방사선학적인 검사방법이다. 현재 많이 쓰이고 있는 컴퓨터단층촬영(CT=computerized tomography)과는 다른 방법으로 시행하며, 그 해상도가 컴퓨터단층촬영보다는 뛰어나 비록 고가이긴 하지만, 많이 쓰이고 있다. 또한 인체에 무해하고, 여러 가지 면(plane)에서 사람을 단층시켜 볼 수 있다. 단점은 심장박동기를 설치한 사람이나, 주위에 자장을 띠는 물체를 몸에 지니고 있는 중환자 등에서는 이용할 수 없고, 복부장기에 대한 진단에는 컴퓨터단층촬영보다 떨어지는 것으로 되어 있다. |
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| MURCS Associations | MUllerian duct aplasia, Renal aplasia, Cervico-thoracic vertebral(Somite) dysplasia Associations |
|---|---|
| NM | near-miss; neomycin; neuromedin; neuromuscular; neutrophil migration; nictitating membrane; nitrogen... |
| PRCA | Pure Red Cell Aplasia |
| ACC | accommodation; acetyl coenzyme A carboxylase; acinic cell carcinoma; acute care center; adenoid cyst... |
| ARCA | acquired red cell aplasia |
| ACC | Aplasia cutis congenita |
|---|---|
| PRCA | Pure Red Cell Aplasia |
| nuclear VV | nuclear volume |
| (1)H-NMR | 1)H-nuclear magnetic resonance |
| NMR | 1)H-nuclear magnetic resonance |
| aplasia | <embryology> A lack of development of an organ or tissue or of the cellular products from an organ or tissue. Compare: hypoplasia. Origin: Gr. Plassein = to form (18 Nov 1997) |
|---|---|
| aplasia cutis congenita | Congenital absence or deficiency of a localised area of skin, with the base of the defect covered by a thin translucent membrane; most often a single area near the vertex of the scalp, but may occur in other areas; underlying structures may also be affected; autosomal inheritance, either dominant or recessive. (05 Mar 2000) |
| radial aplasia-thrombocytopenia syndrome | <syndrome> Aplasia (absence) of the radius (the long bone on the thumb-side of the forearm) and thrombocytopenia (low blood platelets) are key features characterizing this syndrome. There is phocomelia (flipper-limb) with the thumbs always present. The fibula (the smaller bone in the lower leg) is often absent. The risk of bleeding from too few platelets is high in early infancy but lessens with age. The condition is inherited in an autosomal recessive trait with one gene (on a non-sex chromosome) coming from each parent to the child affected with the disease. Alternative names include thrombocytopenia-absent radius syndrome, tar syndrome, and tetraphocomelia-thrombocytopenia syndrome. (12 Dec 1998) |
| germinal aplasia | A disorder in which the seminiferous tubules exhibit an abnormal cytoarchitecture and extensive hyalinization; the testes are small, and few spermatozoa are formed; the body habitus may be eunuchoid, and gynaecomastia may be present; urinary gonadotropin output is usually high, and the incidence of mental deficiency and illness increased; sex chromatin may be male or female, and androgen secretion ranges from subnormal to normal. It is a constant feature of (and is often used synonymously with) Klinefelter's syndrome. Synonym: germinal aplasia. (05 Mar 2000) |
| red-cell aplasia, pure | Suppression of erythropoiesis with little or no abnormality of leukocyte or platelet production. (12 Dec 1998) |
| gonadal aplasia | Congenital absence of essentially all gonadal tissue; the external genitalia and genital ducts are female, but if interstitial cells of Leydig are present, the external genitalia are commonly ambiguous and the genital ducts are female. See: gonadal dysgenesis. Compare: Klinefelter's syndrome, Turner's syndrome. Synonym: gonadal agenesis. (05 Mar 2000) |
| congenital aplasia of thymus | diGeorge syndrome |
| pure red cell aplasia | A transitory arrest of red blood cell production which may occur in the course of a haemolytic anaemia, often preceded by infection, or as a complication of certain drugs; if the arrest persists anaemia may result. See: congenital hypoplastic anaemia. (05 Mar 2000) |
| syndrome, radial aplasia-thrombocytopenia | See syndrome, tar. (12 Dec 1998) |
| thymic aplasia | <disease, immunology> A lack of T lymphocytes, due to failure of the thymus to develop, resulting in very reduced cell-mediated immunity though serum immunoglobulin levels may be normal. See: DiGeorge syndrome. Origin: Gr. Plassein = to form (18 Nov 1997) |
| receptors, cytoplasmic and nuclear | Proteins in the cytoplasm or nucleus that specifically bind signalling molecules and trigger changes which influence the behaviour of cells. The major groups are the steroid hormone receptors, which usually are found in the cytoplasm, and the thyroid hormone receptors, which usually are found in the nucleus. Receptors, unlike enzymes, generally do not catalyze chemical changes in their ligands. (12 Dec 1998) |
| Remak's nuclear division | <cell biology> An unusual form of nuclear division, in which the nucleus simply constricts, rather like a cell without chromosome condensation or spindle formation. Partitioning of daughter chromosomes is haphazard. Observed in some Protozoa. (18 Nov 1997) |
| Pelger-Huet nuclear anomaly | Congenital inhibition of lobulation in the nuclei of neutrophilic leukocytes; most cells present band or bilobulate appearance, and only an occasional cell is trilobed; it is not associated with disease, but may be confused with leukocyte "shift to left"; autosomal dominant inheritance. (05 Mar 2000) |
| ribonucleoproteins, small nuclear | Highly conserved nuclear RNA-protein complexes that function in RNA processing in the nucleus, including pre-mRNA splicing and pre-mRNA 3'-end processing in the nucleoplasm. The u3 snrnp is localised in the nucleolus, where it aligns into base pairs with the 28s rrna precursor in a still unidentified region and functions in pre-rrna processing. The u7 snrnp aligns into base pairs with a conserved sequence in the 3'-end of histone pre-mRNA and is an essential cofactor for the cleavage that creates the mature nonadenylated 3'-end. (12 Dec 1998) |
| RNA, heterogeneous nuclear | Nuclear nonribosomal RNA larger than about 1000 nucleotides, the mass of which is rapidly synthesised and degraded within the cell nucleus. Some heterogeneous nuclear RNA may be a precursor to mRNA. However, the great bulk of total hnrna hybridises with nuclear DNA rather than with mRNA. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|