| 영문 | white blood cell(WBC), leukocyte | 한글 | 백혈구 |
|---|---|---|---|
| 설명 | 혈액내에 골수구계세포와 림프계세포, 단핵구계세포를 모두 통틀어 말한다. 백혈구의 증가가 있으면 대개 감염이 있거나, 혹은 탈수현상이 있음을 의미한다. 또한 지나친 백혈구수의 감소는 인체내 면역기능이 떨어져 있음을 의미하며, 다른 질병에 의해 나타나는 이차적인 현상이 아닌지 꼭 진단을 받아보아야 한다. |
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| 영문 | mast cell | 한글 | 비만 세포 |
|---|---|---|---|
| 설명 | 동물의 결합 조직 가운데 널리 분포하는 세포. 결합조직과 점막조직 내에 있는 호염기성 색소로 이염색성(metachromasia)을 나타내는 과립을 가진 방추형의 세포에 작은 둥근 핵을 가진다. 비만세포의 표면에는 IgE에 대한 수용체가 존재하며, 수용체에 결합한 IgE 분자들끼리 다가의 항원에 의해 서로 연결되면 비만세포 과립탈출 반응이 일어나, 히스타민, 세로토닌, 헤파린 등의 화학전달 물질이 방출되어, 즉시형 알레르기 반응 등의 증상을 일으킨다. 피부, 장막, 혈관 주위, 점막 주변에 있다. |
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| 영문 | cell-mediated immunity | 한글 | 세포매개면역 |
|---|---|---|---|
| 설명 | 면역이란 신체를 외부의 물질로부터 보호하는 행위를 말한다. 여기에는 특이적 면역과 비특이적 면역의 두 가지가 있다. 비특이적 면역이라함은 특정한 물질에 관계하는 면역이 아니라 특정 대상이 없이 모든 외부 물체에 작용할 수 있는 면역을 말한다. 여기에는 소변의 흐름, 눈물의 흐름, 피부의 비투과성 등의 기계적인 것도 포함되고 피속에 돌아다니는 세포 중에서 비특이적으로 외부의 물질을 포식하는 세포들(예를 들면 큰포식세포(macrophage)의 활동도 포함이 된다. 세포매개면역이란 특이한 물질을 감지할 수 있는 세포를 생성하게 하여 그것으로 하여금 그 물질을 포식하게 하는 것을 말한다. |
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| JRA | Juvenile Rheumatoid Arthritis; 연소기 류마토이드 관절염 = Juvenile Chronic Arthritis; 연소기 만성 관절... |
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| JD | jejunal diverticulitis; juvenile delinquent; juvenile diabetes |
| MC | mass casualties; mast cell; Master of Surgery [Lat. Magister Chirurgiae]; maximum concentration; Med... |
| JGCT | juvenile granulosa cell tumor; juxtaglomerular cell tumor |
| ACC | accommodation; acetyl coenzyme A carboxylase; acinic cell carcinoma; acute care center; adenoid cyst... |
| JGCT | Juvenile granulosa cell tumor |
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| AR-JP | Autosomal recessive juvenile parkinsonism |
| GJP | Generalized Juvenile Periodontitis |
| IJ | infective juvenile |
| JA | Juvenile Arthritis |
| juvenile cell | A transitional form of myelocyte with nuclear construction that is intermediate between the mature myelocyte (myelocyte C of Sabin) and the two-lobed granular leukocyte. Synonym: juvenile cell. Origin: meta-+ G. Myelos, marrow, + kytos, cell (05 Mar 2000) |
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| arthritis, juvenile rheumatoid | Rheumatoid arthritis of children occurring in three major subtypes defined by the symptoms present during the first six months following onset: systemic-onset (still's disease, juvenile-onset) polyarticular-onset, and pauciarticular-onset. Adult-onset cases of still's disease (still's disease, adult-onset) are also known. Only one subtype of juvenile rheumatoid arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent. (12 Dec 1998) |
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| benign juvenile melanoma | A benign, slightly pigmented or red superficial small skin tumour composed of spindle-shaped, epithelioid, and multinucleated cells that may appear atypical; most common in children, but also appearing in adults. Synonym: benign juvenile melanoma, epithelioid cell nevus, spindle cell nevus. (05 Mar 2000) |
| rheumatoid arthritis, systemic-onset juvenile | Also known as systemic-onset juvenile chronic arthritis. Still's disease presents with systemic (bodywide) illness including high intermittent fever, a salmon-coloured skin rash, swollen lymph glands, enlargement of the liver and spleen, and inflammation of the lungs (pleuritis) and around the heart (pericarditis). The arthritis may not be immediately apparent but it does appear and may persist after the systemic symptoms are gone. (12 Dec 1998) |
| periodontitis, juvenile | Localised periodontitis in teenagers and young adults. The onset is during the circumpubertal period but the diagnosis can be made beyond puberty. Lesions are confined predominantly to the first permanent molars or incisors and the distribution of lesions is usually symmetrical. The gingiva may appear normal. The lesions are highly active immediately following puberty but later destruction may slow or cease spontaneously. The disease is four times more prevalent in females than males and more prevalent in african americans than in other races or ethnic groups. (12 Dec 1998) |
| xanthogranuloma, juvenile | Benign disorder of infants and children characterised by multiple nodules with lipid-laden, non-langerhans-cell histiocytes. (12 Dec 1998) |
| systemic-onset juvenile chronic arthritis | See: Systemic-onset juvenile rheumatoid arthritis (still's disease). (12 Dec 1998) |
| systemic-onset juvenile rheumatoid arthritis | <rheumatology> A form of joint disease, arthritis, that presents with systemic upset. Clinical signs: high intermittent fever, a salmon-coloured skin rash, swollen lymph glands, enlargement of the liver and spleen, and inflammation of the lungs (pleuritis) and around the heart (pericarditis). The arthritis itself may not be immediately apparent but once apparent, it may persist after the systemic symptoms have resolved. Synonym: Still's disease. (03 Jul 1999) |
| juvenile | Pertaining to youth or childhood, young or immature. (18 Nov 1997) |
| juvenile absence epilepsy | A generalised epilepsy syndrome with onset around puberty, characterised by absence seizures and generalised tonic-clonic seizures. EEG often shows a greater than 3 Hz generalised spike wave pattern. (05 Mar 2000) |
| juvenile angiofibroma | <oncology, tumour> A benign tumour of the posterior nasopharynx that is most common in adolescent boys. Symptoms repeated epistaxis, nasal congestion, nasal discharge and hearing loss. A skull X-ray or a CT scan of the head can confirm the presence of an angiofibroma. Treatment may include the surgical removal of the lesion if it is enlarging or blocking the airway. (27 Sep 1997) |
| juvenile arrhythmia | <cardiology, physiology> An increase in heart rate during inspiration. A normal physiologic response, more pronounced in children. (27 Sep 1997) |
| juvenile carcinoma | <tumour> Carcinoma of the breast with pale-staining cells showing prominent secretory activity, as seen in pregnancy and lactation, but found mostly in children. Synonym: juvenile carcinoma. (05 Mar 2000) |
| juvenile cataract | A soft cataract occurring in a child or young adult. (05 Mar 2000) |
| juvenile cerebellar astrocytoma | <oncology, tumour> This primary brain tumour of the cerebellum accounts for 10 to 30% of brain tumours in children. The are usually slow growing and benign. Symptoms include gait problems, clumsiness, headache and vomiting. Treatment often involves a combination of surgery, radiation therapy and chemotherapy. (27 Sep 1997) |
| juvenile chorea | A postinfectious chorea appearing several months after a streptococcal infection with subsequent rheumatic fever. The chorea typically involves the distal limbs and is associated with hypotonia and emotional lability. Improvement occurs over weeks or months and exacerbations occur without associated infection recurrence. Synonym: acute chorea, chorea minor, chorea, juvenile chorea, rheumatic chorea, Sydenham's disease. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|