| 영문 | cervical dysplasia | 한글 | 자궁목형성이상 |
|---|---|---|---|
| 설명 | 자궁목이란 자궁이 질과 연결된 부위로 자궁의 입구에 해당하는 부위이다. 이곳은 상피로 둘러쌓여 있다. 상피란 신체의 내부나 외부를 쌓고 있는 조직을 이르는 말로, 이 상피의 아래에는 대개 상피를 지지하고 있는 조직이 존재한다. 그리고 이 지지조직과 상피의 사이에는 기저막이라는 막이 있어서 상피와 지지조직을 구분한다. 자궁경부이형성이란 여러 가지 자극에 의해서 암성변화를 한 자궁상피의 세포가 자궁상피의 일부가 차지하고 있는 경우를 이르는 말이다. 즉 상피의 일부가 암성변화를 한 세포가 메우고 있는 것을 이른다. 이것 자체가 암은 아니지만 전암성 병변이며 이것이 계속 진 행이 되어 자궁상피의 전층을 암세포가 채우게 되면 이것을 상피내암종이라고 부르고 만약 더 진행이 되어서 암세포가 기저막을 뚫고 상피밑의 지지 조직을 침범한다면 이것을 침윤암이라고 부른다.  |
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| 영문 | cervical vertebra | 한글 | 목뼈, 경추 |
|---|---|---|---|
| 설명 | 척추 중에서 목부분을 이루는 척추뼈를 이르는 말이다. 척주의 시작인 첫번째 척추뼈에서부터 7번째 척추뼈까지를 말한다. 목있는 폴립(sessile polyp) 기시부가 넓은 모양을 가지고 내강내로 돌출되어 나온 폴립을 말한다. 이에 비해 좁은 줄기에 의해 지탱되는 폴립을 목있는 폴립이라 한다. |
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| 영문 | fibrous dysplasia | 한글 | 섬유형성이상 |
|---|---|---|---|
| 설명 | 국소 발육장애로 뼈의 모든 성분이 나타나나 성숙한 구조로 분화하지는 못하는 병이다. 임상으로 하나의 뼈 혹은 여러개의 뼈를 동시에 침범할 수 있다. 여러뼈 유형은 갈색색소 침착과 내분비 장애를 동반하며 조숙한 성적 발육을 동반한다. 육안소견으로 경계가 뚜렷한 병터로 조직소견으로는 섬유모세포의 증식과 곡선상의 뼈잔기둥으로 구성되어 있는데 뼈잔기둥은 뼈모세포로 덮여있지 않은 무층뼈(woven bone)이다. |
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| CIN1, | CIN I cervical intraepithelial neoplasia, grade 1 (mild dysplasia) |
|---|---|
| C. | 1) Candida C. Albicans C. Guillier... |
| HIVD | Herniation(Herniated) of Inter-Vertebral Disc - Cervical HIVD &... |
| C1 | first cervical nerve; first cervical vertebra; first component of complement |
| C2 | second cervical nerve; second cervical vertebra; second component of complement |
| CMS | Chronic mild stress |
|---|---|
| MCI | Mild Cognitive Impairment |
| MTBI | Mild Traumatic Brain Injury |
| TOMHS | Treatment Of Mild Hypertension Study |
| MHI | mild head injury |
| mild | Gentle; pleasant; kind; soft; bland; clement; hence, moderate in degree or quality; the opposite of harsh, severe, irritating, violent, disagreeable, etc.; applied to persons and things; as, a mild disposition; a mild eye; a mild air; a mild medicine; a mild insanity. "The rosy morn resigns her light And milder glory to the noon." (Waller) "Adore him as a mild and merciful Being." (Rogers) Mild, or Low, steel, steel that has but little carbon in it and is not readily hardened. Synonym: Soft, gentle, bland, calm, tranquil, soothing, pleasant, placid, meek, kind, tender, indulgent, clement, mollifying, lenitive, assuasive. See Gentle. Origin: AS. Milde; akin to OS. Mildi, D. & G. Mild, OHG. Milti, Icel. Mildr, Sw. & Dan. Mild, Goth. Milds; cf. Lith. Melas dear, Gr. Gladdening gifts. Source: Websters Dictionary (01 Mar 1998) |
|---|---|
| mild foetal bradycardia | A foetal heart rate less than 120 beats per minute. (05 Mar 2000) |
| mild mercurial ointment | A grease-based ointment containing 20% finely divided metallic mercury, formerly widely used for local application to the skin for the destruction of body lice. Risk is associated with transdermal absorption of mercury and a local dermatitis. Synonym: mild mercurial ointment. (05 Mar 2000) |
| mild silver protein | A complex prepared by the reaction of silver oxide with either gelatin or serum albumin. Black shiny crystals liberate silver and it was formerly widely used as a topical anti-infective on mucous membranes. Contains from 19 to 25% silver, only a small fraction of which is ionizable. Can produce black or brown pigmentation due to deposition of reduced silver in the tissues. Synonym: argyrol, silvol. (05 Mar 2000) |
| cervical dysplasia | A term which describes precancerous changes to the epithelial cells lining the cervix. The diagnosis is made from the microscopic examination of a PAP smear acquired tissue specimen. Less than 5% of all PAP smears will show cervical dysplasia. The peak incidence is in women 25 to 35 years of age. Risk factors include multiple sexual partners, early onset of sexual activity (less than 18), early childbearing (less than 16) and past medical history of a sexually transmitted disease (for example genital warts, genital herpes, HIV infection). Treatment is based on the degree of dysplasia present, as judged by a pathologist. Treatments include cryotherapy and conisation. Origin: Gr. Plassein = to form (27 Sep 1997) |
| anhidrotic ectodermal dysplasia | A hereditary condition (most often x linked) that is characterised by the abnormal development of skin, absence of sweat glands, dry eyes and abnormal development of teeth. Symptoms include absent teeth, peg teeth, inability to sweat, thin skin and heat intolerance. Mucous membrane involvement may result in a foul-smelling nasal discharge. The inability to sweat leads to the inability to maintain normal body temperature in a warm environment. Some may exhibit fevers and will require artificial cooling. Inheritance: mostly sex-linked (X chromosome). Origin: Gr. Plassein = to form (12 Nov 1997) |
| anterofacial dysplasia | Abnormal growth of the face or cranium in an anteroposterior direction as seen and measured with a cephalogram. (05 Mar 2000) |
| arrhythmogenic right ventricular dysplasia | A congenital cardiomyopathy in which transmural infiltration of adipose tissue results in weakness and aneurysmal bulging of the infundibulum, apex, and posterior basilar region of the right ventricle and leads to ventricular tachycardia arising in the right ventricle. (12 Dec 1998) |
| asphyxiating thoracic dysplasia | Hereditary hypoplasia of the thorax, associated with pelvic skeletal abnormality. Synonym: asphyxiating thoracic chondrodystrophy, Jeune's syndrome, thoracic-pelvic-phalangeal dystrophy. (05 Mar 2000) |
| bronchopulmonary dysplasia | <embryology, paediatrics> A form of chronic lung disease of uncertain cause sometimes seen in children who have received mechanical respiratory support (with high oxygenation) in the neonatal period. Often associated with those infants who have been treated for hyaline membrane disease. Origin: Gr. Plassein = to form (27 Sep 1997) |
| mammary dysplasia | An obsolete term for fibrocystic condition of the breast. (05 Mar 2000) |
| mandibulofacial dysplasia | A hereditary disorder occurring in two forms: the complete form (franceschetti's syndrome) is characterised by antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia and hypoplasia of the zygomatic arches, and microtia. It is transmitted as an autosomal trait. The incomplete form (treacher collins syndrome) is characterised by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (12 Dec 1998) |
| ventriculoradial dysplasia | A congenital syndrome consisting of a ventricular septal defect with associated absence of thumb or radius. (05 Mar 2000) |
| cerebral dysplasia | Abnormal development of the telencephalon. (05 Mar 2000) |
| retinal dysplasia | <ophthalmology> Congenital, often bilateral, retinal abnormality characterised by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|