| 영문 | Dilatation and Curettage(D & C) | 한글 | 자궁긁어냄술, 자궁목확장 |
|---|---|---|---|
| 설명 | 자궁이란 태아가 수태되어서 분만전까지 발육하고 성장하는 공간이다. 자궁속에 병변이 있어 임신이 계속될 수 없거나 아니면 다른 이유로 임신되어 있는 태아를 제거하고자 할 경우에 사용되는 방법이다. 여기서 긁어내기 위하여는 우선 자궁의 입구에 해당하는 자궁목을 확장시켜야 한다. 여기에는 급속히 확장을 시도하는 법과 서서히 확장을 시도하는 2가지 방법이 있다. 자궁목을 급속히 확장할 때는 헤가르 목관확장기(Hegar's dilatator)를 사용한다. 이것은 작은 금속막대로 작은 크기부터 큰 크기까지 다양한 크기가 있어서 우선 작은 막대로 시작하여 점점 큰 크기의 막대를 자궁목에 넣어서 자궁목을 확장시킨다. 서서히 확장시킬 때는 Laminaria tent를 목관에 삽입하는 방법을 사용한다. Laminaria tent란 해초로 만든 작은 막대로 수분을 흡수하면 점점 늘어나는 성질이 있다. 이것을 자궁의 목에 넣으면 이것이 수분을 흡수하여 늘어나므로 천천히 자궁의 목이 늘어난다. 자궁목이 충분히 늘어나면 그 속으로 끝이 숟가락처럼 생긴 기구를 넣어서 자궁속의 병변이나 임신된 태아를 긁어내는데 여기에 사용되는 숟가락처럼 생긴 기구를 큐렛이라고 한다. 초기 임신중절 즉 유산과 같은 임신과 관련된 경우뿐만 아니라, 비임신 자궁의 자궁내막조직의 채취 및 제거를 위해서도 행해지는 수기이다. 이는 원칙적으로 마취하에 실시되는 것으로 자궁목관을 확장하고 기구로 자궁 내용물을 제거하고 큐렛으로 자궁내벽을 깨끗이 한다. 자궁천공이나 자궁목의 파열 등의 위험이 따르며, 수술후 감염 또는 출혈 등에 대한 주의가 필요하다. |
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| 영문 | congenital syphilis | 한글 | 선천매독 |
|---|---|---|---|
| 설명 | 임부가 매독에 감염되어 있으면 임신 후기에 매독균이 태반을 통해 혈행성으로 태아에 감염(수직감염)된 것을 말하다. 대부분은 유산, 사산이 되지만 출생하면 제2기 이후의 발진을 보인다. 발현시기에 따라서 ① 태아매독, ② 유아매독, ③ 만발성 선천매독으로 분류된다. ①에서는 뼈연골염, 간-지라 비대와 매독성 천포창, ②에서는 파로가성마비와 매독성 코염, ③에서는 허친슨 세징후(허친슨 치아, 속귀성 난청, 실질성 각막염)에 따라 특징이 있다. 기타 수두증, 지능발육 불량 등을 자주 볼 수 있다. 매독 혈청반응은 대부분의 경우 양성으로 나온다. 매우 드물게 간세포내에서 매독균을 무수히 볼 수 있다. 간세포 주변의 섬유화와 함께 불규칙한 흉터(hepar lobatum)를 만들 수 있다. |
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| 영문 | congenital rubella syndrome | 한글 | 선천풍진증후군 |
|---|---|---|---|
| 설명 | 임신기간 중에 산모가 풍진에 걸리면 이 풍진 바이러스는 태반을 통해서 태아에게 전달되어서 태아의 풍진감염을 일으킨다. 임신 첫 3개월 동안, 특히 임신 첫달에 태아가 풍진의 감염을 받으면, 신생아에서 선천기형, 즉 눈에서 촛점을 정확히 맞추어주는 렌즈의 역할을 하는 수정체의 혼탁(백내장), 심장기형, 귀머거리 및 심한 지능박약을 동반하는 소두증 등이 발생하는 수가 많다. |
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| 영문 | congenital heart disease | 한글 | 선천심장병 |
|---|---|---|---|
| 설명 | 선천적으로 심장의 구조에 이상이 있는 병. |
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| TTA | tetanus toxoid antibody; timed therapeutic absence; total toe arthroplasty; transtracheal aspiration... |
|---|---|
| CAV | congenital absence of vagina; congenital adrenal virilism; constant angular velocity; croup-associat... |
| CDH | 1) Chronic Daily Headache = CTH = ... |
| CDH | ceramide dihexoside; congenital diaphragmatic hernia; congenital dislocation of hip; congenital dysp... |
| CALP | congenital absence of left pericardium |
| CAVD | Congenital absence of the vas deferens |
|---|---|
| CBAVD | Congenital bilateal absence of the vas deferens |
| TOE | Transesophageal echocardiography |
| FMD | Foot and Mouth Disease |
| FMDV | Foot and Mouth Disease Virus |
| congenital absence of pulmonary valve | <radiology> BIG central pulmonary arteries, big RV (12 Dec 1998) |
|---|---|
| foot deformities, congenital | Alterations or deviations from normal shape or size which result in a disfigurement of the foot occurring at or before birth. (12 Dec 1998) |
| absence | Paroxysmal attacks of impaired consciousness, occasionally accompanied by spasm or twitching of cephalic muscles, which usually can be brought on by hyperventilation; depending on the type and severity of the absence, the EEG may show an abrupt onset of a 3/sec spike and wave pattern as in simple absence, or in atypical cases, a 4/sec spike and wave or faster spike complexes. The clinical states accompanying these EEG abnormalities may be classified as: 1) absence with no overt manifestations, e.g., simple absence; epileptic absence; subclinical absence; 2) absence with clonic movements, e.g., myoclonic absence; 3) absence with atonic states, e.g., atonic absence; 4) absence with tonic contractions, e.g., hypertonic muscular contraction; 5) absence with automatisms, e.g., various stereotyped movements, usually of the face or hands; 6) absence with atypical features, e.g., bizarre motor activity. Origin: L. Absentia (05 Mar 2000) |
| absence seizure | <neurology> A type of seizure that in contrast to the grand mal seizure, are noted for their brevity and for the degree of loss of awareness (brief staring spell) accompanied by minimal motor manifestations. A common form of childhood epilepsy. (06 Oct 1997) |
| atypical absence seizure | An absence seizure associated with an EEG pattern of irregular or slow spike and wave at less than 2.5 Hz or paroxysmal fast activity on an abnormally slow background EEG. (05 Mar 2000) |
| childhood absence epilepsy | A generalised epilepsy syndrome characterised by the onset of absence seizures in childhood, typically at age six or seven years. There is a strong genetic predisposition and girls are affected more often than boys. EEG reveals generalised 3 Hz spike-wave activity on a normal background. Prognosis for remission is good if the patient does not also have generalised tonic-clonic seizures. See: absence. Synonym: petit mal epilepsy, pyknolepsy. (05 Mar 2000) |
| pure absence | A brief clouding of consciousness accompanied by the abrupt onset of 3/sec spikes and waves on EEG. Synonym: pure absence. (05 Mar 2000) |
| simple absence | A brief clouding of consciousness accompanied by the abrupt onset of 3/sec spikes and waves on EEG. Synonym: pure absence. (05 Mar 2000) |
| epilepsy, absence | Epileptic seizures that consist of a sudden cessation of ongoing conscious activity without convulsive muscular activity or loss of postural control. These seizures may be so brief as to be inapparent, lasting seconds and occasionally several minutes. Absence seizures usually begin in otherwise neurologically normal children and rarely appear for the first time in adults. The seizures may occur hundreds of times per day and go on for weeks or months before it is recognised that a child is having seizures. (12 Dec 1998) |
| 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) |
| hand-and-foot syndrome | <syndrome> Recurrent painful swelling of the hands and feet occurring in infants and young children with sickle cell anaemia. Synonym: sickle cell dactylitis. (05 Mar 2000) |
| hand-foot-and-mouth disease | <infectious disease> Hand, foot and mouth disease is a mild, highly infectious viral disease of children, characterised by vesicular lesions in the mouth and on the hands and feet. Occurs most often in young children (under 3) and is transmitted via close contact. Outbreaks occur most often in the spring. Usually begins as a throat infection (pharyngitis) that later includes a rash (blisters) on the hands, feet and diaper area. Blisters may also appear on the throat and in the mouth. Other features include anorexia, headache and fever. The illness is typically self-limited, lasting 5-7 days. There is no specific treatment other than general supportive care. An exanthematous eruption of small, pearl-gray vesicles of the fingers, toes, palms, and soles, accompanied by often painful vesicles and ulceration of the buccal mucous membrane and the tongue and by slight fever; the disease lasts 4 to 7 days, and is usually caused by Coxsackie virus type A-16, but other types have been identified. (05 Mar 2000) |
| hand-foot-and-mouth disease virus | The virus causing hand-foot-and-mouth disease; chiefly type A16 but also types A4, A5, A7, A9, or A10 Entervirus coxsackievirus. (05 Mar 2000) |
| foot-and-mouth disease | <disease> A highly infectious disease of wide distribution and great economic importance, occurring in cattle, swine, sheep, goats and all wild and domestic cloven-footed animals caused by a picornavirus (genus Rhinovirus) and characterised by vesicular eruptions in the mouth, tongue, hoofs, and udder; humans are rarely affected. Synonym: aftosa. (05 Mar 2000) |
| foot-and-mouth disease virus | A picornavirus of the genus Rhinovirus causing foot-and-mouth disease of cattle, swine, sheep, goats, and wild ruminants; it has wide distribution throughout Africa and Asia, causing serious economic losses; the virus is spread by contamination of the animal environment with infected saliva and excreta. Synonym: FMD virus. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|