| 영문 | cardiovascular system | 한글 | 심장혈관계 |
|---|---|---|---|
| 설명 | 신체의 혈액순환을 담당하는 기관. 즉 심장과 혈관을 통칭해서 이르는 말이다. |
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| 영문 | autonomic nervous system | 한글 | 자율신경계 |
|---|---|---|---|
| 설명 | 사람의 의지와 관계없이, 침을 흘리거나 소화운동 등과 같은 스스로 조정이 되어 움직이는 신경계이며 여기에는 다음과 같은 두 가지가 있다. 1.교감신경계(sympathetic nervous system)-사람이 위험상태에 이르렀을 경우에 흥분이 되는 자율신경계. 즉 심박수의 증가, 소화기 운동의 감소 등의 일이 이곳을 통해서 일어난다. 교감신경이 흥분되면 교감신경의 말단에서 epinephrine, norepinephrine 등의 물질이 분비되고 이것들에 의해서 말초장기가 변화를 일으킨다. 하지만 장기에 따라서 epinephrine이나 norepinephrine의 수용체를 가지고 있어서 여러 가지 다른 장기의 반응을 볼 수가 있다. 수용체는 다음과 같다. -알파수용체(alpha-receptor): 말초혈관의 수축, 기관지의 수축, 동공의 근육의 수축 -베타1수용체(beta 1-receptor): 심장에 존재하는 수용체, 심장을 빨리 뛰게하는 역할을 한다. -베타2수용체(beta 2-receptor): 혈관의 이완, 기관지의 이완, 즉 각 장기들은 그 장기가 가지고 있는 교감신경의 수용체에 따라 교감신경의 흥분(교감신경 말단에서의 epinephrine의 분비)에 대한 반응이 달라진다(예-교감신경이 흥분시에 beta 1-수용체를 가지고 있는 심장은 빨리 뛰게 된다. 교감신경 흥분시에 동공의 근육이 수축해서 동공의 크기가 커진다) 2.부교감신경계(parasympathetic nervous system)-교감신경과 반대로 작용한다. 즉 사람이 졸리거나 쉴 경우에 흥분한다. 부교감신경이 흥분할 때에는 신경의 말단에서 아세칠콜린의 분비가 일어나고 이것으로 인해서 각 장기의 변화가 일어난다. |
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| 영문 | TNM staging system | 한글 | 종양병기분류계통 |
|---|---|---|---|
| 설명 | 종양의 병기(stage)를 결정하는 한 방법. T는 Tumor(종양)를 뜻하며 원발병터의 크기, 주위조직으로의 침윤정도 등에 따라 T1, T2, T3, T4(숫자가 높을 수록 주위로 침윤이 많다) 등으로 나눈다. N은 Node(림프절)를 뜻하며 침범된 림프절의 갯수, 크기, 위치 등에 따라 N1, N2, N3 등으로 나눈다. M은 Metastasis(전이)를 뜻하며 원격전이의 유무에 따라 M0, M1 등으로 나눈다. 이상의 방법으로 T, N, M이 결정되면 이들을 조합하여 최종적인 병기를 결정한다. 이렇게 결정된 병기는 치료 방침 결정과 예후 판단에 매우 중요하다. |
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| 영문 | central nervous system(CNS) | 한글 | 중추신경계 |
|---|---|---|---|
| 설명 | 신경계는 중추신경계와 말초신경계로 분류할 수가 있다. 중추신경계란 뇌와 척수로 구성되어 있는 신경계를 이르는 말이다. 말초신경계란 이 이외의 모든 신경계를 이르는 말이다. |
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| CHD | Chediak-Higashi disease; childhood disease; chronic hemodialysis; congenital or congestive heart dis... |
|---|---|
| MDS | Master of Dental Surgery; maternal deprivation syndrome; medical data screening; medical data system... |
| MPS | meconium plug syndrome; medial premotor system; Member of the Pharmaceutical Society; microbial prof... |
| CNS | central nervous system; clinical nurse specialist; coagulase-negative staphylococci; congenital neph... |
| CRS | Carroll rating scale for depression; catheter-related sepsis; caudal regression syndrome; cervical s... |
| congenital erythropoietic porphyria | A group of metabolic disorders that result from a disturbance in porphyrin metabolism, causing increased formation and excretion of porphyrin or its precursors. Acute intermittent porphyria is a rare inherited (autosomal dominant) form that can result in abdominal pain, photosensitivity and neurological disturbances. The various forms can be differntiated measuring various blood prophyrins. Inheritance: autosomal dominant. (27 Sep 1997) |
|---|---|
| congenital facial diplegia | <syndrome> A developmental bilateral facial paralysis usually associated with oculomotor or other neurological disorders. Synonym: congenital facial diplegia. (05 Mar 2000) |
| congenital fibrosis of the extraocular muscles | An autosomal dominant disorder associated with blepharoptosis and absence of eye movements. (05 Mar 2000) |
| congenital generalised fibromatosis | Multiple subcutaneous and visceral fibrous tumours present at birth; a rare disorder often fatal in the first week of life, although sometimes undergoing spontaneous remission; probable autosomal recessive inheritance. (05 Mar 2000) |
| congenital giant pigmented nevus | These large pigmented (often hairy) congenital nevi are important because of their increased risk (10 to 15%) of conversion into malignant melanoma. A biopsy can confirm if cells have turned malignant. Any change in a pre-existing nevus should prompt a physician evaluation. (27 Sep 1997) |
| congenital glaucoma | An affection of infancy, marked by an increase of intraocular pressure with enlargement of the eyeball. Synonym: congenital glaucoma, hydrophthalmia, hydrophthalmos, hydrophthalmus. Origin: G. Bous, ox, + ophthalmos, eye (05 Mar 2000) |
| congenital haemolytic anaemia | Accelerated destruction of red blood cells due to an inherited defect, such as in the membrane in hereditary spherocytosis. (05 Mar 2000) |
| congenital haemolytic icterus | <haematology> A hereditary disorder that leads to a chronic haemolytic anaemia due to an abnormality in the red blood cell membrane. This disorder is caused by a defective gene. Red cells are resistant to stress and rupture easily. Infants may appear jaundiced and pale. Fatigue, weakness and shortness of breath are other symptoms that may be seen in older patients. The spleen may also be enlarged. Treatment includes splenectomy (removal of the spleen). After this is accomplished the life-span of the red blood cells returns to normal. (27 Sep 1997) |
| congenital haemolytic jaundice | <haematology> A hereditary disorder that leads to a chronic haemolytic anaemia due to an abnormality in the red blood cell membrane. This disorder is caused by a defective gene. Red cells are resistant to stress and rupture easily. Infants may appear jaundiced and pale. Fatigue, weakness and shortness of breath are other symptoms that may be seen in older patients. The spleen may also be enlarged. Treatment includes splenectomy (removal of the spleen). After this is accomplished the life-span of the red blood cells returns to normal. (27 Sep 1997) |
| congenital heart block | Atrioventricular block present in utero or at birth and usually of advanced or complete degree. (05 Mar 2000) |
| congenital heart disease | Heart disease that is present from birth. Examples include atrial septal defect, ventricular septal defect, aortic stenosis and tetralogy of Fallot. (27 Sep 1997) |
| congenital hernia of the diaphragm | A condition present at birth where there is abnormal protrusion of abdominal contents upward through a defect in the diaphragm. This condition is treated as a surgical emergency due to interference with the infant's breathing. Smaller, less serious diaphragmatic hernias may also be seen in adults. (27 Sep 1997) |
| congenital hip dislocation | A malformation of the hip joint that is present at birth. Genetic factors likely play a role in this disorder. Features include hip dislocation, asymmetry of leg positions, asymmetric fat folds and diminished movement on the affected side. Some children will exhibit little or no features and must be diagnosed by physical examination of the hip joints. (27 Sep 1997) |
| congenital hip dysplasia | A malformation of the hip joint that is present at birth. Genetic factors likely play a role in this disorder. Features include hip dislocation, asymmetry of leg positions, asymmetric fat folds and diminished movement on the affected side. Some children will exhibit little or no features and must be diagnosed by physical examination of the hip joints. Origin: Gr. Plassein = to form (27 Sep 1997) |
| congenital hydrocele | A collection of fluid in the unobliterated processus vaginalis leading from the abdominal cavity to the investing sac of the testis. (05 Mar 2000) |