| 영문 | atrophy | 한글 | 위축(증) |
|---|---|---|---|
| 설명 | 조직이나 세포 혹은 기관의 크기가 원래의 크기에 비하여 줄어드는 것을 일컫는 말. 처음부터 크기가 작은 무형성/형성저하증(aplasia/hypoplasia)와 구별된다. |
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| 영문 | cerebral infarction | 한글 | 뇌경색증 |
|---|---|---|---|
| 설명 | 급격한 혈액 공급의 차단으로 인해서 조직이 죽는 것을 말한다. 뇌경색증은 뇌의 조직이 혈류의 급격한 차단에 의해서 죽은 것을 말한다. 혈류가 완전히 차단되면 국소에 혈액이 없어지므로 그 조직에 경색이 생기게 된다. 경색이 생긴 부위는 혈액의 공급이 없으므로 원칙적으로는 정상적으로 혈류가 공급되는 부위보다 창백하고 희게 보인다. 이런 부분을 백색경색(white infarct) 또는 빈혈경색(anemic infarct)라 한다. 하지만 이 부위에 이차적으로 적혈구가 빠져 들어가면 그 부위는 피가 고이게 되고 적색을 띠게 된다. 이런 부분을 적색경색(red infarct) 또는 출혈경색(hemorrhagic infarct)이라고 한다. 뇌의 경색증에는 이 두 가지 모두 발생가능하다. |
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| 영문 | cerebral aneurysm | 한글 | 뇌동맥류, 뇌동맥자루 |
|---|---|---|---|
| 설명 | 뇌의 동맥에 생긴 동맥자루. 임상적으로 중요시되는 이유는 이것이 잘 터져 뇌출혈의 중요한 원인이 되기 때문이다. 대부분의 동맥자루가 출혈을 일으키지만 출혈을 일으키지 않는 경우에는 주위의 뇌 조직의 압박에 의해서 두통이나 발작 등을 일으킬 수 있다. |
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| 영문 | cerebral palsy | 한글 | 뇌성마비 |
|---|---|---|---|
| 설명 | 출생전, 출생시 혹은 출생후의 뇌의 선천기형, 손상 혹은 중추신경계의 병에 의해서 영구적이며, 비진행성인 운동신경 및 정신장애를 일으키는 경우를 뜻한다. 원인은 여러 가지가 있을 수 있으나 조산으로 인한 뇌의 산소공급의 부족, 또는 난산으로 인한 호흡장애 등이 흔한 원인이다. 증상은 대개 비진행성의 뇌 병변으로 인한 운동장애가 대표적인 증상이며 그외에 청력, 시력의 장애, 지능부전, 언어장애, 경련 및 정신장애 등이 동반될 수 있다. |
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| 영문 | cerebral contusion | 한글 | 뇌좌상 |
|---|---|---|---|
| 설명 | 외부에서 기원하는 물리적 충격에 의한 뇌의 물리적 손상. |
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| CA | anterior commissure [Lat. commissura anterior]; calcium antagonist; California [rabbit]; cancer; Can... |
|---|---|
| PMA | index of prevalence and severity of gingivitis, where P = papillary gingiva, M = marginal gingiva, a... |
| PPMA | progressive postmyelitis muscular atrophy |
| SPMA | spinal progressive muscular atrophy |
| PMD | Progressive Muscular Dystrophy; 진행성 근이영양증 Types of PMD(Progressive Muscular Dystroph... |
| PRA | Progressive retinal atrophy |
|---|---|
| PMA | progressive muscular atrophy |
| CA | Cerebral atrophy |
| CA | Cerebellar atrophy |
| DRPLA | Dentato-rubral and pallido-luysian atrophy |
| progressive circumscribed cerebral atrophy | Circumscribed atrophy of the cerebral cortex. Synonym: lobar sclerosis, progressive circumscribed cerebral atrophy. (05 Mar 2000) |
|---|
| progressive choroidal atrophy | An x chromosome-linked abnormality characterised by atrophy of the choroid and degeneration of the retinal pigment epithelium causing night blindness. (12 Dec 1998) |
|---|---|
| progressive infantile spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| progressive muscular atrophy | A serious neurologic disease that results from the progressive degeneration of the motor neurons. (27 Sep 1997) |
| progressive spinal muscular atrophy | One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of the spinal cord, manifested as progressive, often symmetrical, weakness and wasting, typically beginning in the distal portions of the limbs, particularly in the upper extremities, and spreading proximally; fasciculation potentials are often present, but evidence of corticospinal tract disease (e.g., increased deep tendon reflexes, Babinski sign) is not. (05 Mar 2000) |
| infantile progressive spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| essential progressive atrophy of iris | Progressive atrophy of the iris without inflammatory signs, characterised by patchy loss of all layers of the iris with hole formation, migration of the pupil, degeneration of the corneal endothelium, peripheral anterior synechiae, and secondary glaucoma; usually unilateral, predominantly affecting women in their middle years. (05 Mar 2000) |
| progressive cerebral poliodystrophy | Familial progressive spastic paresis of extremities with progressive mental deterioration, with development of seizures, blindness and deafness, beginning during the first year of life, and with destruction and disorganization of nerve cells of the cerebral cortex. Synonym: Alpers disease, Christensen-Krabbe disease, progressive cerebral poliodystrophy. (05 Mar 2000) |
| circumscribed | Limited in space, well localised. (27 Sep 1997) |
| circumscribed breast lesions | <radiology> Lucent, lipoma, oil cyst (following haematoma or biopsy), galactocele (associated with lactation), mixed density, fibro-adeno-lipoma, galactocele, intramammary lymph node, haematoma (12 Dec 1998) |
| circumscribed craniomalacia | A disease marked by the presence of areas of thinning and softening in the bones of the skull and widening of the sutures and fontanelles. Usually of syphilitic or rachitic origin. Synonym: circumscribed craniomalacia. Origin: cranio-+ L. Tabes, a wasting (05 Mar 2000) |
| circumscribed peritonitis | Peritonitis confined to a demarcated region of the peritoneal cavity. Synonym: circumscribed peritonitis. (05 Mar 2000) |
| circumscribed pyocephalus | Abscess of the brain. (05 Mar 2000) |
| scleroderma, circumscribed | A chronic, localised hardening and thickening of the skin. Lesions may be categorised as morphea (guttate, profunda, pansclerotic) or linear (with or without melorheostosis or hemiatrophy). It is twice as common in women as in men. The condition is characterised by skin ischemia, lymphocytic infiltrates, swollen collagen bundles, and thickening of the dermis with reduction of subcutaneous fat. (12 Dec 1998) |
| aphasia, primary progressive | A type of aphasia appearing gradually and gradually worsening without any major change in other cognitive functions. It is regarded by some authors as a syndrome which may be due to various degenerative diseases of the cerebral cortex (notably alzheimer disease, owing to its frequency), while others see in it an autonomous disease related to a neuropathological process that is distinct from the main degenerative dementias. The principal clinical peculiarity of primary progressive aphasia is that it spares the patient's autonomy for a long time, but ultimately turns into global dementia. (12 Dec 1998) |
| bovine progressive degenerative myeloencephalopathy | A familiar myeloencephalopathy of brown Swiss cattle characterised by bilateral hindleg weakness and ataxia and deficient proprioceptive reflexes. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|