| 영문 | spinal tap, spinal puncture | 한글 | 허리천자, 요추천자, 요추뚫기 |
|---|---|---|---|
| 설명 | 질병의 진단이나 치료 또는 마취를 하기 위해 피부에서 거미막밑공간으로 바늘을 찌를 때가 있다. 이것은 셋째 허리뼈 아래쪽에서 시행한다. 척수가 첫째 허리뼈 아랫모서리에서 끝나고, 거미막밑공간은 둘째 엉치뼈 분절까지 뻗어 있기 때문에 이 부위는 바늘로 척수를 찌를 위험이 없다. 또 척추뼈고리판이 짧아 서로 겹쳐있지 않기 때문에 허리뼈 사이로 바늘을 찌를 수 있다. 이 부위의 거미막밑공간에는 척수신경 뿌리가 있으나, 이들은 뇌척수액속에 있기 때문에 바늘을 넣을 때 한쪽으로 밀려 손상받는 경우는 거의 없다. 배를 넓적다리에 붙일정도로 허리를 구부리면 고리판 사이가 더 벌어져 틈이 커진다. 바늘이 뚫고 지나가는 구조는 바깥에서 속으로 ① 피부, ② 피부밑조직, ③ 근육막, ④ 가시끝인대, ⑤ 가시사이인대, ⑥ 황색인대, ⑦ 경질막, ⑧ 거미막, ⑨ 뇌척수액이 된다.  |
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| 영문 | spinal cord | 한글 | 척수 |
|---|---|---|---|
| 설명 | 척추내에 위치하는 중추신경계의 일부분. 위에서부터 목척수, 등척수, 허리척수, 엉치척수로 구분됨. 내부는 바깥쪽의 백색질과 안쪽의 회색질로 구분된다. 척수의 아래끝은 척수 원뿔이라 하며 첫번째 허리뼈 높이까지 내려온다. 뇌와 말초신경사이의 신경 통로 역할을 하며 척수반사(예: 무릎반사)에서는 뇌를 통하지 않고 반사의 중추 작용을 한다.  |
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| 영문 | spinal nerve | 한글 | 척수신경 |
|---|---|---|---|
| 설명 | 척수의 앞뿔에서 출발하는 운동신경과 뒷뿔으로 들어오는 감각신경이 합쳐서 형성되는 신경으로서 총 31쌍이 존재함. 목뼈신경이 8쌍, 자등뼈신경이 12쌍, 허리뼈의 신경이 5쌍, 엉치뼈의 6쌍을 이룸. |
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| SPA | salt-poor albumin; sheep pulmonary adenomatosis; sperm penetration assay; spinal progressive amyotro... |
|---|---|
| PSA | parasternal short axis; pleomorphic salivary gland adenoma; polyethylene sulfonic acid; polysacchari... |
| PMD | Progressive Muscular Dystrophy; 진행성 근이영양증 Types of PMD(Progressive Muscular Dystroph... |
| PML | peripheral motor latency; polymorphonuclear leukocyte; posterior mitral leaflet; progressive multifo... |
| PR | by way of the rectum [Lat. per rectum]; far point [of accommodation] [Lat. punctum remotum]; palindr... |
| HNA | Hereditary Neuralgic Amyotrophy |
|---|---|
| CPEO | Chronic Progressive External Ophthalmoplegia |
| OPP | Ovine progressive pneumonia |
| PPA | Primary Progressive Aphasia |
| PAL | progressive addition lens |
| progressive spinal amyotrophy | A serious neurologic disease that results from the progressive degeneration of the motor neurons. (27 Sep 1997) |
|---|
| 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 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) |
| amyotrophy | A type of diabetic neuropathy that causes muscle weakness and wasting. (09 Oct 1997) |
| hemiplegic amyotrophy | Muscular atrophy seen in hemiplegic limbs. (05 Mar 2000) |
| neuralgic amyotrophy | A neurological disorder, of unknown cause, characterised by the sudden onset of severe pain, usually about the shoulder and often beginning at night, soon followed by weakness and wasting of various forequarter muscles, particularly shoulder girdle muscles; both sporadic and familial in occurrence with the former much more common; often preceded by some antecedent event, such as an upper respiratory infection, hospitalization, vaccination, or non-specific trauma; usually attributed to a brachial plexus lesion, because the nerve fibres involed are most often derived from the upper trunk, but actually multiple proximal mononeuropathies. Synonym: acute brachial radiculitis, brachial plexitis, brachial plexus neuropathy, Parsonage-Turner syndrome, shoulder-girdle syndrome. (05 Mar 2000) |
| diabetic amyotrophy | A type of diabetic neuropathy that primarily affects elderly patients with diabetes mellitus; clinically characterised by unilateral or bilateral anterior thigh pain, weakness, and atrophy; of abrupt or gradual onset and, when bilateral, of simultaneous or sequential onset, and usually asymmetrical; one type of diabetic polyradiculopathy. Sometimes referred to, erroneously, as diabetic femoral neuropathy. (05 Mar 2000) |
| 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) |
| rapidly progressive glomerulonephritis | <nephrology> A relatively uncommon (affecting 1 out of 10,000 people) form of acute glomerulonephritis that results in damage within the glomerulus of the kidney. There is rapid loss of kidney function with the formation of crescents on microscopic analysis (kidney biopsy). This disorder may result in acute glomerulonephritis or nephrotic syndrome, but ultimately results in renal failure and end-stage renal disease. Symptoms include smoky coloured urine (pyuria), decreased urine output, swelling and hypertension. Any conditions which can cause a vasculitis increase the risk of this disorder. Some examples include lupus, Goodpasture's syndrome, Henoch-Schonlein purpura, IgA nephropathy, membranoproliferative glomerulonephritis, anti-glomerular basement membrane antibody disease, history for malignant tumours and exposure to hydrocarbon solvents. (27 Sep 1997) |
| chronic progressive chorea | A progressive disorder usually beginning in young to middle age, consisting of a triad of choreoathetosis, dementia, and autosomal dominant inheritance with complete penetrance. Bilateral marked wasting of the putamen and the head of the caudate nucleus is characteristic. Synonym: chronic progressive chorea, degenerative chorea, hereditary chorea, Huntington's disease. (05 Mar 2000) |
| chronic progressive external ophthalmoplegia | A specific type of slowly worsening weakness of the ocular muscles, usually associated with a pigmentary retinopathy. See: Kearns-Sayre syndrome, oculopharyngeal dystrophy. Synonym: ocular myopathy. (05 Mar 2000) |
| chronic progressive syphilitic meningoencephalitis | Syphilitic infection manifested as dementia (often with delusional features), dysarthria, seizures, myoclonic jerks, action tremor, impaired walking and standing, pupillary abnormalities, and abnormal CSF findings. Synonym: chronic progressive syphilitic meningoencephalitis. (05 Mar 2000) |
| pneumonia, progressive interstitial, of sheep | Chronic respiratory disease caused by the visna-maedi virus. It was formerly believed to be identical with jaagsiekte (pulmonary adenomatosis, ovine) but is now recognised as a separate entity. (12 Dec 1998) |
| primary progressive cerebellar degeneration | A familial ataxic condition related to cerebellar degeneration. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|