| 영문 | lead poisoning, saturinism | 한글 | 납중독 |
|---|---|---|---|
| 설명 | 용해성 납을 흡입하거나 삼킴으로써 유발되는 직업병. 급성과 만성이 있으며 대량으로 흡수하여 급성 위장염 증상을 나타내는 급성 중독은 오히려 드물고, 극소량(1일 1mg 이하)의 납을 장기간 지속적으로 섭취함으로써 생기는 만성이 더 심각하다. 납제련업-활판인쇄업-도장업-납유리제조업-축전지제조업 등 납 또는 납을 함유한 물질을 다루는 사람, 또 과거에는 연백을 사용한 분에 의한 화장독이 여성에게 나타나 문제가 되었으나, 오늘날에는 가솔린에 혼합된 안티녹제인 사에틸납으로 인한 중독이 주목되고 있다. 사에틸납 중독의 증상은 여러 가지인데, 빈혈이나 떨리는 증상이 비교적 초기에 나타나고 납선(잇몸에 납이 침착하여 청회백색으로 착색된다)이나 발작적 복통이 특징이다. 일반적으로 납의 증기나 가루가 기도를 통해 체내로 들어가는 경우가 도료-안료에 들어 있는 납이 피부나 소화관을 통해 침투하는 증례보다 증상이 심하다. |
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| 영문 | diabetic neuropathy | 한글 | 당뇨병신경병증 |
|---|---|---|---|
| 설명 | 오래된 당뇨의 합병증으로 발생한다. 대개 당뇨병에 이환된 경우 당뇨병 자체에 의한 병보다 오랜 기간후의 합병증에 의해 목숨을 잃는 경우가 많다. 초기에 당뇨병에서 혈중포도당농도를 잘 조절하는 경우 이런 합병증이 발생하는 경우가 낮으나, 그렇지 못한 경우 합병증 발생이 많다. 대개 한번 발생한 경우, 치료는 어렵고 그 진행 또한 늦출 수 없다고 한다. 증상은 감각의 저하를 가져와, 아픔을 잘 느끼지 못하므로 주위 물건이나 사람과 잘 부딪히고, 부딪힌 후에도 사실을 인지하지 못해 계속적인 외상을 받게 되므로 부딪히기 쉬운 관절이나, 발가락, 발목부분 등에 손상을 가져온다. |
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| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = EKG 1. Conducting System Structu... |
|---|---|
| AVR | Augmented Voltage Right arm Frank N. Wilson Lead I, II, III와 같은 크기의 E... |
| aVF | unipolar limb lead on the left leg in electrocardiography |
| aVL | unipolar limb lead on the left arm in electrocardiography |
| aVR | unipolar limb lead on the right arm in electrocardiography |
| ABLES | Adult Blood Lead Epidemiology and Surveillance program |
|---|---|
| BLL | Blood lead level |
| LEAD | Lower extremity arterial disease |
| TEL | Tetraethyl lead |
| AMAN | Acute Motor Axonal Neuropathy |
| lead neuropathy | A peripheral neuropathy reportedly seen in chronic lead intoxication; reputedly characterised by wrist-drop, but no convincing modern reports of this are available. (05 Mar 2000) |
|---|
| asymmetric motor neuropathy | Neuropathy in which the loss of function is more marked in the extremities of one side of the body, old term for diabetic polyradiculopathy. (05 Mar 2000) |
|---|---|
| autonomic neuropathy | <neurology, pathology> A group of symptoms which is caused by damage to the nerves which supply the internal organs. May be associated with diabetes, alcohol abuse, trauma (nerve injury) and the use of anticholinergic medications. Symptoms include abdominal swelling, heat intolerance, nausea, vomiting, impotence, diarrhoea, constipation, dizziness with standing, difficulty urinating and urinary incontinence. Origin: Gr. Pathos = disease (27 Sep 1997) |
| axillary neuropathy | <neurology, pathology> A condition involving dysfunction of the axillary nerve which normally supplies the deltoid and teres minor muscles and sensation to the lateral aspect of the shoulder. This condition is a type of peripheral neuropathy that may manifest as the result of a variety of disease processes or injuries. Conditions associated with axillary nerve dysfunction include mononeuritis multiplex, fracture of the humerus, abduction injury to the shoulder, pressure to the armpit from a cast, splint or crutches. Symptoms include numbness over the outer portion of the shoulder, shoulder weakness and difficulty lifting arm or objects over your head. An EMG, nerve conduction study or muscle biopsy can be helpful in making the diagnosis. Recovery is generally spontaneous if the underlying cause can be corrected and shoulder mobility is preserved. Corticosteroid injections may be indicated in some instances. Origin: Gr. Pathos = disease (27 Sep 1997) |
| brachial plexus neuropathy | 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) |
| giant axonal neuropathy | <paediatrics> A rare disorder beginning at or after the third year of life, and presenting clinically with kinky hair, progressive painless clumsiness, muscle weakness and atrophy, sensory loss, and areflexia. Pathologically, both myelinated and unmyelinated nerve fibres contain axonal spheroids packed with neurofilaments; sporadic in nature. (05 Mar 2000) |
| vitamin B12 neuropathy | A subacute or chronic disorder of the spinal cord, such as that occurring in certain patients with vitamin B12 deficiency, characterised by a slight to moderate degree of gliosis in association with spongiform degeneration of the posterior and lateral columns. Synonym: combined sclerosis, combined system disease, funicular myelitis, Putnam-Dana syndrome, vitamin B12 neuropathy. (05 Mar 2000) |
| Graves' optic neuropathy | Visual dysfunction due to optic nerve compression in Graves' orbitopathy. (05 Mar 2000) |
| peripheral neuropathy | <neurology> Injury to the nerves that supply sensation to the arms and legs. Origin: Gr. Pathos = disease (16 Dec 1997) |
| chronic interstitial hypertrophic neuropathy | dejerine-Sottas disease |
| motor dapsone neuropathy | A peripheral neuropathy due to ingestion of 4,4-deaminodiphenylsulphone. (05 Mar 2000) |
| compression neuropathy | A focal nerve lesion produced when sustained pressure is applied to a localised portion of the nerve, either from an external or internal source; the main source of injury is the pressure differential that exists between one portion of the nerve and another. (05 Mar 2000) |
| heavy metal neuropathy | Peripheral nervous system disorders attributed to intoxication of one of the heavy metals: arsenic, gold, lead, mercury, platinum and thallium. (05 Mar 2000) |
| hereditary hypertrophic neuropathy | dejerine-Sottas disease |
| hereditary sensory radicular neuropathy | Neuropathy characterised by the occurrence of severe, relapsing foot ulcerations of neuropathic origin, destruction of terminal digits of feet and hands, and a loss of sensation; autosomal dominant inheritance is associated with onset in the second decade or later. (05 Mar 2000) |
| hypertrophic interstitial neuropathy | Sensorimotor neuropathy characterised pathologically by collections of Schwann cell processes arranged concentrically around one or more nerve fibres. No genetic factors are known in its aetiology.For hereditary types, see hereditary hypertrophic neuropathy. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|