| INE | infantile necrotizing encephalomyelopathy |
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| PCD | pacer-cardioverter-defibrillator; papillary collecting duct; paraneoplastic cerebellar degeneration;... |
| PLE | paraneoplastic limbic encephalopathy; protein-losing enteropathy; pseudolupus erythematosus |
| PNEM | paraneoplastic encephalomyelitis |
| PNS | paraneoplastic syndrome; parasympathetic nervous system; partial nonprogressive stroke; peripheral n... |
| SNE | Subacute necrotizing encephalomyelopathy |
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| PCD | Paraneoplastic cerebellar degeneration |
| PEM | Paraneoplastic encephalomyelitis |
| PNP | Paraneoplastic pemphigus |
| paraneoplastic encephalomyelopathy | An encephalomyelopathy as a remote effect of carcinoma, most often oat cell carcinoma of the lung; characterised by extensive nerve cell loss, which may be diffuse, but often predominates in particular portions of the central nervous system, particularly the limbic lobes, medulla, cerebellum, and gray matter of the spinal cord. Synonym: carcinomatous encephalomyelopathy, encephalomyelitis associated with carcinoma, paracarcinomatous encephalomyelopathy. (05 Mar 2000) |
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| paraneoplastic | Relating to or characteristic of paraneoplasia. (05 Mar 2000) |
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| paraneoplastic acrokeratosis | <syndrome> Erythematous to plum-coloured scaly acral skin lesions, paronychia, and nail dysplasia; associated with cancer of the upper respiratory or upper alimentary tract. Synonym: paraneoplastic acrokeratosis. (05 Mar 2000) |
| paraneoplastic syndrome | <oncology, syndrome> A collection of symptoms or clinical signs that are found in patients that have malignant disease. By definition, the signs and symptoms are not produced by a direct effect of a tumour or its metastasis nor due to direct invasion, compression, metastasis, infection, nutritional deficiency or treatment of the underlying neoplasm. Paraneoplastic syndromes can arise from tumour produced biologically active polypeptides or proteins, autoimmunity or immune complex production and immune suppression, blockade of the normal effect of a hormone, the release of substances from tumour associated endothelium which are not normally released and finally unknown causes. The best characterised paraneoplastic syndrome is the syndrome of inappropriate ADH. (15 Dec 1997) |
| paraneoplastic syndromes | In patients with neoplastic diseases a wide variety of clinical pictures which are indirect and usually remote effects produced by tumour cell metabolites or other products. (12 Dec 1998) |
| carcinomatous encephalomyelopathy | An encephalomyelopathy as a remote effect of carcinoma, most often oat cell carcinoma of the lung; characterised by extensive nerve cell loss, which may be diffuse, but often predominates in particular portions of the central nervous system, particularly the limbic lobes, medulla, cerebellum, and gray matter of the spinal cord. Synonym: carcinomatous encephalomyelopathy, encephalomyelitis associated with carcinoma, paracarcinomatous encephalomyelopathy. (05 Mar 2000) |
| paracarcinomatous encephalomyelopathy | An encephalomyelopathy as a remote effect of carcinoma, most often oat cell carcinoma of the lung; characterised by extensive nerve cell loss, which may be diffuse, but often predominates in particular portions of the central nervous system, particularly the limbic lobes, medulla, cerebellum, and gray matter of the spinal cord. Synonym: carcinomatous encephalomyelopathy, encephalomyelitis associated with carcinoma, paracarcinomatous encephalomyelopathy. (05 Mar 2000) |
| necrotizing encephalomyelopathy | Subacute encephalomyelopathy affecting infants, causing dementia, spasticity, and optic atrophy; autosomal recessive inheritance. Synonym: necrotizing encephalomyelopathy, necrotizing encephalopathy. (05 Mar 2000) |
| subacute necrotizing encephalomyelopathy | A rare fatal disorder, primarily of children, being both acute and chronic in onset, manifested primarily as brainstem dysfunction, with ataxia, cranial nerve palsies, pseudobulbar palsy, hemi-or quadriplegia, mental deterioration, and involuntary movements; deficiencies of pyruvate dehydrogenase or cytochrome C oxydase have been found in some patients; pathologically, there is widespread symmetric necrosis involving much of the brainstem; these changes are similar to those seen with Wernicke encephalopathy. (05 Mar 2000) |
| encephalomyelopathy | Any disease of both brain and spinal cord. Origin: G. Enkephalos, brain, + myelon, marrow, + pathos, suffering (05 Mar 2000) |
| epidemic myalgic encephalomyelopathy | A disease superficially resembling poliomyelitis, characterised by diffuse involvement of the nervous system associated with myalgia. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|