| 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) |
|---|
| paracarcinomatous myelopathy | Degeneration or necrosis of the spinal cord associated with a carcinoma. Synonym: paracarcinomatous myelopathy. (05 Mar 2000) |
|---|---|
| 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) |
| 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) |
| 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) |