Paraneoplastic neuromyopathy and neuropathy (Q85106): Difference between revisions
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13 August 2026
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Latest revision as of 10:28, 15 August 2026
Paraneoplastic neurological syndromes (PNS) can be defined as remote effects of cancer that are not caused by the tumour and its metastasis, or by infection, ischaemia or metabolic disruptions. Only the Lambert-Eaton myasthenic syndrome is relatively frequent. The other most common PNS are subacute cerebellar ataxia, limbic encephalitis, opsoclonus-myoclonus, retinopathies (cancer-associated retinopathy and melanoma-associated retinopathy, Stiff-Person syndrome, chronic gastrointestinal pseudoobstruction, sensory neuronopathy, encephalomyelitis and dermatomyositis.
| Language | Label | Description | Also known as |
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| default for all languages | ID_711941019 |
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| English | Paraneoplastic neuromyopathy and neuropathy |
Paraneoplastic neurological syndromes (PNS) can be defined as remote effects of cancer that are not caused by the tumour and its metastasis, or by infection, ischaemia or metabolic disruptions. Only the Lambert-Eaton myasthenic syndrome is relatively frequent. The other most common PNS are subacute cerebellar ataxia, limbic encephalitis, opsoclonus-myoclonus, retinopathies (cancer-associated retinopathy and melanoma-associated retinopathy, Stiff-Person syndrome, chronic gastrointestinal pseudoobstruction, sensory neuronopathy, encephalomyelitis and dermatomyositis. |
Statements
CID11:ID_711941019
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dki-india-ID_711941019
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Concluído
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13 August 2026
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