Paraneoplastic neuromyopathy and neuropathy (Q85106): Difference between revisions

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As síndromes neurológicas paraneoplásicas (SNP) podem ser definidas como efeitos remotos do câncer que não são causados pelo tumor e suas metástases, ou por infecção, isquemia ou distúrbios metabólicos. Apenas a síndrome miastênica de Lambert-Eaton é relativamente frequente. As outros SNP mais comuns são ataxia cerebelar subaguda, encefalite límbica, Opsoclonus-mioclonus, retinopatias (retinopatia associada ao câncer e retinopatia associada ao melanoma, síndrome da pessoa rígida, pseudoobstrução gastrointestinal crônica, neuronopatia sensorial, encefalomielite e dermatomielite.
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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.

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.
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    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.

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