Paraneoplastic neuromyopathy and neuropathy (Q85106): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed an Item
‎Changed an Item
Property / Canary Token
 
dki-india-ID_711941019
Property / Canary Token: dki-india-ID_711941019 / rank
 
Normal rank

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
default for all languages
ID_711941019
    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
      0 references
      dki-india-ID_711941019
      0 references