Paraneoplastic neurological syndromes (PNS) are immune-mediated neurological disorders that can affect any part of the nervous system, occur in association with cancer and are often supported by the presence of specific neuronal autoantibodies.
Neuronal autoantibodies are classified as high-, intermediate-, or low-risk for paraneoplastic aetiology. High-risk antibodies have a >70% cancer association, recognise intracellular antigens and are not directly pathogenic. The tumour type depends on patient demographics and on the specific neuronal autoantibody identified.
Anti-Yo (CDR2 or PCA-1) antibodies are markers of autoimmune neuronal disease such as rapidly progressive cerebellar syndrome. Their association with breast and ovarian cancer is >90%.
For high-risk PNS, autoantibody testing should be performed using at least two independent methods.
Serum, EDTA plasma, heparin plasma, citrate plasma, CSF
Immunoblot, IFA cells,
Fasting for at least 8-12 hours before sampling
Refer to the Health Service Charter to check storage conditions
+2/+8°C
This test provides the quantitative determination of total tau protein to support the diagnosis of Alzheimer’s disease.
This test provides the quantitative determination of tau protein phosphorylated at threonine 181 (pTau181), to support the diagnosis of Alzheimer’s disease.
Test for the determination of human autoantibodies against NMDAR to support the diagnosis of paraneoplastic neurological syndromes with an intermediate-risk phenotype.
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