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Update on neurological paraneoplastic syndromes
Romana Höftberger1, Myrna R Rosenfeld, Josep Dalmau
1aInstitute of Neurology, Medical University of Vienna, Austria bDepartment of Neurology, Hospital Clínic /Institut d'Investigació Biomèdica August Pi i Sunyer (IDIBAPS) cInstitució Catalana de Recerca i Estudis Avançats (ICREA) and Hospital Clínic/ Institut d'Investigació Biomèdica August Pi i Sunyer (IDIBAPS).
Paraneoplastic neurologic syndromes (PNS) present diverse symptoms and can be linked to specific tumors. Early detection and treatment, including immunotherapy, significantly improve patient outcomes.
Area of Science:
- Neurology
- Oncology
- Immunology
Background:
- Paraneoplastic neurologic syndromes (PNS) are a group of disorders triggered by an underlying cancer.
- They can manifest as isolated syndromes (e.g., cerebellar degeneration, limbic encephalitis) or complex phenotypes affecting multiple neurological levels.
Purpose of the Study:
- To provide an updated overview of paraneoplastic neurologic syndromes.
- To discuss associated tumors and the immune responses involved.
- To highlight recent therapeutic advancements.
Main Methods:
- Review of current literature on paraneoplastic neurologic syndromes.
- Analysis of diagnostic approaches, including antibody detection.
- Evaluation of treatment strategies and their efficacy.
Main Results:
- PNS exhibit diverse clinical presentations, from localized to widespread neurological deficits.
- Detection of specific antineuronal antibodies aids in diagnosis and cancer identification.
- Certain antibody-associated PNS demonstrate significant responsiveness to tumor-directed therapies and immunotherapy.
Conclusions:
- Recognizing PNS is crucial for early malignancy detection and timely treatment initiation.
- Prompt therapy offers the best chance to stabilize or improve neurological deficits.
- Syndromes associated with cell surface antibodies often lead to substantial recovery.
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