Movement disorders due to primary central nervous system lymphoma: An illustrative case and systematic literature review.
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TL;DR
The objective of this study was to explore movement disorders in PCNSL and discuss the potential pathophysiological relationships between PCNSL and symptoms and to enable prompt initiation of urgent treatments.
OpenAlex 토픽 ·
CNS Lymphoma Diagnosis and Treatment
Neurological and metabolic disorders
Autoimmune Neurological Disorders and Treatments
The objective of this study was to explore movement disorders in PCNSL and discuss the potential pathophysiological relationships between PCNSL and symptoms and to enable prompt initiation of urgent t
- 연구 설계 systematic review
APA
V. Harlay, V. Mira, et al. (2026). Movement disorders due to primary central nervous system lymphoma: An illustrative case and systematic literature review.. Revue neurologique, 182(4), 248-258. https://doi.org/10.1016/j.neurol.2026.02.152
MLA
V. Harlay, et al.. "Movement disorders due to primary central nervous system lymphoma: An illustrative case and systematic literature review.." Revue neurologique, vol. 182, no. 4, 2026, pp. 248-258.
PMID
41781302 ↗
Abstract 한글 요약
[INTRODUCTION] Movement disorders (MD) can result from various mechanisms: central nervous system infection (20%), trauma (15%), metabolic dysregulation (7%), vascular causes (22%), or inflammatory, degenerative, and tumoral diseases. MD leading to the diagnosis of primary central nervous system lymphoma (PCNSL) are rare but may be treatable, depending on how quickly the diagnosis is made. The objective of this study was to explore movement disorders in PCNSL and discuss the potential pathophysiological relationships between PCNSL and symptoms.
[METHODS] We conducted a systematic review from databases inception (PubMed/MEDLINE and Google Scholar) through July 2025.
[RESULTS] Forty-five cases were found in the literature. An additional case from our records was included, with detailed clinical and paraclinical examinations for illustrative purposes (a 77-year-old man who experienced subacute left hemichorea-hemiballism movements, leading to the discovery of a right-sided lesion involving deep brain structures). Globally, the main movement disorders included gait impairment/ataxia (48%), parkinsonism (20%), chorea/ballism (14%), and tremor (10%). The mean age at onset was 59 years (ranging from 24 to 81), and the sex ratio was 23 males to 23 females.
[CONCLUSION] PCNSL may present with unusual symptoms like movement disorders (which may be of various types). Early diagnosis could enable prompt initiation of urgent treatments.
[METHODS] We conducted a systematic review from databases inception (PubMed/MEDLINE and Google Scholar) through July 2025.
[RESULTS] Forty-five cases were found in the literature. An additional case from our records was included, with detailed clinical and paraclinical examinations for illustrative purposes (a 77-year-old man who experienced subacute left hemichorea-hemiballism movements, leading to the discovery of a right-sided lesion involving deep brain structures). Globally, the main movement disorders included gait impairment/ataxia (48%), parkinsonism (20%), chorea/ballism (14%), and tremor (10%). The mean age at onset was 59 years (ranging from 24 to 81), and the sex ratio was 23 males to 23 females.
[CONCLUSION] PCNSL may present with unusual symptoms like movement disorders (which may be of various types). Early diagnosis could enable prompt initiation of urgent treatments.
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