Progressive supranuclear palsy. description of the clinical case
https://doi.org/10.52485/19986173_2023_1_182
Abstract
Progressive supranuclear palsy (PNP) (progressive supranuclear ophthalmoplegia, progressive supranuclear gaze paresis, Steele-Richardson-Olszewski disease) is a progressive neurodegenerative disease of the central nervous system that belongs to the group of taupathies. Taupathies are a group of diseases characterized by deposits of the tau protein in neurons and glial cells, which subsequently leads to their death. There are several isoforms of the tau protein, on the basis of which a classification of taupathies has been developed: there are 3R-taupathies (Pick's disease), and 4R-taupathies (PNP, corticobasal degeneration, etc.), there are also "mixed" taupathies (Alzheimer's disease). The article describes a rare variant of the course of PNP with corticobasal syndrome. The course of this disease was accompanied by polymorphic neurological symptoms in the form of various motor disorders, oculomotor disorders, disorders of the emotional-volitional sphere.
Keywords
About the Authors
A. Yu. Ma-Van-deRussian Federation
672090; 39 A Gorkogo str.; Chita
Yu. A. Shirshov
Russian Federation
672090; 39 A Gorkogo str.; Chita
F. Yu. Belozertsev
Russian Federation
672090; 39 A Gorkogo str.; Chita
References
1. Steele JC., Richardson JC., Olszewski J. Progressive supranuclear palsy. A heterogeneous degeneration involving the brain stem, basal ganglia and cerebellum with vertical gaze and pseudobulbar palsy, nuchal dystonia and dementia. Arch. Neurol. 1964. 10. 333–359.
2. Takigawa H., et al. Prevalence of progressive supranuclear palsy in Yonago: change throughout a decade. Brain, Behavior, and Immunity. 2016. 6 (12).
3. Younes K., Miller BL. Frontotemporal Dementia: Neuropathology, Genetics, Neuroimaging, and Treatments. Psychiatric Clinics of North America. 2020. 4(2). 331-344.
4. Murley A.G., Coyle-Gilchrist I., Rouse M.A. Redefining the multidimensional clinical phenotypes of frontotemporal lobar degeneration syndromes. Brain. 2020. 143. 1555–1571.
5. McFarland N.R. Diagnostic approach to atypical parkinsonian syndromes. Continuum (Minneap. Minn.). Movement Disorders. 2016. 22 (4). 1117-1142.
6. Tappakhov A.A., Popova T.E., Govorova T.G., Petrova A.Yu. Clinical heterogeneity of progressive supranuclear palsy. Annals of clinical and experimental neurology. 2018. 12(2). 33-38. in Russian.
7. Magzhanov R.V., Davletova A.I., Ibatullin R.A., Tunik V.F., Idrisova R.F., Bakhtiyarova K.Z. Difficulties in the differential diagnosis of progressive supranuclear palsy and Parkinson's disease. Annals of clinical and experimental neurology. 2016. 10(4). 58-61. in Russian.
8. Valikova T.A., Alifirova V.M., Pugachenko N.V., Tsyrenzhapova R.B., Bichik A.B. Clinical features of supranuclear palsy. Bulletin of Siberian medicine. 2009. 8(3-2). 78-82. in Russian.
9. Sanches C., Stengel C., Godard J., et al. Past, Present, and Future of Non-invasive Brain Stimulation Approaches to Treat Cognitive Impairment in Neurodegenerative Diseases: Time for a Comprehensive Critical Review. Front Aging Neurosci. 2021. 20(1). 12:578339.
10. Litvan I., Agid Y., Calne D., et al. Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop. Neurology. 1996. 47(1). 1-9.
11. Höglinger G.U., Respondek G., Stamelou M., et al. Clinical diagnosis of progressive supranuclear palsy: the movement disorder Society criteria. Movement Disorders. 2017. 32 (6). 853–864.
12. Boxer A.L., Yu J.T., Golbe L.I., et al. Advances in progressive supranuclear palsy: new diagnostic criteria, biomarkers, and therapeutic approaches. Lancet Neurology. 2017. 16 (7). 552-563.
13. Aludin S., Schmill L.A. MRI Signs of Parkinson's Disease and Atypical Parkinsonism. Rofo. 2021. 193(12). 1403-1410.
Review
For citations:
Ma-Van-de A.Yu., Shirshov Yu.A., Belozertsev F.Yu. Progressive supranuclear palsy. description of the clinical case. Transbaikalian Medical Bulletin. 2023;(1):182-187. (In Russ.) https://doi.org/10.52485/19986173_2023_1_182