Case report: Saccadic ping-pong gaze in progressive supranuclear palsy with predominant postural instability.

case report macro square wave jerks ping-pong gaze postural instability progressive supranuclear palsy saccadic ping-pong gaze the movement disorder society criteria transitory alternating saccades

Journal

Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899

Informations de publication

Date de publication:
2023
Historique:
received: 17 11 2022
accepted: 06 02 2023
entrez: 20 3 2023
pubmed: 21 3 2023
medline: 21 3 2023
Statut: epublish

Résumé

We report a 63-year-old female patient with progressive supranuclear palsy (PSP). She presented predominant postural instability and "saccadic ping-pong gaze" (SPPG). She had unprovoked falls recurrently within a year from the onset of gait disturbance. She tended to fall backward with eye closure but had no freezing of gait on examination. She showed no signs of nuchal dystonia, limb tremor, rigidity, spasticity, or ataxia. The dopaminergic response was negative. On the initial examination, her vertical eye movements were normal, but frequent macro square wave jerks and SPPG were observed. SPPG consisted of short-cycle, horizontal conjugate irregular pendular oscillations of the eye position from the midpoint with superimposed small saccades. SPPG was observed usually in the dark, not in the daylight, and with eye closure by using electrooculogram and infrared charge-coupled device imaging. One and a half years after the first examination, she was diagnosed as probable PSP with vertical supranuclear gaze palsy. SPPG was first described in patients who are unconscious by Johkura in 1998 as a "saccadic" variant of "ping-pong gaze (PPG)." PPG, short-cycle periodic alternating gaze, has been described in comatose patients since 1967. On the other hand, abnormal eye movement, which looks the same as SPPG in coma, has been described in conscious patients with PSP or spinocerebellar degeneration (SCD) in Japanese literature since 1975. However, it has been called "transient alternating saccades (TAS)." Nowadays, we believe it is more appropriate to call this abnormal eye movement "SPPG" instead of TAS. Here, we propose that PSP, a neuro-degenerative disease, should be added as one of the etiologies of SPPG. We discuss the differences between PPG/SPPG in coma and SPPG in PSP and the possible pathophysiological mechanism of SPPG in relation to cerebellar oculomotor dysfunctions.

Identifiants

pubmed: 36937509
doi: 10.3389/fneur.2023.1100931
pmc: PMC10014735
doi:

Types de publication

Case Reports

Langues

eng

Pagination

1100931

Informations de copyright

Copyright © 2023 Nunomura, Kasahara, Hatano, Shimada, Takado, Endo, Inoshita, Inomata, Murofushi, Misawa, Machida and Imai.

Déclaration de conflit d'intérêts

The co-publisher of QST, HS, is the inventor of the patent for the tau PET imaging agent. HS holds a patent on compounds related to the present report (JP 5422782/EP12 884 742.3/CA2894994/HK1208672). QST has a license agreement with APRINOIA Therapeutics Inc., for the above patent. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

Radiology. 2008 Jan;246(1):214-21
pubmed: 17991785
Arch Neurol. 1964 Apr;10:333-59
pubmed: 14107684
Neurologist. 2007 May;13(3):161-3
pubmed: 17495763
Acta Neuropathol Commun. 2016 Nov 14;4(1):120
pubmed: 27842578
Neurology. 1993 Jun;43(6):1067-70
pubmed: 8170542
J Neurosci. 2011 Mar 23;31(12):4379-87
pubmed: 21430139
Lancet Neurol. 2011 Aug;10(8):734-44
pubmed: 21777828
Exp Brain Res. 2014 Jan;232(1):191-210
pubmed: 24129645
Mov Disord. 2017 Jun;32(6):853-864
pubmed: 28467028
Neurology. 1976 Jun;26(6 PT 1):532-5
pubmed: 945493
Ann Neurol. 1984 May;15(5):465-73
pubmed: 6732193
J Neurol Neurosurg Psychiatry. 1967 Oct;30(5):383-92
pubmed: 6062990
Brain. 2008 Apr;131(Pt 4):1035-45
pubmed: 18238798
Mov Disord. 2014 Apr;29(4):488-95
pubmed: 24573655
No To Shinkei. 1989 Feb;41(2):125-32
pubmed: 2736143
J Neuroophthalmol. 1998 Mar;18(1):43-6
pubmed: 9532540

Auteurs

Hikari Nunomura (H)

Department of Neurology, Tokyo Rinkai Hospital, Tokyo, Japan.

Taketoshi Kasahara (T)

Division of Rehabilitation, Tokyo Rinkai Hospital, Tokyo, Japan.

Taku Hatano (T)

Department of Neurology, School of Medicine, Juntendo University, Tokyo, Japan.

Hitoshi Shimada (H)

Department of Functional Neurology & Neurosurgery, Center for Integrated Human Brain Science, Niigata University, Niigata, Japan.
Department of Functional Brain Imaging Research, Institute for Quantum Medical Science, Quantum Life and Medical Science Directorate, National Institutes for Quantum Science and Technology (QST), Chiba, Japan.

Yuhei Takado (Y)

Department of Functional Brain Imaging Research, Institute for Quantum Medical Science, Quantum Life and Medical Science Directorate, National Institutes for Quantum Science and Technology (QST), Chiba, Japan.

Hironobu Endo (H)

Department of Functional Brain Imaging Research, Institute for Quantum Medical Science, Quantum Life and Medical Science Directorate, National Institutes for Quantum Science and Technology (QST), Chiba, Japan.

Ayako Inoshita (A)

Department of Otorhinolaryngology, School of Medicine, Juntendo University, Tokyo, Japan.

Atsuko Inomata (A)

Department of Otorhinolaryngology, School of Medicine, Juntendo University, Tokyo, Japan.

Toshihisa Murofushi (T)

Department of Otorhinolaryngology, Mizonokuchi Hospital, Teikyo University, Kawasaki, Japan.

Shihoko Misawa (S)

Department of Neurology, Tokyo Rinkai Hospital, Tokyo, Japan.

Yutaka Machida (Y)

Department of Neurology, Tokyo Rinkai Hospital, Tokyo, Japan.

Hisamasa Imai (H)

Department of Neurology, Tokyo Rinkai Hospital, Tokyo, Japan.

Classifications MeSH