Your browser doesn't support javascript.
loading
A Case of Neuromyelitis Optica Spectrum Disorder with Visual Hallucination-induced Severe Delirium / 日本プライマリ・ケア連合学会誌
An Official Journal of the Japan Primary Care Association ; : 85-88, 2021.
Article in Japanese | WPRIM | ID: wpr-886195
ABSTRACT

Objective:

Neuromyelitis optica spectrum disorder (NMOSD) is an inflammatory disease of the central nervous system characterized by optic neuritis and myelitis. NMOSD is more prevalent in the elderly than multiple sclerosis. In particular, optic neuritis of NMOSD is common in the elderly.Methods and

Results:

We report an 82-year-old female patient with no medical history who presented with optic neuritis as the first attack of NMOSD. On day X−15, she developed horizontal hemianopia and was referred to our department. On admission, her visual acuity was hand motion. Cerebrospinal fluid suggested pleocytosis. Magnetic resonance imaging revealed a hyper-intense lesion on the optic chiasm and optic tract. Steroid pulse therapy was performed, but from the night, delirium with visual hallucinations developed. She refused drug administration, removed the intravenous administration route, and was unable to continue in-hospital treatment.

Conclusion:

NMOSD often develops in the elderly with optic neuritis, and in addition to steroid therapy, plasma exchange or immunoglobulin therapy is expected to improve the prognosis. However, in our case, treatment was discontinued due to marked delirium accompanied by visual hallucinations. Visual hallucinations are more likely to occur in elderly patients with visual impairment, and clinicians should be careful and manage hallucination-associated delirium.

Search on Google
Index: WPRIM (Western Pacific) Language: Japanese Journal: An Official Journal of the Japan Primary Care Association Year: 2021 Type: Article

Similar

MEDLINE

...
LILACS

LIS

Search on Google
Index: WPRIM (Western Pacific) Language: Japanese Journal: An Official Journal of the Japan Primary Care Association Year: 2021 Type: Article