Publications by authors named "Yuwa Oka"

Hemodialysis is a well-known risk factor for severe infection by putting patients under an immunocompromised state. Such patients are prone to opportunistic pathogen and present with atypical manifestations during infection. Tuberculous meningitis is a central nervous system infection of Mycobacterium tuberculosis, accounting for the highest mortality of all forms of tuberculosis.

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A 60-year-old man with a history of bronchial asthma and nasal polyp presented with loss of vision in the right eye. His visual loss progressed within a single day, and he presented to our hospital 5 days after the onset of the symptom. Fundoscopy showed swelling and hemorrhage of the right optic disc.

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Article Synopsis
  • This study investigates the nerve ultrasonographic features of IgM/anti-MAG neuropathy in a Japanese population, aiming to see how they compare with common subtypes of chronic inflammatory demyelinating polyneuropathy (CIDP).
  • Researchers analyzed the cross-sectional areas of cervical nerve roots and peripheral nerves in patients with IgM/anti-MAG neuropathy, typical CIDP (t-CIDP), multifocal CIDP (m-CIDP), and healthy controls.
  • Findings show that while IgM/anti-MAG neuropathy has larger nerve cross-sectional areas similar to t-CIDP, they show greater enlargement at common entrapment sites compared to t-CIDP, highlighting the need for further cross-pop
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We herein report a 49-year-old man with a fever, diagnosed with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. After two weeks of hospitalization, he suddenly mentioned visual field impairment. Computed tomography and magnetic resonance imaging revealed white matter damage and vasogenic edema.

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Background: Multifocal motor neuropathy (MMN) occasionally presents with cranial nerve involvement. However, no MMN cases with visual pathway impairment demonstrated by visual evoked potential (VEP) have been reported.

Case Report: A 36-year-old man was admitted to our hospital with progressive muscular weakness.

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Multifocal enlargements with the alteration of a normal fascicular pattern are considered to be sonographic peripheral nerve features in multifocal acquired demyelinating sensory and motor neuropathy (MADSAM), a subtype of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). We herein present the case of an 18-year-old patient with MADSAM in whom intensive sonological assessments revealed multifocal nerve enlargement within clinically affected cranial nerves. Our case demonstrated that, if systematically investigated with ultrasound, morphological changes similar to those in the peripheral nerves may be detected in a large proportion of clinically affected cranial nerves in MADSAM, boosting the future applications of cranial nerve ultrasound in CIDP.

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Background: Mutations in the tau gene linked to chromosome 17 cause frontotemporal dementia and parkinsonism (FTDP-17).

Objective: This study presents 3 Japanese familial cases diagnosed with N279K tau gene mutation, including 1 autopsy-confirmed case.

Methods: We compared the clinical presentations, cognitive functions, and images between the 3 familial cases diagnosed with N279K mutation.

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Cerebral air embolism (CAE) is a rare but well-known complication resulting from invasive medical procedures; however, previous studies have not examined the postoperative longitudinal MRI changes in CAE. In particular, the likelihood that such changes may be observed after an initial delay when using magnetic resonance imaging (MRI) has not been explored. We herein report a case of CAE with no MRI abnormalities 4 h after a pulmonary vein isolation (PVI) procedure and where the first abnormality was found 22 h after the procedure.

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Visual impairment can occur because of several mechanisms, including optic nerve disease and occasionally fungal sinusitis. An 87-year-old man presented with the loss of right visual acuity; he was diagnosed with optic neuritis. Steroid pulse therapy was not effective.

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Article Synopsis
  • Cavernous sinus dural arteriovenous fistula symptoms can vary widely, with brainstem dysfunction being a rare and serious outcome.
  • In an 80-year-old woman, symptoms quickly progressed from gait disturbance to confusion, dysarthria, and left hemiparesis, leading to a coma within days.
  • Unlike other cases where ocular symptoms appeared first, this case exhibited only brainstem symptoms, complicating diagnosis, highlighting the need for swift imaging and treatment to prevent long-term damage.
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