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Evaluation of an Exclusive Spur Dike U-Turn Design with Radar-Collected Data and Simulation
Published on: February 1, 2020
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At this junction….
Alexander M Warwick1, Sidney M Gospe1, John J Chen2
1Department of Ophthalmology, Duke University Medical Center, Durham NC, USA.
Survey of Ophthalmology
|August 8, 2021
Summary
An elderly woman experienced painful vision loss, diagnosed as aquaporin-4 positive neuromyelitis optic spectrum disorder. Prompt therapeutic plasma exchange significantly improved her vision, highlighting its efficacy in optic neuritis management.
Area of Science:
- Neuro-ophthalmology
- Autoimmune Neurology
Background:
- Neuromyelitis optic spectrum disorder (NMOSD) is a rare autoimmune condition affecting the optic nerves and spinal cord.
- Optic neuritis is a common initial presentation of NMOSD, often leading to significant vision impairment.
Observation:
- An 81-year-old woman presented with acute, painful vision loss in her right eye.
- Ophthalmic examination revealed no acute pathology, but visual field testing indicated a superotemporal defect in the left eye.
- MRI revealed enhancement of the right optic nerve extending to the optic chiasm.
Findings:
- The patient's vision did not improve with intravenous corticosteroids.
- Significant visual recovery was achieved with therapeutic plasma exchange (TPE).
- Serological testing confirmed the presence of aquaporin-4 autoantibodies, establishing the diagnosis of NMOSD.
Implications:
- This case underscores the importance of considering NMOSD in elderly patients presenting with optic neuritis, even without typical spinal cord involvement.
- Therapeutic plasma exchange can be an effective treatment for vision-threatening NMOSD, particularly when corticosteroids fail.
- Early diagnosis and prompt initiation of appropriate treatment, such as TPE, are crucial for visual recovery in NMOSD.
Keywords:
junctional scotomaneuromyelitis optica spectrum disorderoptic neuritisplasma exchangeretrobulbar optic neuropathyMore Related Videos
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