Evidence map›Paper›PMID 42564694›Full record

ArticleRadiology case reports2026

Neuromyelitis optica presenting with mammillary body and cervicomedullary lesions after severe hyponatremia mimicking osmotic demyelination syndrome.

Madison S Meyer, Keyanna Lewis, Mohamad Ahmed, Shoshanah Lasry, Cameron Peres, Fred Ahmadi, Adam Khanafer

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Article in Radiology case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Madison S MeyerDepartment of Medicine, Wayne State University School of Medicine, 540 E Canfield St, Detroit, MI 48201, USA.
Keyanna LewisDepartment of Medicine, American University of the Caribbean School of Medicine, Cupecoy, Sint Maarten.
Mohamad AhmedDepartment of Medicine, Ross University School of Medicine, Saint Michael, Barbados.
Shoshanah LasryDepartment of Medicine, Dr. Kiran C. Patel College of Osteopathic Medicine, Nova Southeastern University, 3200 S University Dr, Fort Lauderdale, FL 33328, USA.
Cameron PeresDepartment of Internal Medicine, Providence Henry Ford, 16001 W Nine Mile Rd, Southfield, MI 48075, USA.
Fred AhmadiDepartment of Internal Medicine, Providence Henry Ford, 16001 W Nine Mile Rd, Southfield, MI 48075, USA.
Adam KhanaferDepartment of Psychiatry, Providence Henry Ford, 16001 W Nine Mile Rd, Southfield, MI 48075, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuromyelitis optica spectrum disorder is an autoimmune demyelinating disease that usually targets the spinal cord and optic nerves, though occasionally other central nervous system structures are involved. There are variants of neuromyelitis optica spectrum disorder that can mimic metabolic or osmotic demyelinating diseases on imaging. A 54-year-old female with a history of hypertension and Roux-en-Y bypass presented with numbness, weakness, dizziness, and blurred vision and concurrent severe hyponatremia (serum sodium 115 mmol/L). She was admitted and treated for monitored correction of her symptomatic hyponatremia and was discharged after stabilization. Weeks following discharge, she had onset of new neurological symptoms and brain magnetic resonance imaging revealed increased fluid-attenuated inversion recovery signal in the bilateral mammillary bodies and dorsal columns of the upper cervical spinal cord, patchy enhancement at the cervicomedullary junction, and a lesion at C2-C3. Cerebrospinal fluid studies were unremarkable. While osmotic demyelination was suspected initially based on the history of profound hyponatremia and distribution of lesions, further neurologic assessment confirmed neuromyelitis optica spectrum disorder. To our knowledge, only 1 other case of mammillary body involvement in AQP4-positive neuromyelitis optica spectrum disorder presenting in the setting of severe hyponatremia and with close radiographic resemblance to osmotic demyelination syndrome has been reported. In summary, our case demonstrates radiographic mimicry of osmotic demyelination syndrome by neuromyelitis optica spectrum disorder. Consideration of neuromyelitis optica spectrum disorder should be maintained on the differential diagnosis of patients with mammillary body and cervicomedullary lesions following hyponatremia, especially with regard to the presence of enhancement and progression of lesions.

Indexed as

Cervicomedullary junctionExtrapontine myelinolysisHyponatremiaInflammatory myelopathyNeuromyelitis optica spectrum disorderOsmotic demyelination syndrome

Identifiers

PMID42564694
PMCPMC13444491

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