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Research Article Open access CC BY 4.0

Neuromyelitis Optica Spectrum Disorder Presenting as Cervicothoracic Longitudinally Extensive Transverse Myelitis in a Patient with Advanced Chronic Kidney Disease

Suganthakumari Francis, S. Sowmiya, A. Ishwarya

Asian Journal of Research and Reports in Neurology · pp. 339–352 · Published 1 Aug 2026

10.9734/ajorrin/2026/v9i1189

Abstract

Aims: To present the diagnostic differentiation and multidisciplinary neuro-renal nursing management of a rare, life-threatening presentation of Neuromyelitis Optica Spectrum Disorder (NMOSD) complicated by advanced Stage 4 chronic kidney disease (CKD). Presentation of Case: A 42-year-old female with known Stage 4 CKD presented with a 5-day history of progressive asymmetric quadriparesis, absolute urinary retention, a T4 sensory level, and Class C/D lethargy progressing to respiratory compromise. Spinal magnetic resonance imaging (MRI) revealed a longitudinally extensive transverse myelitis (LETM) lesion spanning C4 to T8. Brain MRI showed periependymal lesions around the third ventricle and area postrema. Serological testing confirmed a strongly positive result for anti-aquaporin-4 antibodies (AQP4-IgG). Laboratory findings confirmed advanced renal failure (serum creatinine: 3.8 mg/dL, blood urea: 82 mg/dL, eGFR: 18 mL/min/1.73m²). The patient was treated with high-dose intravenous methylprednisolone (1 g/day for 5 days) alongside five cycles of therapeutic plasma exchange (PLEX). Comprehensive, targeted neuro-renal nursing interventions addressed airway preservation, fluid restriction, avoidance of systemic risks, and neurogenic bladder care. Following therapy, her sensorium normalised completely, and motor strength improved to 4/5 in all extremities. Discussion: NMOSD should be considered in patients presenting with acute longitudinally extensive transverse myelitis and altered sensorium, particularly when MRI findings and AQP4-IgG serology support the diagnosis. Coexisting advanced CKD may complicate both diagnosis and treatment, requiring individualised management strategies. Conclusion: Early recognition of NMOSD, prompt initiation of immunotherapy, and multidisciplinary neuro-nephrology care can improve neurological outcomes even in critically ill patients with advanced CKD.

Neuromyelitis optica spectrum disorder longitudinally extensive transverse myelitis chronic kidney disease uremic encephalopathy plasma exchange nursing care

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