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Abstract Details

Case Series: Two Cases of First Presentation AQP4-IgG Antibody Positive Neuromyelitis Optica in Patients of Advanced Age as a Possible Paraneoplastic Phenomenon
Autoimmune Neurology
Autoimmune Neurology Posters (7:00 AM-5:00 PM)
108
We describe 2 cases with positive AQP4-IgG antibodies and tumors. An 83-year-old male presented with bilateral, sequential optic neuritis and simultaneous longitudinally extensive transverse myelitis; a papillary thyroid carcinoma was identified subsequently. A 75-year-old male with known mesothelioma presented with severe longitudinally extensive transverse myelitis and subsequent relapse with unilateral optic neuritis.

Aquaporin-4 (AQP4) positive neuromyelitis optica is increasingly recognized in diverse age groups. With advanced age, a possible paraneoplastic association needs consideration.

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Case 1:

An 83-year-old male presented for evaluation of progressive loss of left eye vision over 48 hours. 3 weeks prior there was abrupt onset of loss of right eye vision. Over the same time period there was lower limb sensory loss and weakness.

Magnetic resonance imaging identified increased pre-chiasmal right optic nerve T2 signal and bilateral optic atrophy. Spinal imaging revealed a longitudinally extensive T3-T6 cord T2 hyperintensity.

Cerebrospinal fluid constituents were unremarkable. Serum and CSF anti-AQP4 antibodies were positive on rodent tissue and fixed transfected cell lines. Papillary thyroid carcinoma was identified during malignancy screening.

 

Case 2:

A 75-year old male with mesothelioma presented with lower limb paraparesis, bladder and bowel dysfunction, and a thoracic sensory level.

Magnetic resonance imaging identified longitudinally extensive T2 spinal cord hyperintensity from C3/4 to T11/12 with cord expansion.

Cerebrospinal fluid analysis demonstrated a lymphocytic pleocytosis with elevated protein. Serum anti-AQP4 antibodies were positive on rodent tissue and fixed transfected cell lines.

One year after treatment with Rituximab, a relapse with left optic neuritis occurred in the context of B-cell recovery.

A high index of suspicion for neuromyelitis optica is required in all age groups with an appropriate clinical presentation. A paraneoplastic association may exist in older age groups. Simultaneous optic neuritis and transverse myelitis can occur in the context of AQP4 antibodies in older populations.
Authors/Disclosures
Reuben Beer, MBBS
PRESENTER
Dr. Beer has nothing to disclose.
No disclosure on file
Helen G. Brown, MD (The Royal Brisbane and Women's Hospital) Dr. Brown has nothing to disclose.
Stefan Blum, PhD, FRACP (Princess Alexandra Hospital) The institution of Dr. Blum has received research support from Merck. The institution of Dr. Blum has received research support from MSRA. The institution of Dr. Blum has received research support from PA Research Foundation.