Misleading Medulla: Atypical NMOSD Masquerading as Posterior Circulation Stroke

Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune astrocytopathy which typically involve the optic nerves, spinal cord and brain stem regions. It?s an Aquaporin - 4 related channelopathy. Typically characterized by the core clinical features of optic neuritis, acute myelitis, area postrema syndrome, acute diencephalic syndrome, acute brainstem syndrome and symptomatic cerebral syndrome. Although clinical presentation of the patients can be variable. Herein we report an interesting case of 33 - year young female patient who initially presented with acute onset ataxia and vertigo, her imaging was suggestive of right lateral medullary infarct. Therefore, she was started on antiplatelets and statin. However, patient clinically worsened along with new symptoms. On further evaluation, patient serum serology was strongly positive for Aquaporin - 4 antibody thus turning out to be NMOSD. Subsequently our patient revealed that her maternal aunt also diagnosed with NMOSD four years back, suggesting likely a familial predisposition.

Authors

Publication Details

Journal
International Journal of Science and Research (IJSR)
Published
2025-06-06
DOI
https://doi.org/10.21275/mr25526222911
Primary Topic
Tuberous Sclerosis Complex Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Misleading Medulla: Atypical NMOSD Masquerading as Posterior Circulation Stroke

Deepika Dalal, Mridula Singh, Ritesh Kumar, Rajinder K Dhamija
International Journal of Science and Research (IJSR)
Tuberous Sclerosis Complex Research
article

Misleading Medulla: Atypical NMOSD Masquerading as Posterior Circulation Stroke

Deepika Dalal, Mridula Singh, Ritesh Kumar, Rajinder K Dhamija
article en

Abstract

Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune astrocytopathy which typically involve the optic nerves, spinal cord and brain stem regions. It?s an Aquaporin - 4 related channelopathy. Typically characterized by the core clinical features of optic neuritis, acute myelitis, area postrema syndrome, acute diencephalic syndrome, acute brainstem syndrome and symptomatic cerebral syndrome. Although clinical presentation of the patients can be variable. Herein we report an interesting case of 33 - year young female patient who initially presented with acute onset ataxia and vertigo, her imaging was suggestive of right lateral medullary infarct. Therefore, she was started on antiplatelets and statin. However, patient clinically worsened along with new symptoms. On further evaluation, patient serum serology was strongly positive for Aquaporin - 4 antibody thus turning out to be NMOSD. Subsequently our patient revealed that her maternal aunt also diagnosed with NMOSD four years back, suggesting likely a familial predisposition.

International Journal of Science and Research (IJSR)
Gender equality
Openalex Percentile: Top 83%
Tuberous Sclerosis Complex Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.