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Get Free AccessA 10-year-old girl presented with subacute lower limb weakness and gait ataxia. MRI revealed a large multicystic spinal cord lesion with patchy enhancement (figure 1, A and B) and 3 small (<6 mm) periventricular and deep white matter brain lesions. The presence of serum anti-aquaporin-4 (AQP4) immunoglobulin G (ELISA assay) and compatible neuropathologic features from neurosurgical specimens1 (figure 2) suggested the diagnosis of a neuromyelitis optica spectrum disorder.2 Targeted immunotherapy was started, with partial lesion resolution (figure 1C).
Giulia Longoni, Sandra Bigi, Helen M. Branson, Cynthia Hawkins, James T. Rutka, Massimo Filippi, E. Ann Yeh (2014). Multicystic demyelinating myelopathy. , 82(10), DOI: https://doi.org/10.1212/wnl.0000000000000192.
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Type
Article
Year
2014
Authors
7
Datasets
0
Total Files
0
Language
en
DOI
https://doi.org/10.1212/wnl.0000000000000192
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