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Egyptian Journal of Radiology and Nuclear Medicine
Fig. 4 | Egyptian Journal of Radiology and Nuclear Medicine

Fig. 4

From: MRI features of myelin oligodendrocyte glycoprotein antibody disease: a descriptive study—how it differs from neuromyelitis optica spectrum disorders and multiple sclerosis

Fig. 4

The case illustrates MOGAD-related encephalitis in a 48-year-old male who presented with generalized tonic–clonic seizures. The brain lesions show typical characteristics of MOGAD—bilateral, asymmetrical, T2 hyperintense, and poorly demarcated with a fluffy appearance. a Axial T2 FLAIR MR image shows hyperintense signal in bilateral basal ganglia, cortex, and subcortical and deep white matter in parieto-temporal lobes. b Axial T2 FLAIR MR image shows hyperintense signal in bilateral cortex and subcortical and deep white matter in fronto-parietal lobes (more on left side). c Axial T2 FLAIR MR image shows hyperintense signal in pons and cerebellum

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