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. 2024 Oct 30;15(12):387–395. doi: 10.14740/jmc4336

Table 2. Longitudinal Disease Course.

Time point Clinical findings Laboratory data Imaging findings Treatment
Hospital admission (initial presentation) Left face and hemibody paresthesias CSF: mild leukocytosis, 5 CSF-specific oligoclonal bands MRI brain: T2 FLAIR hyperintensity in the bilateral periventricular regions and right pons; cranial nerve enhancement 5-day course of high-dose IV methylprednisolone
Abnormal gait with left leg dragging Serum: positive anti-SSB antibody; no serum oligoclonal bands MRI spine: enhancement in the cauda equina and thoracic nerve roots
Weakness in left hip and knee
Absent lower extremity reflexes
Hospital discharge (8 days post-admission) Mild improvement in strength No new laboratory findings No new imaging findings Discharged with follow-up to neuroimmunology and rheumatology
Persistent left-sided paresthesias
2 months post-discharge Improved motor exam Serum: elevated salivary protein 1 IgM, elevated carbonic anhydrase VI IgG and IgM antibodies, elevated parotid specific protein IgA antibody MRI brain: persistent enhancement of cranial nerves 3-day course of high-dose oral prednisone
Residual numbness Ofatumumab 20 mg monthly

CSF: cerebrospinal fluid; MRI: magnetic resonance imaging; FLAIR: fluid-attenuated inversion recovery; IV: intravenous; SSB: Sjogren’s syndrome B.