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. 2021 Feb 25;40:102000. doi: 10.1016/j.tmaid.2021.102000

Table 1.

Clinical, laboratory and neuroimaging features in COVID-19 patients with acute myelopathies.

Case 1 Case 2 Case 3
Subject demographics Female, 25 y-o Female, 50 y-o Male, 69 y-o
Medical history Essential tremor Hypertension, dyslipidemia
COVID-19 symptoms Mild (fever, anosmia, dysgeusia) Mild (fever) Moderate (fever, asthenia, interstitial pneumonia)
Exposure to proven COVID-19 cases Untraceable Workmates Wife
COVID-19 treatment Acetaminophen HCQ 200 mg bid for 7 days, azithromycin 500 mg for 5 days, amoxicillin/clavulanate 875/125 mg bid for 7 days and celecoxib Amoxicillin/clavulanate 875/125 mg bid for 2 days
CNS Neurological features Sub-acute paraplegia, sensory impairment with upper thoracic level, bladder dysfunction Sub-acute sensorimotor impairment to the lower limbs with gait ataxia Acute flaccid paraplegia, sensory impairment with mid thoracic level, bladder and bowel dysfunction
Latency/Overlap between infectious and neurological onset 15 days/No 15 days/No 3 days/Yes
Lab tests (at admission) Normal Normal WBC 6,6/mmc
Ly 1,2/mmc
CRP 151 mg/l
Ferritin 1422 ng/ml
LDH 592 U/L
Chest imaging during hospitalization Negative Negative Interstitial pneumonia
SARS-CoV-2 RT-PCR (swab) – performed after symptom onset: Positive Negative (not performed during the infectious course) Positive
  • -

    Infectious

20 days 30 days 3 days
  • -

    Neurological

5 days 15 days <1 day
Brain neuroimaging MRI: Normal findings MRI: Single periventricular lesion (Fig. 1, II) MRI: Single lesion in the left superior cerebellar peduncle (Fig. 1, III)
Spine neuroimaging MRI: Multiple lesions (cervical and thoracic spinal cord) (Fig. 1, I) MRI: Two lesions (one extending from the bulbo-medullary junction down to C6, one located at the conus) (Fig. 1, II) MRI: Multiple lesions (cervical and upper thoracic spinal cord, LETM extending from mid-thoracic down to the epiconus)
(Fig. 1, III)
CSF findings Slight lymphomonocytic pleocytosis (8 cells/mmc), no OCBs Moderate lymphomonocytic pleocytosis (65 cells/mmc), hyperproteinorrachia (161.2 mg/dl), slight hypoglycorrachia (41 mg/dl), no OCBs Marked neutrophilic pleocytosis (672 cells/mmc), hyperproteinorrachia (90 mg/dl), normal glucose, “mirror pattern” OCBs.
Control CSF (after 5 days): reduced pleocytosis (26 cells/mmc) and hyperproteinorrachia (58 mg/dl), normal glucose, no OCBs
Neurophysiology Motor evoked potentials: temporal dispersion, normal central conduction times.
EMG/ENG: normal.
Somatosensory evoked potentials: delayed latency for cortical response with lower limbs stimulation.
EMG/ENG: normal.
Motor evoked potentials: no response for lower limbs.
EMG/ENG: “polio-like syndrome” in lower limbs (reduced amplitude of compound motor action potentials, reduced recruitment pattern, presence of denervation potentials on needle EMG, absent F wave responses)
SARS-CoV-2 RT-PCR on CSF Negative N.P. Negative
Diagnosis Post-infectious demyelinating myelitis Post-infectious encephalomyelitis Para-infectious demyelinating and polio-like encephalomyelitis
Treatment M-P 1 g OD for 7 days Ceftriaxone 2 g x 2 for 5 days,
Ampicillin 2 g x 6 for 5 days,
Acyclovir 750 mg x 3 for 3 days
M-P 1 g OD for 5 days, 500 mg OD for 3 days, 250 mg OD for 3 days
Ceftriaxone 2 g x 2 for 10 days, acyclovir 750 mg x 3 for 5 days, lopinavir/ritonavir 400/100 mg and HCQ 200 mg x 2 for 14 days
M-P 1 g OD for 7 days; IVIg 0.4 g/kg OD for 5 days
Clinical follow up After 2 weeks; discharged to rehab with paraplegia and sensory gait ataxia, able to walk with a walker
After 3 months:
Discharged home, able to walk with a walker, mild sensory gait ataxia
After 2 weeks: discharged to rehab with moderate gait ataxia
After 3 month:
Slight gait ataxia, able to walk without devices
After 3 weeks: discharged to rehab with severe paraplegia, unable to stand
After 3 months:
Still in rehab, moderate improvement of strength, able to walk with a walker and assistanc

Abbreviations: y-o, year-old; F, female; M, male; CNS, central nervous system; Ly, lymphocytes; CSF, cerebrospinal fluid; OCBs, oligoclonal bands; LETM, longitudinal elongated transverse myelitis; N.P., not performed; OD, omne in die; bid, bis in die; M-P, methylprednisolone; HCQ, hydroxychloroquine; IVIg, intravenous immunoglobulins.