key: cord-0914152-9dldbs6o
authors: El-Zein, Rayan S; Cardinali, Serge; Murphy, Christie; Keeling, Thomas
title: COVID-19-associated meningoencephalitis treated with intravenous immunoglobulin
date: 2020-09-06
journal: BMJ Case Rep
DOI: 10.1136/bcr-2020-237364
sha: d5b0df08e64e65a59e140afbe67f65701b96e728
doc_id: 914152
cord_uid: 9dldbs6o

A 40-year-old man presented with altered mental status after a recenthospitalisation for COVID-19 pneumonia. Cerebrospinal fluid (CSF) analysis showed lymphocytosis concerning for viral infection. The CSF PCR for SARS-CoV-2 was negative, yet this could not exclude COVID-19 meningoencephalitis. During hospitalisation, the patient’s mentation deteriorated further requiring admission to the intensive care unit (ICU). Brain imaging and electroencephalogram (EEG) were unremarkable. He was, thus, treated with intravenous immunoglobulin (IVIg) for 5 days with clinical improvement back to baseline. This case illustrates the importance of considering COVID-19’s impact on the central nervous system (CNS). Haematogenous, retrograde axonal transport, and the effects of cytokine storm are the main implicated mechanisms of CNS entry of SARS-CoV-2. While guidelines remain unclear, IVIg may be of potential benefit in the treatment of COVID-19-associated meningoencephalitis.

A growing body of evidence is surfacing in regard to the neuroinvasiveness of COVID-19. Neurologic manifestations in patients infected with SARS-CoV-2 have been reported such as anosmia, ageusia, ataxia, seizures, haemorrhagic necrotising encephalopathy, and Guillain-Barré syndrome. [1] [2] [3] The neurotropism of COVID-19 remains undefined, although, previous coronaviruses have been implicated to involve the central nervous system (CNS). 4 Herein, we present a case of a patient with altered sensorium diagnosed with COVID-19associated meningoencephalitis.

A 40-year-old Hispanic man with no known medical history reported fevers, cough, and generalised fatigue in early April 2020 (day 1). On day 3, he presented to the emergency department and was confirmed to have COVID-19 via detection of SARS-CoV-2 viral nucleic acid in a nasopharyngeal swab specimen using the Simplexa SARS-CoV-2 assay (Diasorin Molecular LLC, Cypress, California, USA). He was subsequently hospitalised for 7 days for COVID-19-associated pneumonia. He completed a regimen of hydroxychloroquine (200 mg every 12 hours for 5 days). One day after discharge (day 7), he returns to the hospital with altered mental status. The patient's son reported that he was responding to questions inappropriately, having visual hallucinations, and was forgetful. Neurological examination revealed confusion with orientation only to self, inability to follow commands,and no apparent focal neurological deficits. Otherwise, general examination was unremarkable and vital signs were within normal ranges (blood pressure 129/84 mm Hg, heart rate 104 bpm, SpO 2 98% on room air and 98.5°F oral temperature).

After an unrevealing CT of the head, a lumbar puncture was performed. His cerebrospinal fluid (CSF) was clear and colourless with an elevated CSF cell count and lymphocytic predominance suspicious for viral encephalitis (table 1). The CSF glucose (70 mg/ dL) was increased and CSF protein levels (19 mg/ dL) were decreased. A CSF PCR panel including Cryptococcus neoformans/gattii, herpes simplex virus, varicella zoster virus, Streptococcus pneumoniae, Neisseria meningitidis and enterovirus was negative. The SARS-CoV-2 CSF PCR was negative; however, a high index of suspicion remained due to the temporal relationship of his current symptoms and the recent COVID-19 pneumonia. Due to the patient's lack of risk factors, testing for tuberculous was not pursued, especially with the absence of an elevated CSF protein and decreased CSF glucose concentration. Also, mycoplasma studies were not performed. An empiric meningitis regimen (ceftriaxone, vancomycin, acyclovir and steroids) was initiated and he was admitted to the medical ward with the clinical diagnosis of encephalitis.

Blood analysis revealed an elevated ferritin (1127 ng/mL), lactate dehydrogenase (LDH) (295 U/L), and C reactive protein (10.6 mg/L). These are decreased in comparison with 2 days prior during his recent hospitalisation (ferritin 1225 ng/mL, LDH 355 U/L and CRP 58.2 mg/L). D-dimer was elevated at 1.42 µg/mL, which increased from 1.06 µg/mL. One day after admission (day 8), he was transferred to the intensive care unit (ICU) for progressively worsening mental status with increased agitation; a dexmedetomidine infusion was initiated. MRI of the brain did not reveal any significant alterations or contrastenhanced areas within the brain and/or meninges (figure 1). A routine electroencephalogram (EEG) showed diffuse slowing in the theta range indicative of encephalopathy and lacked any epileptogenic activity. To this end, autoimmune encephalitis was less likely due to the absence of bilateral brain MRI New disease findings in addition to lack of epileptogenic or focal slowing observed on EEG. The antimicrobial regimen was deescalated; the CSF Gram stain and culture were negative.

Two days after admission (day 9), he was started on intravenous immunoglobulin (IVIg) (0.4 g/kg) for 5 days. For concern of delay in viral clearance, glucocorticoids were avoided. Within the next 2 days, his altered mentation progressively improved; he was oriented to time and place, able to communicate, and was following commands. He could not recall recent events of the hospital admission. On the third day of treatment, the patient was back at his baseline. After completion of IVIg, at discharge, 7 days after admission (day 14), neurological examination was unremarkable.

Two months after discharge, via a telephone follow-up encounter, the patient denied any symptoms. His son denied any further mental status changes.

Our report describes a case of encephalitis associated with SARS-CoV-2 which showed clinical improvement with IVIg therapy. There are only a few cases previously reported on the neurologic involvement of COVID-19 with variable presentations, diagnostics and treatments. Moriguchi et al 5 described what appears to be the first case of COVID-19-associated meningoencephalitis presenting with convulsions and confirmed with a positive SARS-CoV-2 CSF PCR; their patient had abnormal MRI findings of the medial temporal lobe and was treated with favipiravir. The patient remained in ICU at day 15 after onset of symptoms. Another report described a case of COVID-19associated necrotising encephalopathy with multiple haemorrhagic rim enhancing lesions on MRI. 2 They used IVIg as the mainstay therapy but the outcome remained undefined. Paniz-Mondolfi et al 6 reported a case of COVID-19-associated pneumonia in a 74 years old with Parkinson's who succumbed to his illness on day 11; however, SARS-CoV-2 was found in the brain capillary endothelium and neuronal cell bodies on postmortem examination.

Large studies pertaining to the incidence, diagnostics, and therapeutics of COVID-19 neurologic manifestations remain lacking. A recent retrospective study showed that approximately 55 (25%) of 214 patients with COVID-19 had manifestations of CNS involvement with dizziness and headache being the most common. 1 CSF analysis was not performed in this cohort. In another retrospective study by Li et al, the incidence of cerebrovascular events in patients with COVID-19 was about 5% with a median time of stroke after COVID-19 diagnosis of 12 days. 1 As previously reported, 7 a subset of patients with COVID-19 could have neurologic signs and symptoms without the typical respiratory symptoms. As more reports emerge, there is a newfound interest in elucidating the mechanisms of SARS-CoV-2 neurotropism.

Lessons from the taxonomically related SARS-CoV 8 in the past have supported haematogenous spread and retrograde neuronal transport as the proposed routes of SARS-CoV-2 neuroinvasion. SARS-CoV-2, through its interaction with ACE2, could enter the CNS given that ACE2 is expressed in the vascular endothelium, neurons, and glial cells of the brain. 9 Under electron microscopy, SARS-CoV-2 viral particles have been shown to be actively budding across endothelial cells of frontal lobe brain sections. 6 The cytokine storm associated with COVID-19 may alter the permeability of the blood-brain barrier, thus further allowing entry. Retrograde propagation along the olfactory tract has been shown to occur by SARS-CoV, and thus may explain the anosmia associated with SARS-CoV-2. 10 Once within the CNS, viral-induced cytokine storm and glial cell activation may result in immunologic response and inflammatory injury leading to encephalitis in our patient. Although the CSF PCR was negative, this could not definitely exclude the diagnosis because SARS-CoV-2 dissemination is transient and its CSF titre may be extremely low, as shown in cases of West Nile and enterovirus infections. 11 12 Our successful use of IVIg corroborates reporting of its possible benefit in COVID-19 13 14 ; no specific guidelines regarding its use are released as of yet. Considering the aforementioned inflammatory state undermining COVID-19, IVIg's proposed mechanism consists of the inhibition of innate immune cells, neutralization of activated complement, modulation of B cells and regulatory T cells, and the inhibition of cytokines. 15 Figure 1 Brain MRI demonstrating normal MRI findings on T2.

► COVID-19 may involve the central nervous system irrespective of pulmonary involvement. ► The cerebrospinal fluid PCR for SARS-CoV-2 cannot be used definitively to exclude COVID-19-associated meningoencephalitis. ► Intravenous immunoglobulin may be of potential benefit in COVID-19-associated meningoencephalitis.

Caution must be taken with its increased risk of thromboembolism especially given the reports of COVID-19 hypercoagulability. Currently, several randomised controlled trials evaluating the efficacy of high-dose IVIg therapy in severe COVID-19 have been initiated (NCT04350580, NCT04381858 and NCT04261426).

Twitter Rayan S El-Zein @Rayan_ElZein

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Acknowledgements The authors would like to acknowledge members of the team who cared for the patient including neurologist, Dr Shnehal Patel; intensivists, Dr Lucia Chowdhury and Dr Harvinder Gill and hospitalist, Dr Sudhir Duvuru.

Contributors RSE, SC and TK participated in the care of the patient. Report was written by RSE, SC and CM.

The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.Competing interests None declared.

Provenance and peer review Not commissioned; externally peer reviewed.This article is made freely available for use in accordance with BMJ's website terms and conditions for the duration of the covid-19 pandemic or until otherwise determined by BMJ. You may use, download and print the article for any lawful, non-commercial purpose (including text and data mining) provided that all copyright notices and trade marks are retained.

Rayan S El-Zein http:// orcid. org/ 0000-0002-1437-7082