Serial Imaging of Virus-Associated Necrotizing Disseminated Acute Leukoencephalopathy (VANDAL) in COVID-19
==========================================================================================================

* S. Agarwal
* J. Conway
* V. Nguyen
* S. Dogra
* P. Krieger
* D. Zagzag
* A. Lewis
* K. Melmed
* S. Galetta
* R. Jain

## Abstract

**BACKGROUND AND PURPOSE:** Various patterns of leukoencephalopathy have been described in coronavirus disease 2019 (COVID-19). In this article, we aimed to describe the clinical and imaging features of acute disseminated leukoencephalopathy in critically ill patients with COVID-19 and the imaging evolution during a short-term follow-up.

**MATERIALS AND METHODS:** We identified and reviewed the clinical data, laboratory results, imaging findings, and outcomes for 8 critically ill patients with COVID-19 with acute disseminated leukoencephalopathy.

**RESULTS:** All patients demonstrated multiple areas of white matter changes in both cerebral hemispheres; 87.5% (7/8) of patients had a posterior predilection. Four patients (50%) had short-term follow-up imaging within a median of 17 days after the first MR imaging; they developed brain atrophy, and their white matter lesions evolved into necrotizing cystic cavitations. All (8/8) patients had inflammatory cytokine release syndrome as demonstrated by elevated interleukin-6, D-dimer, lactate dehydrogenase, erythrocyte sedimentation rate, C-reactive protein, and ferritin levels. Most (7/8; 87.5%) patients were on prolonged ventilator support (median, 44.5 days; interquartile range, 20.5 days). These patients had poor functional outcomes (6/8 [75%] patients were discharged with mRS 5) and high mortality (2/8, 25%).

**CONCLUSIONS:** Critically ill patients with COVID-19 can develop acute disseminated leukoencephalopathy that evolves into cystic degeneration of white matter lesions with brain atrophy during a short period, which we dubbed virus-associated necrotizing disseminated acute leukoencephalopathy. This may be the result of COVID-19-related endothelial injury, cytokine storm, or thrombotic microangiopathy.

## ABBREVIATIONS:

ADEM
:   acute disseminated encephalomyelitis
ARDS
:   acute respiratory distress syndrome
CRP
:   C-reactive protein
COVID-19
:   coronavirus disease 2019
ESR
:   erythrocyte sedimentation rate
GCS
:   Glasgow Coma Scale
IL-6
:   interleukin-6
INR
:   international normalized ratio
IQR
:   interquartile range
LDH
:   lactate dehydrogenase
PRES
:   posterior reversible encephalopathy syndrome
SARS-CoV-2
:   Severe Acute Respiratory Syndrome coronavirus 2
VANDAL
:   Virus Associated Necrotizing Disseminated Acute Leukoencephalopathy
WM
:   white matter

Much of the focus regarding the global pandemic of coronavirus disease 2019 (COVID-19) has been on the cardiovascular, pulmonary, and hematologic complications. However, neurologic complications have become increasingly recognized sequelae, with associated high morbidity and mortality.1⇓⇓⇓-5 Although the current literature is limited regarding neuroimaging findings in patients with COVID-19,6⇓-8 there have been recent reports of critically ill patients with leukoencephalopathy with or without cerebral microhemorrhages.9⇓⇓⇓⇓-14 Different radiologic patterns of white matter (WM) injury have been described in critically ill patients with viral infections, including diffuse leukoencephalopathy with microhemorrhages, acute disseminated encephalomyelitis (ADEM), and posterior reversible encephalopathy syndrome (PRES).11,15⇓⇓⇓⇓-20 Due to a paucity of neuropathologic data, the pathophysiologic processes responsible for these imaging characteristics are not completely understood. A recent report on postmortem examination of 5 patients with COVID-19 did not reveal evidence of encephalitis or central nervous system vasculitis, but this series lacked neuroimaging.21 Another report suggested that the neuropathologic lesions in patients with COVID-19 had features resembling both vascular and demyelinating etiologies,22 but this report also lacked neuroimaging data to correlate with the neuropathologic findings.

In this article, we aimed to describe the clinical, laboratory, and functional outcomes of patients with COVID-19 with acute disseminated leukoencephalopathy on brain MR imaging, as well as the imaging evolution of these WM lesions. We examined possible underlying mechanisms for these findings.

## MATERIALS AND METHODS

We performed a retrospective chart review of 115 adult patients positive for COVID-19 who underwent brain MR imaging at 3 tertiary care hospital sites of a single academic medical center from March 1, 2020, to May 10, 2020, and found 8 patients with acute disseminated leukoencephalopathy, 4 (50%) of whom had >1 MR imaging, 3/4 (75%) who had 2, and 1/4 (25%) who had 3 MR imagings. MR images obtained on a 3T MR imaging scanner included susceptibility-weighted imaging, while those scanned on a 1.5T scanner had gradient-echo imaging. Of the 8 patients, 4 patients had imaging performed on both 1.5T and 3T MR imaging scanners. MRIs were evaluated independently by 2 fellowship-trained neuroradiologists (R.J. and V.N.). Imaging data on the pattern of distribution of the WM lesions and microhemorrhages were collected. Follow-up MR imaging studies were evaluated for progression or evolution of WM lesions and evidence of subjective brain atrophy, defined as an interval increase in the prominence of the ventricles and sulcal spaces due to brain volume loss compared with the baseline study.

S.A., S.D., and P.K. reviewed charts and collected the following data: comorbidities, presenting symptoms, time from symptom onset to presentation, vital signs, ventilator days before brain MR imaging, total ventilator days, the total length of hospitalization, treatment received for COVID-19, occurrence of in-house cardiac arrest, Glasgow Coma Scale (GCS) score at MR imaging and 2 weeks post-MR imaging, acute respiratory distress syndrome (ARDS) severity score (calculated as the lowest partial pressure of oxygen/fraction of inspired oxygen ratio while intubated).23 Functional outcomes included discharge mRS, discharge disposition, and death. Discharge mRS scores were calculated by trained physical therapists ≤5 days before discharge or determined by a neurology resident (S.A.) on the basis of the clinical notes when not otherwise documented. We collected laboratory variables including admission and nadir platelet count and fibrinogen levels and admission and peak D-dimer, lactate dehydrogenase (LDH), international normalized ratio (INR), erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), interleukin-6 (IL-6), and ferritin levels.

This study was approved by the New York University Grossman School of Medicine Institutional Review Board, which granted a waiver of informed consent (IRB No. i20-00567).

## RESULTS

All 8 patients with MR imaging findings of acute disseminated leukoencephalopathy were men, with a median age of 59.5 years (range, 38–69 years). Demographic and clinical features of individual patients are shown in the Online Supplemental Data. Although 2 patients had no known comorbidities, the remaining 6 had at least 3 comorbidities on admission. All patients presented with respiratory symptoms (fevers, chills, cough, and dyspnea) and had symptoms for a median of 7 days (range, 4–14 days) before presentation to the emergency department. All patients (100%) were treated with a combination of hydroxychloroquine and azithromycin, 62.5% (5/8) were also treated with tocilizumab, and 12.5% (1/8) were given lopinavir-ritonavir. Intubation was required for 87.5% of patients (7/8), and ventilator support was needed for a median of 44.5 days (range, 24–52 days). Of these 7 patients, 42.9% (3/7) had moderate and 42.9% (3/7) had severe ARDS. The peak systolic blood pressure before the first MR imaging ranged from 162 to 240 mm Hg. In-hospital cardiac arrest occurred in 37.5% (3/8) of patients, all of whom achieved a return of spontaneous circulation. Nearly all (87.5%; 7/8) patients developed acute kidney injury, and 62.5% (5/8) required continuous renal replacement therapy. At the time of the analysis of this study, 25% (2/8) of patients had died. There were no neuropathologic specimens available for analysis because postmortem examination was not performed.

These patients had cytokine storming as demonstrated by elevated median IL-6 (admission = 31 pg/mL [interquartile range (IQR) =15.5 pg/mL]; peak = 49 pg/mL [IQR = 73.5 pg/mL]; normal IL-6 levels = ≤5 pg/mL); D-dimer (admission = 2003 ng/mL [IQR = 2980 ng/mL]; peak = 8645 ng/mL [IQR = 4751.25 ng/mL); normal = D-dimer <230 ng/mL); LDH (admission = 492 U/L [IQR = 284 U/L]; peak = 970.5 U/L [IQR = 605.5 U/L]; normal LDH levels = 84–246 IU/L); ESR (admission = 83 mm/h [IQR = 60.5 mm/h]; peak = 117 mm/h [IQR = 27.75 mm/h]; normal ESR levels = 0–10 mm/h); CRP (admission = 113.5 mg/L [IQR = 106.43 mg/L]; peak = 336 mg/L [IQR 77.63 mg/L]; normal CFP levels = 0.0–3.0 mg/L); and ferritin (admission = 1070 ng/mL [IQR = 906.7 ng/mL]; peak = 4701.5 ng/mL [IQR = 11616.3 ng/mL]; normal ferritin levels = 8.0–388.0 ng/mL) (Online Supplemental Data).

Initial neuroimaging with brain MR imaging was performed at a median of 23.5 days (IQR = 5 days) since admission and, if intubated, 23 days (IQR = 6.5 days) after intubation. The indication for neuroimaging was persistent encephalopathy in nearly all (87.5%; 7/8) patients. Patients had a median GCS of 5 (IQR = 5.8) on the day of MR imaging, and there was no change in median GCS scores 2 weeks post-MR imaging. These patients had poor functional outcomes (75% of patients with discharge mRS of 5) and a high mortality rate (25%).

Neuroimaging showed multiple patchy areas of WM restricted diffusion/cytotoxic edema in both cerebral hemispheres, with a predilection for the posterior and subcortical regions in 87.5% (7/8) of patients. One of the 2 patients who received gadolinium demonstrated enhancement of the WM lesions suggesting BBB breakdown and evidence of central necrosis (Fig 1). Patchy lesions similar to WM lesions were also seen in the cerebellum (62.5%), brain stem (50%), and basal ganglia (25%) (Online Supplemental Data). Most (75%) patients also had microhemorrhages (Fig 1). Four patients underwent a follow-up MR imaging at a median of 35.5 days (IQR = 14.3 days) since admission and 17 days (IQR = 19.5 days) after the first MR imaging. Follow-up imaging in all 4 patients showed necrosis and development of small cystic cavitations in the WM lesions (which showed restricted diffusion/cytotoxic edema on the baseline study) and brain volume loss (Online Supplemental Data and Fig 2). Three patients also showed progression of WM lesions, which became more confluent (Fig 3). One patient who had 3 MR imaging studies showed sequential progression of the above WM findings on both follow-up studies.

![FIG 1.](http://www.ajnr.org/https://www.ajnr.org/content/ajnr/42/2/279/F1.medium.gif)

[FIG 1.](http://www.ajnr.org/content/42/2/279/F1)

FIG 1. 
Axial DWI (*A*) and T2-weighted imaging (*B*) showing disseminated leukoencephalopathy with associated microhemorrhages (*C*) seen on the susceptibility-weighted imaging. *D*, Postcontrast T1-weighted imaging shows patchy enhancement of most WM lesions, with the larger lesion in the left cerebral hemisphere also showing central nonenhancement, suggestive of breakdown of the BBB and WM necrosis.

![FIG 2.](http://www.ajnr.org/https://www.ajnr.org/content/ajnr/42/2/279/F2.medium.gif)

[FIG 2.](http://www.ajnr.org/content/42/2/279/F2)

FIG 2. 
*A* and *B*, Axial FLAIR and coronal T2-weighted images at baseline MR imaging (day 25) showing multiple confluent areas of leukoencephalopathy. *C* and *D*, These lesions progressed to show development of cystic cavitations in the WM (*arrows*) as well as interval prominence of the lateral and third ventricles, suggesting brain atrophy on follow-up MR imaging on day 75.

![FIG 3.](http://www.ajnr.org/https://www.ajnr.org/content/ajnr/42/2/279/F3.medium.gif)

[FIG 3.](http://www.ajnr.org/content/42/2/279/F3)

FIG 3. 
Axial DWI, T2-weighted, FLAIR *(A–C*), and coronal T2-weighted images (*D*) at baseline MR imaging (day 10) showing multiple patchy areas of restricted diffusion/cytotoxic edema in the WM. *E–H*, Axial corresponding follow-up MR imaging (day 75) demonstrates development of cystic cavitations in the previous patchy cytotoxic WM lesions (*arrows*) as well as interval prominence of the lateral and third ventricles, suggesting brain atrophy. Follow-up MR imaging also showed marked progression of more confluent WM lesions surrounding the patchy cystic lesions.

## DISCUSSION

We identified 8 critically ill patients with COVID-19 with acute disseminated leukoencephalopathy. This is the first study, to our knowledge, to show imaging evolution of acute disseminated leukoencephalopathy in patients with COVID-19. All patients who underwent follow-up imaging showed necrosis and cavitation of initial WM cytotoxic lesions as well as brain atrophy during their hospital stay within a fairly short follow-up period. Our findings suggest that this necrotizing leukoencephalopathy leads to rather rapid progression of extensive and permanent white matter damage and brain atrophy in these critically ill patients, which correlate very well with the poor functional outcomes shown in these patients.

Most (87.5%) of our patients had lesions that were predominantly posterior, similar to lesions seen in PRES. There have been reports of PRES in COVID-19,24,25 and while the MRI findings for our patients appear similar to those in PRES, they differ from those in PRES in that these WM changes are more patchy and deep, rather than confluent26 and progress rather than resolve on follow-up imaging.

Furthermore, while these lesions bear some similarity to other white matter lesions seen in patients with viral infections, such as acute necrotizing encephalitis27,28 or ADEM,29,30 they differ from these entities, as well. The WM lesions seen in patients in our study showed multiple diffuse confluent areas of T2/FLAIR hyperintensity, with diffusion restriction suggesting cytotoxic edema, which appears to be different from ADEM, in which these lesions are seen more often in subcortical regions with surrounding vasogenic edema. Thus, it appears that these lesions represent a previously undescribed finding, which we have dubbed virus-associated acute necrotizing disseminated leukoencephalopathy, or VANDAL, for short.

There have been serial brain MR imaging studies among critically ill patients without COVID-19 that have demonstrated global brain atrophy with preferential involvement of the superior frontal gyri, thalami, cerebellum, and hippocampal regions. The 4 patients in our study who had follow-up imaging showed brain atrophy. Although there have been no prior studies in patients with COVID-19 with serial imaging showing any evidence of brain atrophy, the findings seen in our patients could be due to either critical illness, hypoxic injury, or cytokine storming.31-33

Variable direct and indirect mechanisms of CNS injury due to COVID-19 could be responsible for these imaging findings.

### COVID-19–Related Endothelial Injury

Viral infections have been noted to cause endothelial damage leading to increased permeability of the BBB.15 Some pathologic studies in patients with COVID-19 have shown direct viral invasion of endothelial cells and diffuse endothelial inflammation,34 but more recent literature has suggested that these particles may have been misinterpreted as coronavirus and instead represent the rough endoplasmic reticulum.35 Severe Acute Respiratory Syndrome coronavirus 2 (SARS-CoV-2) binds directly to angiotensin-converting enzyme 2 receptors, which can cause weakening of the endothelial layer, leading to a breakdown of the BBB and subsequent dysfunction of autoregulation.36,37 Additionally, SARS-CoV-2 could lead to inflammation of the endothelial lining due to the recruitment of immune cells or hypoxic injury.38

PRES has been associated with endothelial dysfunction.39 In PRES, peak systolic blood pressure usually is between 170  and 190 mm Hg, but 10%–30% of patients have normal or only mildly elevated blood pressure.40,41 The peak systolic blood pressures in our patients ranged from 162 to 240 mm Hg. Thus, the imaging changes in our patients may be related to PRES, despite the absence of prolonged hypertension. While PRES usually resolves with time, 4 of our patients who had follow-up imaging were found to have progression of their WM lesions, suggesting that while this process may be related to PRES, it is different. Some of these deep, patchy WM lesions were present in the middle cerebral artery–posterior cerebral artery overlap area and could represent watershed ischemia due to hypoperfusion resulting from hypotension during cardiac arrest (experienced by 37.5% [3/8] of our patients) or hypotension secondary to sepsis. However, the posterior predominance of these lesions and the presence of lesions in the brain stem and cerebellum, areas not typically associated with watershed ischemia, make this mechanism of injury less likely.

### Cytokine Storm

Patients with COVID-19 who are critically ill have a massive inflammatory reaction believed to be due to accumulation of T-cells and macrophages, resulting in the release of a large number of cytokines into the bloodstream aiming to destroy the offending pathogen and resulting in numerous clinical manifestations known commonly as cytokine release syndrome.42,43 Classic laboratory findings of cytokine release include decreased T-cells and natural killer cells and, most important, an increase in IL-6, which leads to fever and multiorgan dysfunction. Higher levels of cytokines and interleukins have been postulated to be related to findings of disseminated leukoencephalopathy in patients with septic shock.44 These patients had laboratory evidence of cytokine storming, which could lead to BBB breakdown, promoting the development of acute disseminated leukoencephalopathy.

### Thrombotic Microangiopathy

Microhemorrhages in the subcortical WM and corpus callosum have been reported in high-altitude exposure and ARDS,45 and they are believed to be the result of disseminated intravascular coagulation. Microhemorrhages within afflicted posterior and subcortical WM may also be seen in PRES.26,46 In the population of critically ill patients with COVID-19, neuroimaging findings of diffuse leukoencephalopathy may be seen in conjunction with microhemorrhages, as is seen in some of our patients.7,10,11,47 The appearance of cotton wool spots and microhemorrhages on fundus examinations further suggests pathologic and ophthalmologic evidence of thrombotic microangiopathy in patients with COVID-19.48

Thus, endothelial dysfunction, cytokine storming, and thrombotic microangiopathy may contribute to the development of the acute disseminated leukoencephalopathy seen in patients with severe COVID-19 described herein. Of course, these factors could also lead to leukoencephalopathy with a variety of other imaging phenotypes. Acute disseminated necrotizing leukoencephalopathy appears to be a harbinger of poor outcome in patients with severe COVID-19, but it is unclear how patients with acute disseminated necrotizing leukoencephalopathy will compare with patients with other COVID-19-asscoiated WM changes during a long period.

Limitations of the current report include a small sample size, retrospective data collection, and a lack of histopathologic data. Nevertheless, there have been other neuropathologic studies published recently that support our findings and provide insight into the neurotropism of SARS-COV-249 and the potential parainfectious processes affecting the neural tissue in COVID-19.22 Further neuropathologic studies that include clinical and imaging data are needed to better understand these findings.

## CONCLUSIONS

Critically ill patients with COVID-19 may develop extensive and disseminated leukoencephalopathy, which evolves into cystic/cavitatory necrotizing lesions during a short time period with brain atrophy, correlating with the poor functional outcome in these patients. We believe that these lesions occur as a result of endothelial dysfunction, cytokine storming, and thrombotic microangiopathy. Because these findings appear to be inconsistent with any previously described neuropathology, we have dubbed this virus-associated necrotizing disseminated acute leukoencephalopathy (VANDAL). Histopathologic studies as well as long-term follow-up studies are needed to better understand this phenotype of leukoencephalopathy and determine if and how this is different from other WM changes in patients with COVID-19.

## Footnotes

*   Disclosures: Ariane Lewis—*UNRELATED*: *Expert Testimony*; *Other*: Deputy Editor for *Neurology* and *Seminars in Neurology*. Steven Galetta—*UNRELATED*: *Consultancy*: Genentech, Biogen. Rajan Jain—*UNRELATED*: *Consultancy*: Cancer Panels; *Royalties*: Thieme.

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*   Received August 11, 2020.
*   Accepted after revision September 16, 2020.


*   © 2021 by American Journal of Neuroradiology