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Todd H. Alter, Thomas Helbig, Gino Chiappetta
  1. Department of Orthopaedic Surgery, Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey, United States.

Correspondence Address:
Todd H. Alter, Department of Orthopaedic Surgery, Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey, United States.

DOI:10.25259/SNI_192_2022

Copyright: © 2022 Surgical Neurology International This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

How to cite this article: Todd H. Alter, Thomas Helbig, Gino Chiappetta. Case report: Multiple sclerosis diagnosis after anterior lumbar interbody fusion and presumed COVID-19 infection. 31-Mar-2022;13:125

How to cite this URL: Todd H. Alter, Thomas Helbig, Gino Chiappetta. Case report: Multiple sclerosis diagnosis after anterior lumbar interbody fusion and presumed COVID-19 infection. 31-Mar-2022;13:125. Available from: https://surgicalneurologyint.com/?post_type=surgicalint_articles&p=11494

Date of Submission
21-Feb-2022

Date of Acceptance
17-Mar-2022

Date of Web Publication
31-Mar-2022

Abstract

Background: Multiple sclerosis (MS) is an autoimmune demyelinating disease of the central nervous system that may present with a wide variety of clinical presentations. However, there can be substantial overlap between symptoms from MS and those caused by lumbar spondylosis and/or postviral plexopathies.

Case Description: A 33-year-old female with a history of an L5-S1 anterior lumbar interbody fusion and exposure to the SARS-CoV-2 virus developed postoperative worsening of her symptoms interpreted as “radiculopathy.” Despite a subsequent L5-S1 fusion, she continued to neurologically deteriorate and was ultimately diagnosed with MS.

Conclusion: The initial symptoms/signs of MS may mimic lumbar radiculopathy and or postviral plexopathy (i.e., due to recent COVID-19). This report should serve as a warning to future spinal surgeons to better differentiate between radicular and other “complaints,” sufficient to avoid unnecessary repeated spinal surgery.

Keywords: Anterior lumbar interbody fusion, COVID-19, Lumbar, Multiple sclerosis, Myelopathy, Spine, Radiculopathy

INTRODUCTION

Because multiple sclerosis (MS) can produce a wide array of neurological symptoms, it can mimic a variety of other conditions. These include myelopathy attributed to vertebral disc herniation, spinal stenosis, or spondylosis, and more recently COVID-19-related viral plexopathy.[ 9 ] Further, there is increasing evidence that viral infections such as COVID-19 (i.e., with neuroinvasive potential leading to a pro-inflammatory state) can trigger MS exacerbations.[ 1 , 6 ] Here, we report a 33-year-old female who underwent lumbar surgery (anterior lumbar interbody fusion [ALIF]) and subsequently had COVID-19. Her postoperative symptoms/signs led to a revision of her lumbar spinal surgery, but were ultimately attributed to MS.

CASE

History

A 33-year-old female with a medical history of hypothyroidism, polycystic ovarian syndrome, pseudotumor cerebri, pacemaker placement for bradycardia, a gastric sleeve, and a C6-7 cervical disc replacement (1 year prior for myelopathy), presented with 2 years of low back pain/radiculopathy. On examination, she exhibited significant isolated weakness in her right lower extremity without sensory or reflex abnormalities [ Table 1 ]. Lumbar X-rays and an MRI showed moderate degenerative disc disease at the L5-S1 level, a 3 mm minimal degenerative retrolisthesis, and a right paracentral L5-S1 disc protrusion causing moderate lateral recess narrowing [ Figures 1 and 2 ]. She underwent an L5-S1 ALIF without complication [ Figure 3 ].


Table 1:

Summary of clinical data.

 

Figure 1:

(a) Anteroposterior radiographs of the lumbar spine. (b) Lateral radiographs of the lumbar spine.

 

Figure 2:

(a) Sagittal T2-weighted MRI image of the lumbar spine. (b) Axial T2-weighted MRI image of the lumbar spine.

 

Figure 3:

(a) Postoperative anteroposterior radiograph of the lumbar spine demonstrating anteriorly placed interbody cage at the L5-S1 level. (b) Postoperative lateral radiograph of the lumbar spine demonstrating anteriorly placed interbody cage at the L5-S1 level.

 

Postoperative course

One week postoperatively, she had fevers, but a postoperative CT of the abdomen and laboratory studies were normal. Shortly thereafter, her husband tested positive for COVID-19; she was not tested at that time. Two weeks postoperatively, she complained of new left leg paresthesias (i.e., note her prior deficits were right-sided) with weakness and diffusely decreased sensation to light touch. She was given a steroid taper and sent for a lumbar CT scan that “suggested” encroachment on the left L5-S1 neural foramen by the L5-S1 ALIF [ Figure 4 ]. Of interest, the MRI showed an intramedullary “lesion” at the L1-2 level in the area of the conus medullaris of unclear significance [ Figure 5 ].


Figure 4:

(a) Sagittal CT image demonstrating alignment of L5-S1 interbody cage. (b) Axial CT image demonstrating alignment of L5-S1 interbody cage.

 

Figure 5:

Sagittal T2-weighted MRI image of the lumbar spine.

 

Revision surgery followed by diagnosis of MS versus poly-sensory neuropathy

She then underwent a revision ALIF for cage repositioning. Postoperatively, her symptoms continued to worsen. MRIs of the cervical, thoracic spine, and brain were all normal along with multiple lab tests. She was sent home, but was now wheelchair bound. Repeat X-rays showed good location of the L5-S1 ALIF cage [ Figure 6 ]. A neurologist performed an EMG of the left lower extremity and determined that her deficit was likely consistent with transverse myelitis and/or a poly-sensory neuropathy (i.e., bilateral superficial peroneal and sural nerves).


Figure 6:

(a) Postoperative anteroposterior radiograph of the lumbar spine demonstrating anteriorly placed interbody cage at the L5-S1 level. (b) Postoperative lateral radiograph of the lumbar spine demonstrating anteriorly placed interbody cage at the L5-S1 level.

 

Delayed diagnosis of MS

Four months later, now with additional bilateral upper and lower extremity weakness/sensory loss, and worsening urinary urgency with incomplete bladder emptying, she underwent a complete spinal Myelo-CT; it was negative. However, the cerebrospinal fluid obtained from the lumbar puncture showed findings consistent with MS (i.e., primary progressive subtype). She then began MS modifying therapy.

DISCUSSION

Diagnosis of MS versus spinal pathology and risks of spine surgery precipitating demyelinating events

The diagnosis of MS can easily be missed when patients present with myelopathic symptoms misinterpreted as “radiculopathy” secondary to spinal pathology/spondylotic disease. In these cases, patients’ failures to improve with surgery were ultimately attributed to the underlying diagnosis of MS and may result in unintended exacerbation of MS (i.e., precipitate demyelinating events).[ 2 ] Further studies have shown that patients with known MS and significant spinal pathology may experience symptom improvement postoperatively, although the existing data are of low quality and conflicting [ Table 2 ].[ 8 ]


Table 2:

Summary of the literature reporting on surgical outcomes in patients with concomitant MS and spinal pathologies.

 

Increase in MS diagnoses related to COVID-19

Some have observed an increasing relationship between COVID-19 and the onset of MS (i.e., a spike in MS diagnoses).[ 4 , 5 , 7 ] Further, MS patients taking anti-CD20 disease modifying therapies may be the most at risk for developing COVID -19 infections (i.e., they generate a less robust immune response to the virus).[ 3 , 10 ] In this case, the patient’s lumbar surgeries and presumed infection with the SARS-CoV-2 virus may have directly triggered the onset/ flare of MS.

CONCLUSION

The diagnosis of MS can easily be missed when patients present with myelopathic symptoms misinterpreted as “radiculopathy” secondary to spinal pathology. Further, recent COVID-19 infections may pose triggers that potentiate the development of MS.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflict of interest.

References

1. Andersen O, Lygner PE, Bergström T, Andersson M, Vahlne A. Viral infections trigger multiple sclerosis relapses: A pros pective seroepidemiological study. J Neurol. 1993. 240: 417-22

2. D’hooghe MB, Nagels G, Bissay V, De Keyser J. Modifiable factors influencing relapses and disability in multiple sclerosis. Mult Scler. 2010. 16: 773-85

3. Möhn N, Konen FF, Pul R, Kleinschnitz C, Prüss H, Witte T. Experience in multiple sclerosis patients with COVID-19 and disease-modifying therapies: A review of 873 published cases. J Clin Med. 2020. 9: 4067

4. Moore L, Ghannam M, Manousakis G. A first presentation of multiple sclerosis with concurrent COVID-19 infection. eNeurologicalSci. 2021. 22: 100299

5. Palao M, Fernández-Díaz E, Gracia-Gil J, RomeroSánchez CM, Díaz-Maroto I, Segura T. Multiple sclerosis following SARS-CoV-2 infection. Mult Scler Relat Disord. 2020. 45: 102377

6. Sadeghmousavi S, Rezaei N. COVID-19 and multiple sclerosis: Predisposition and precautions in treatment. SN Compr Clin Med. 2020. 2: 1802-7

7. Satheesh NJ, Salloum-Asfar S, Abdulla SA. The potential role of COVID-19 in the pathogenesis of multiple sclerosis-a preliminary report. Viruses. 2021. 13: 2091

8. Yerneni K, Nichols N, Burke JF, Traynelis VC, Tan LA. Surgical management of patients with coexistent multiple sclerosis and cervical stenosis: A systematic review and meta-analysis. J Clin Neurosci. 2019. 65: 77-82

9. Young WF, Weaver M, Mishra B. Surgical outcome in patients with coexisting multiple sclerosis and spondylosis. Acta Neurol Scand. 1999. 100: 84-7

10. Zabalza A, Cárdenas-Robledo S, Tagliani P, Arrambide G, Otero-Romero S, Carbonell-Mirabent P. COVID-19 in multiple sclerosis patients: Susceptibility, severity risk factors and serological response. Eur J Neurol. 2021. 28: 3384-95

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