2019-20 coronavirus outbreak

Weakness

Surgery

Facial weakness

Virology

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)

Anesthesia

Outbreak

myalgia

Coronavirus disease 2019 (COVID-19)

Pediatrics

Electrophysiology

Muscle weakness

Infectious disease (medical specialty)

Internal medicine

Myositis

Bulbar palsy

Medicine

Physical medicine and rehabilitation

Guillain-Barre syndrome

Dysphagia

Compound muscle action potential

Disease

Electromyography

Repetitive nerve stimulation

Muscle & Nerve

Coronavirus disease-2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), is known for being a life-threatening respiratory illnesses, but there is increasing evidence of neurological manifestations.1 Herein we report a patient with COVID-19–associated inflammatory myopathy who presented with facial, bulbar, and proximal limb weakness. A 58-year-old woman presented with cough, dyspnea, and myalgia. Vital signs were stable and her physical examination was unremarkable. Initial polymerase chain reaction (PCR) testing for SARS-CoV-2 was negative and the patient was discharged home. She returned 3 weeks later with more severe dyspnea, cough, dysarthria, dysphagia, odynophagia, and severe generalized weakness with inability to ambulate. She had no sensory symptoms or bowel or bladder dysfunction. Physical examination was significant for tachycardia at 110 beats/min and oxygen saturation of 88% on room air. She had bilateral ptosis, facial weakness, hypernasal dysarthria, and profound symmetric proximal limb weakness. Reflexes were symmetrically diminished. Repeat SARS-CoV-2 PCR test was positive. MRI of the entire neuroaxis showed no central or peripheral nervous system involvement, but it did demonstrate diffuse muscle edema and enhancement, with a region of myonecrosis (Figure 1A,B). Motor nerve conduction studies of the peroneal, tibial, ulnar, and median nerves were unremarkable, as were sensory studies of the ulnar and median nerves; no responses were elicited from the superficial peroneal and sural nerves. Three-hertz repetitive stimulation of the ulnar nerve before and after 1-minute exercise showed no change in compound muscle action potential amplitude recorded from the abductor digiti minimi muscle during a series of 10 stimuli. Needle electromyography of the right vastus lateralis, iliopsoas, and deltoid muscles revealed sparse fibrillation potentials; no motor units could be activated. On admission, creatine kinase (CK) was elevated to 700 U/L. Anti–Sjögren-syndrome–related antigen (anti-SSA) and anti–small ubiquitinlike modifier-1–activating enzyme (anti–SAE 1) antibodies were both strongly positive and Ku antibody was weakly positive. Acetylcholine receptor (AChR) binding, modulating, and muscle-specific kinase (MuSK) antibodies were all negative (Table 1). Muscle biopsy showed perivascular inflammatory infiltration with endomysial extension, regenerating fibers, and upregulation of human leukocyte antigen class ABC expression on non-necrotic fibers. Cytochrome oxidase/succinic dehydrogenase enzyme histochemistry was unremarkable. Vacuolar change and curvilinear bodies (on electron microscopy) suggestive of hydroxychloroquine myopathy were absent (Figure 1C-F). Our presumptive diagnosis was COVID-19–associated myositis and a 5-day course of 1000 mg intravenous methylprednisolone was administered. Elevated interleukin-6 was found and tocilizumab was given. Anticoagulation was given for left brachial vein thrombosis and a 5-day course of hydroxychloroquine and azithromycin was also administered. Over 2 weeks, her CK levels normalized and she recovered the ability to raise her arms and legs from the bed. She showed slow improvement in bulbar function and her speech became more intelligible. She did not require mechanical ventilation; however, a percutaneous endoscopic gastrostomy (PEG) tube was inserted to allow for sufficient nutrition. Viral infection is a well-known cause of myositis in which influenza A and B are the most common causes in the United States.2 Myopathy with elevated CK levels has been reported in patients with severe acute respiratory syndrome (SARS).3 Limited pathological studies suggested vasculitis or immune-mediated mechanism as the potential cause for myopathy, without evidence of direct viral invasion.4, 5 Myalgias have been reported in up to a half of the patients with SARS-CoV-2 infection. Serum CK levels elevations depend on the severity of disease, ranging from mild to frank rhabdomyolysis.1, 6-8 A recent report described a COVID-19 patient with myalgia, proximal weakness, elevated CK level, and muscle edema on MRI.9 Herein we have reported a COVID-19 patient with associated myositis involving the proximal limb, bulbar, and facial muscles. The severe immune activation known to occur in COVID-19 patients likely plays a major pathophysiological role. Myositis and myasthenia gravis (MG) may coexist and, although specific antibodies were negative and ulnar repetitive nerve stimulation was normal, the severe bulbar involvement raises the possibility of superimposed MG. This is especially of interest in light of a recent report of patients with MG and COVID-19, one of whom was successfully extubated after treatment with tocilizumab.10 Direct viral invasion was not detected by electron microscopy. The finding of multiple serologic autoimmune antibodies is intriguing, suggesting an epiphenomenon rather than activation or unmasking of a specific immune response directed to the muscles. Further studies are needed to elucidate the mechanisms, appropriate treatment, and long-term clinical outcomes of muscular manifestations associated with COVID-19. The authors declare no potential conflicts of interest. We confirm that we have read the Journal's position on issues involved in ethical publication and affirm that this report is consistent with those guidelines.

<scp>COVID</scp>‐19–associated myositis with severe proximal and bulbar weakness

COVID‐19–associated myositis with severe proximal and bulbar weakness