Three months after the first symptoms his family physician prescribed magnetic resonance imaging (MRI) of the right shoulder, which was normal.
Three months later, electroneuromyography (ENMG) performed by the neurologist was highly suggestive of an isolated long thoracic axonal neuropathy. Bilateral ulnar and median nerve sensory conduction, motor conduction velocities, latencies, and F-wave incidence and latencies, were normal. Velocities were measured up to the level of the axilla. Stimulation of the right long thoracic nerve yielded a markedly reduced amplitude (1.0 mV) and slightly prolonged latency (4.1 m/s) compared to the left (5.7 mV and 3.9 m/s). Electromyographic needle examination of the right serratus anterior [5] showed decreased recruitment of compound motor unit action potential and maximum volitional activity; it was normal on the left.
Full blood count, iron studies, and vitamin B12 were normal. Serology was negative for cytomegalovirus IgM, HIV Ag p24, hepatitis B Ag HBs, hepatitis E virus IgM and IgG; it was positive for varicella zoster virus IgG, and borrelia IgM but not IgG. Western Blot confirmation of IgM was negative for proteins p17, p19, p21, p30, p31, p39, p83 and VLsE, but positive for p25 (= OspC), which is compatible for early infection or cross-reactions with herpes viruses. Given that symptoms were present for more than six months, borrelia is highly unlikely. Antibodies against SARS-CoV-2 were positive.
One week later an MRI of the cervical plexus did show integrity of the brachial plexus without hypersignal, contrast enhancement or compression, symmetrical muscles of the shoulder and scapula, without amyotrophy or oedema, normal and symmetrical serratus anterior, and moderate uncus and disk arthritis from C5 to C7 without spinal or foraminal narrowing or myelopathy. MRI of the brachial plexus is rarely abnormal in brachial plexus neuropathy or isolated long thoracic nerve palsy [6] although more recent analyses suggest that positive EMG findings can often be confirmed by MRI [7].
The clinical history, physical examination and neurophysiological findings strongly suggest an isolated neuropathy of the long thoracic nerve following vaccination against COVID-19. It could be a post-vaccine neuritis or a plexitis. Although the clinical history evokes a Parsonage-Turner syndrome or idiopathic brachial plexus neuropathy, typical signs of plexitis were absent and physical and electrophysiological abnormal findings were confined to the long thoracic nerve and the serratus anterior muscle. The patient didn’t present any signs or symptoms suggestive of a viral or bacterial infection known to be associated with post-infectious auto-immune neuritis (borrelia burgdorferi, cytomegalovirus, mycoplasma pneumoniae etc.). A discal prolapse or spondylolysis at the level of C5-C6 with compression of the anterior spinal cord or another cause of compression was excluded by MRI. The temporal sequence was highly suggestive of an adverse event following immunization (AEFI).
The prognosis of long thoracic nerve palsy is relatively good, with a third of patients recovering partially after one year and more than 50% after two years [8].
This patient was treated with physiotherapy and will be followed up every three months by the treating neurologist.