Abstract
BackgroundLewis-Sumner Syndrome (LSS) is considered an asymmetric sensory-motor variant of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP), mostly affecting the limbs distally, with electrophysiological evidence of multifocal motor conduction blocks. Cranial nerve involvement is present in a minority. Various well-known infectious agents, directly or via the host’s immune responses, may trigger or exacerbate acute and chronic peripheral neuropathies, which may manifest clinically through a multitude of signs and symptoms.Case presentationWe present the case of a 57-year-old male with Lewis-Sumner Syndrome, whose clinical course was quite stable over many years. He developed severe hyperacute relapse of his neuropathic disease in the context of active pneumonia due to influenza A (H1N1) virus infection. During this exacerbation, besides the obvious worsening of the previous asymmetric limb involvement, the patient also manifested left peripheral facial palsy and dysphagia that rapidly evolved over minutes, mimicking a stroke. The patient also showed rapid recovery, with marked improvement of the acute neuropathic dysfunction, immediately after initiation of treatment with oseltamivir. Our hypothesis is that the direct modulation of Na + ion channel activity in the host’s peripheral nerve cell by H1N1 viral proteins could cause acute and potentially reversible dysfunction in the conduction of nerve action potentials. Direct viral neuritis could also have been the cause. Immunomodulatory agents, namely IVIg, were not administered due to the swift clinical improvement noticed in the following days.ConclusionsWe aim to raise awareness of the possibility of atypical neurological presentations of viral infections, especially relevant in the context of the pandemic the world is now facing.
Highlights
Lewis-Sumner Syndrome (LSS) is considered an asymmetric sensory-motor variant of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP), mostly affecting the limbs distally, with electrophysiological evidence of multifocal motor conduction blocks
* Correspondence: luismiggr@gmail.com 1Department of Neurology, Unidade Local de Saúde de Matosinhos, Hospital Pedro Hispano, Sra. da Hora, Portugal Full list of author information is available at the end of the article half the patients and cranial nerve involvement is present in a minority
Various well-known infectious agents, directly or via the host’s immune responses, may be the trigger of acute and chronic peripheral neuropathies, or of their clinical exacerbation, which may manifest through a multitude of signs and symptoms [2,3,4,5]
Summary
Lewis-Sumner Syndrome (LSS) is considered an asymmetric sensory-motor variant of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP), mostly affecting the limbs distally, with electrophysiological evidence of multifocal motor conduction blocks. Background Lewis-Sumner Syndrome (LSS) is considered an asymmetric sensory-motor variant of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP), affecting the limbs mostly distally, with electrophysiological evidence of multifocal motor conduction blocks. * Correspondence: luismiggr@gmail.com 1Department of Neurology, Unidade Local de Saúde de Matosinhos, Hospital Pedro Hispano, Sra. da Hora, Portugal Full list of author information is available at the end of the article half the patients and cranial nerve involvement is present in a minority.
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