Human parechovirus type 6 and Guillain-Barré syndrome: a case report.
Laura PellegrinelliS GambaraR MicheliS BindaE FazziE ParianiPublished in: Journal of neurovirology (2018)
A previously healthy 6-year-old boy was admitted to hospital with hypotonia and hyposthenia of lower limbs. Electromyography and slow motor nerve conduction velocity test identified a lower limb acute motor axonal neuropathy. Brain and spinal cord magnetic resonance imaging demonstrated multifocal cortical gray matter lesions in both cerebral hemispheres consistent with gray matter acute disseminated encephalitis otherwise with viral/Mycoplasma pneumoniae encephalitis, and signs of involvement of anterior nerve roots of the cauda equina consistent with Guillain-Barré syndrome. The patient resulted negative to routinely bacterial and viral investigations but positive to human parechovirus that sequence analyses confirmed as type 6. Intravenous immunoglobulins and methylprednisolone treatment were administered but did not relieve the symptoms of Guillain-Barré syndrome. The disease improved gradually over the next 3-month follow-up with a complete remission of both central and peripheral nervous system symptoms.
Keyphrases
- lower limb
- case report
- endothelial cells
- magnetic resonance imaging
- spinal cord
- liver failure
- spinal cord injury
- respiratory failure
- high dose
- induced pluripotent stem cells
- drug induced
- healthcare
- aortic dissection
- subarachnoid hemorrhage
- emergency department
- rheumatoid arthritis
- multiple sclerosis
- hepatitis b virus
- peripheral nerve
- disease activity
- brain injury
- ulcerative colitis
- mechanical ventilation
- combination therapy