Acute, severe self-limiting dysautonomia and hypertensive encephalopathy

Pediatr Neurol. 2001 Oct;25(4):319-24. doi: 10.1016/s0887-8994(01)00316-2.

Abstract

We describe two unrelated children with almost identical clinical illnesses comprising of severe, burning dysesthesia, allodynia, hypertensive encephalopathy, and laboratory evidence of both sympathetic and parasympathetic autonomic disturbance after a nonspecific viral illness. No underlying etiology was identified. Both patients displayed complete resolution of their clinical and radiologic findings after a number of months, and there was no recurrence over a follow-up period of 17 months to 4 years. Treatment of the patients' dysesthesias proved difficult, requiring multiple analgesics and intensive physiotherapy. We speculate that their illnesses may represent a pure autonomic variant of Guillain-Barré syndrome.

Publication types

  • Case Reports

MeSH terms

  • Acute Disease
  • Adolescent
  • Autonomic Nervous System Diseases / complications*
  • Autonomic Nervous System Diseases / pathology
  • Brain / pathology*
  • Child
  • Diagnosis, Differential
  • Erythromelalgia / diagnosis
  • Female
  • Guillain-Barre Syndrome / diagnosis
  • Humans
  • Hypertensive Encephalopathy / complications
  • Hypertensive Encephalopathy / diagnosis*
  • Hypertensive Encephalopathy / pathology
  • Magnetic Resonance Imaging
  • Paresthesia / etiology
  • Seizures / etiology
  • Severity of Illness Index