Abstract
Paroxysmal sympathetic hyperactivity (PSH) is not a well-recognized syndrome in pediatric
brain tumors, but has been described in adults with traumatic brain injury. We describe
the case of a child with medulloblastoma presenting with PSH. An index of suspicion
is important in early diagnosis of PSH and this ultimately has an impact on the long-term
outcome of patients with the syndrome.
Keywords
Dysautonomia - Medulloblastoma - paroxysmal sympathetic hyperactivity - Pediatric
brain tumors