Orthostatic intolerance is occasionally reported by patients with syringomy
elia and is usually attributed to vestibular symptoms or neurogenic orthost
atic hypotension. Postural tachycardia syndrome has not been previously des
cribed in syringomyelia. A patient with long-standing syringomyelia and a C
hiari type I anomaly developed disabling "panic-like" attacks associated to
orthostatic intolerance five years after posterior fossa decompression and
shunting of the syrinx. A head-up tilt test showed an early phase of postu
ral orthostatic tachycardia followed by progressive arterial hypotension an
d bradycardia as seen in neurally mediated syncope. A magnetic resonance im
aging scan showed a collapsed syrinx from the 3rd cervical to the 12th thor
acic vertebra without syringobulbia. Fludrocortisone and beta -blockers led
to resolution of symptoms. Partial sympathetic denervation of the legs in
syringomyelia might explain the occasional occurrence of postural tachycard
ia syndrome. Postural tachycardia syndrome may be included as a possible ca
use of orthostatic symptoms in syringomyelia patients.