Reflex sympathetic dystrophy syndrome is a troublesome, complex disord
er that presents with chronic, unexplained aching or burning pain, the
intensity of which is incommensurable with the original injury. Six d
iagnostic criteria have been described by Genant et al1: pain and tend
erness in the extremities; swelling of soft tissue; diminished motor f
unction; trophic skin changes; vasomotor instability; and patchy osteo
porosis. Currently, the most widely accepted etiology is an initial va
somotor reflex spasm occurring after an injury to the extremity, follo
wed by a loss of vascular tone, persistent vasodilation, and rapid bon
e resorption.2