Though detected with increasing frequency, intracranial carotid artery
dissection remains less common in infancy. We report on 3 otherwise h
ealthy children aged 8, 12 and 15 years who presented with focal heada
che and stroke secondary to intracranial carotid occlusive disease con
sistent with arterial dissection. In 2 cases this was precipitated by
strenuous physical exertion. The protean angiographic configuration in
cluded long tapered narrowing with focal stenosis, beaded narrowing wi
th Moya Moya vascular network and 'string sign'; occlusion of the ante
rior cerebral artery was always present. Control angiograms revealed c
omplete or partial recanalization in all cases suggesting self-healing
dissection. The clinical course was smooth in all patients, and at lo
ng-term follow-up (5, 3, and 2 years) they remain in good neurological
condition. Although intracranial carotid dissection has a poor reputa
tion, regression to normal and fair outcome may sometimes occur as in
the extracranial counterpart, suggesting the existence of benign forms
of the disease. Surgical procedures should be weighed against the spo
ntaneous resolution of the lesion.