| Literature DB >> 27015132 |
Arya N Bagherpour1, Gustavo J Rodriguez2, Chetan Moorthy3, Todd T Trier4, Alberto Maud2.
Abstract
Parkes Weber syndrome (PWS) is a congenital overgrowth disorder characterized by unilateral limb and axial hypertrophy, capillary malformations of the skin, and high-flow arteriovenous fistulas (AVFs). Spinal AVFs in the setting of PWS are challenging vascular lesions that often contain multiple arteriovenous (AV) shunts. The present case report highlights an adolescent girl with PWS who presented with a ruptured complex high-flow conus medullaris AVF. She was successfully treated with endovascular embolization and microsurgery. At the 2-year follow-up, the patient remained free of neurological symptoms and had no recurrence of the vascular malformation.Entities:
Keywords: AV = arteriovenous; AVF = AV fistula; AVM = AV malformation; DSA = digital subtraction angiography; KTS = Klippel-Trenaunay syndrome; NBCA = N-butyl cyanoacrylate; PWS = Parkes Weber syndrome; Parkes Weber Syndrome; SAH = subarachnoid hemorrhage; arteriovenous fistula; endovascular; spinal cord; treatment; vascular disorders; vascular malformation
Mesh:
Year: 2016 PMID: 27015132 DOI: 10.3171/2016.1.SPINE151156
Source DB: PubMed Journal: J Neurosurg Spine ISSN: 1547-5646