Conus Medullaris-Cauda Arteriovenous Malformation and Klippel-Trenaunay Syndrome: What is the Treatment Goal?
Author:
Affiliation:
1. Neurosurgery Unit, Treviso Hospital, University of Padova
2. Department of Neurosurgery, Eiju General Hospital
3. Neuroradiology Unit, Treviso Hospital
4. Department of Neurosurgery, Fondazione IRCCS Istituto Neurologico “C. Besta”
Publisher
Japan Neurosurgical Society
Subject
Neurology (clinical),Surgery
Link
https://www.jstage.jst.go.jp/article/nmc/53/2/53_2012-0111/_pdf
Reference31 articles.
1. 1) Aelvoet GE, Jorens PG, Roelen LM: Genetic aspects of the Klippel-Trenaunay syndrome. Br J Dermatol 126: 603-607, 1992
2. 2) Alexander MJ, Grossi PM, Spetzler RF, McDougall CG: Extradural thoracic arteriovenous malformation in a patient with Klippel-Trenaunay-Weber syndrome: case report. Neurosurgery 51: 1275-1279, 2002
3. 3) Alomari AI, Orbach DB, Mulliken JB, Bisdorff A, Fishman SJ, Norbash A, Alokaili R, Lord DJ, Burrows PE: Klippel-Trenaunay syndrome and spinal arteriovenous malformations: an erroneous association. AJNR Am J Neuroradiol 31: 1608-1612, 2010
4. 4) Benhaiem-Sigaux N, Zerah M, Gherardi R, Bellot J, Hurth M, Poirier J: A retromedullary arteriovenous fistula associated with the Klippel-Trenaunay-Weber syndrome. A clinicopathologic study. Acta Neuropathol 66: 318-324, 1985
5. 5) Ceballos-Quintal JM, Pinto-Escalante D, Castillo-Zapata I: A new case of Klippel-Trenaunay-Weber (KTW) syndrome: evidence of autosomal dominant inheritance. Am J Med Genet 63: 426-627, 1996
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