Twenty-seven years follow-up of a patient with congenital

Eur. J. Med. Res. · Feb 2010

Case Reports

Twenty-seven years follow-up of a patient with congenital retinocephalofacial vascular malformation syndrome and additional congenital malformations (Bonnet-Dechaume-Blanc syndrome or Wyburn-Mason syndrome).

Follow-up of vascular changes in a patient with congenital retinocephalofacial vascular malformation syndrome. ⋯ Patients with retinal arteriovenous malformations should be early examined with neuroradiological methods.

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- Dieter Schmidt, H Agostini, and M Schumacher.
- University Freiburg, Augenklinik, Killianstr. 5, 79106 Freiburg, Germany. Dieter.Schmidt@uniklinik-freiburg.de
- Eur. J. Med. Res. 2010 Feb 26;15(2):89-91.
PurposeFollow-up of vascular changes in a patient with congenital retinocephalofacial vascular malformation syndrome.MethodsMRI and cerebral angiography.ResultsIn a 36-year-old man, magnetic resonance imaging of the skull and cerebral angiography revealed left intracranial arteriovenous malformations. Follow-up observation of 27 years revealed no essential change of retinal and cerebral arteriovenous malformations. Additional congenital deficits in this patient were described.ConclusionPatients with retinal arteriovenous malformations should be early examined with neuroradiological methods.

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Twenty-seven years follow-up of a patient with congenital retinocephalofacial vascular malformation syndrome and additional congenital malformations (Bonnet-Dechaume-Blanc syndrome or Wyburn-Mason syndrome).

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