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)

PURPOSE: Follow-up of vascular changes in a patient with congenital retinocephalofacial vascular malformation syndrome. METHODS: MRI and cerebral angiography. RESULTS: In a 36-year-old man, magnetic resonance im aging of the skull and cerebral angiography revealed left intracranial arteriovenous mal...

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Autores principales: Schmidt, D, Agostini, H, Schumacher, M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352052/
https://www.ncbi.nlm.nih.gov/pubmed/20452891
http://dx.doi.org/10.1186/2047-783X-15-2-88
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author Schmidt, D
Agostini, H
Schumacher, M
author_facet Schmidt, D
Agostini, H
Schumacher, M
author_sort Schmidt, D
collection PubMed
description PURPOSE: Follow-up of vascular changes in a patient with congenital retinocephalofacial vascular malformation syndrome. METHODS: MRI and cerebral angiography. RESULTS: In a 36-year-old man, magnetic resonance im aging 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. CONCLUSION: Patients with retinal arteriovenous malformations should be early examined with neuroradiological methods.
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spelling pubmed-33520522012-05-16 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) Schmidt, D Agostini, H Schumacher, M Eur J Med Res Case Report PURPOSE: Follow-up of vascular changes in a patient with congenital retinocephalofacial vascular malformation syndrome. METHODS: MRI and cerebral angiography. RESULTS: In a 36-year-old man, magnetic resonance im aging 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. CONCLUSION: Patients with retinal arteriovenous malformations should be early examined with neuroradiological methods. BioMed Central 2010-02-26 /pmc/articles/PMC3352052/ /pubmed/20452891 http://dx.doi.org/10.1186/2047-783X-15-2-88 Text en Copyright ©2010 I. Holzapfel Publishers
spellingShingle Case Report
Schmidt, D
Agostini, H
Schumacher, M
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)
title 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)
title_full 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)
title_fullStr 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)
title_full_unstemmed 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)
title_short 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)
title_sort 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)
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352052/
https://www.ncbi.nlm.nih.gov/pubmed/20452891
http://dx.doi.org/10.1186/2047-783X-15-2-88
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