先天性视网膜-脑-面血管畸形综合征合并其他先天畸形患者的 27 年随访（Bonnet-Dechaume-Blanc 综合征或 Wyburn-Mason 综合征）。
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).
机构信息
University Freiburg, Augenklinik, Killianstr. 5, 79106 Freiburg, Germany.
出版信息
Eur J Med Res. 2010 Feb 26;15(2):89-91. doi: 10.1186/2047-783x-15-2-88.
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 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.
CONCLUSION
Patients with retinal arteriovenous malformations should be early examined with neuroradiological methods.
目的
随访先天性视网膜-脑-面血管畸形综合征患者的血管变化。
方法
MRI 和脑血管造影。
结果
一名 36 岁男性，头颅 MRI 和脑血管造影显示左侧颅内动静脉畸形。27 年的随访观察发现视网膜和脑动静脉畸形无明显变化。该患者还存在其他先天性缺陷。
结论
视网膜动静脉畸形患者应尽早进行神经影像学检查。
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