Bhattacharya J J, Luo C B, Suh D C, Alvarez H, Rodesch G, Lasjaunias P
Institute of Neurological Sciences, Southern General Hospital; Glasgow, UK -
Interv Neuroradiol. 2001 Mar 30;7(1):5-17. doi: 10.1177/159101990100700101. Epub 2001 May 15.
The diagnosis of Bonnet-Dechaume-Blanc or Wyburn-Mason syndrome encompasses a spectrum of phenotypic expression. Features of the syndrome as originally described, and common to all, include arteriovenous malformations of the brain and orbit (with retinal and/or retrobulbar lesions). A portion of these patients manifest the complete expression of the disease with additional high-flow arteriovenous malformations of the maxillofacial or mandibular regions. These present the distinct and additional risks of lifethreatening epistaxis or gingival haemorrhage. We suggest new diagnostic criteria for the syndrome. Applying insights from modern developmental biology to our series of 15 patients (the largest to date), together with a review of the literature, we have recognised metameric patterns of involvement in what we believe to be a disease of the neural crest or adjacent cephalic mesoderm. This allows us to propose a new rational classification reflecting the putative, underlying disorder and to suggest a new name: Cerebrofacial Arteriovenous Metameric Syndrome (CAMS).
邦尼特-德肖姆-布朗综合征或怀伯恩-梅森综合征的诊断涵盖一系列表型表现。该综合征最初描述的、且所有病例共有的特征包括脑和眼眶的动静脉畸形(伴有视网膜和/或球后病变)。这些患者中有一部分表现出疾病的完整症状,还伴有颌面部或下颌区域的高流量动静脉畸形。这些情况存在危及生命的鼻出血或牙龈出血等独特且额外的风险。我们提出了该综合征的新诊断标准。将现代发育生物学的见解应用于我们的15例患者系列(迄今最大的系列),并结合文献综述,我们在我们认为是神经嵴或相邻头部中胚层疾病中识别出了节段性受累模式。这使我们能够提出一种反映假定潜在疾病的新的合理分类,并建议一个新名称:脑颜面动静脉节段性综合征(CAMS)。