Pediatric de novo cerebral AVM: report of two cases and review of literature

被引:31
|
作者
Yeo, Jared J. Y. [1 ]
Low, Sharon Y. Y. [2 ]
Seow, Wan Tew [3 ]
Low, David C. Y. [3 ]
机构
[1] Univ New S Wales, Fac Med, Sydney, NSW 2052, Australia
[2] Natl Neurosci Inst Singapore, Dept Neurosurg, Singapore 308433, Singapore
[3] KK Womens & Childrens Hosp, Neurosurg Serv, Singapore, Singapore
关键词
Arterio-venous malformation; Cerebral venous malformation; ENDOTHELIAL GROWTH-FACTOR; ARTERIOVENOUS-MALFORMATION; CHILD;
D O I
10.1007/s00381-014-2609-y
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cerebral arteriovenous malformation (AVM) is traditionally thought of as a congenital diagnosis. In recent years, there has been infrequent reports of this neurovascular condition presenting as de novo entities. The authors report two cases of pediatric patients who present with de novo cerebral AVMs. In both cases, the patients had magnetic resonance imaging (MRI) of the brain done as part of the work-up for first-onset seizures. At that point in time, the scans were unremarkable. After a latent period of approximately 6 and 9 years respectively, a repeated MRI brain scan showed evidence of de novo AVM for each patient. Both patients did not have radiological evidence of cerebral AVM during their first presentation of seizures. However, a repeated MRI brain scan after a period of 6 and 9 years demonstrated new findings of cerebral AVM for each patient. Currently, the disease of cerebral de novo AVM remain as an ambiguous condition that is poorly understood. With the advances in molecular diagnostics, there are possibilities of exploring biochemical profiles for better understanding of the origin of cerebral AVMs. However, in the meantime, owing to the unpredictable nature of cerebral AVMs, clinicians should have increased awareness of this unique condition. This is especially important, as definitive treatment is available to prevent devastating neurological sequelae from cerebral AVM rupture.
引用
收藏
页码:609 / 614
页数:6
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