Konishi Y, Hieshima G B, Hara M, Yoshino K, Yano K, Takeuchi K
Department of Neurosurgery, Kyorin University School of Medicine, Tokyo, Japan.
Neurosurgery. 1990 Jul;27(1):120-6. doi: 10.1097/00006123-199007000-00018.
The case of a 2-month-old boy with a congenital fistula of the dural carotid-cavernous sinus is presented. This is a rare vascular anomaly in infancy, and it may cause acute changes in vision. The child was initially followed up for 1 year to see if spontaneous thrombosis would occur. The symptoms persisted, however, and intravascular surgery using platinum coils was performed for closure. After treatment, the symptoms completely resolved. Literature pertaining to this anomaly has been reviewed with particular emphasis on dural fistulas of the cavernous, transverse, sigmoid, and straight sinuses in infancy.
本文报道了一例2个月大患有先天性硬脑膜颈动脉海绵窦瘘的男婴病例。这是一种罕见的婴儿期血管异常,可能导致视力急性改变。该患儿最初随访1年,观察是否会发生自发性血栓形成。然而,症状持续存在,遂采用铂圈进行血管内手术以封闭瘘口。治疗后,症状完全缓解。本文回顾了有关该异常的文献,特别强调了婴儿期海绵窦、横窦、乙状窦和直窦的硬脑膜瘘。