Kawagishi J, Suzuki M, Kayama T, Yoshimoto T
Division of Neurosurgery, Tohoku University School of Medicine, Sendai, Japan.
Neurosurgery. 1993 Jun;32(6):1028-30; discussion 1030-1. doi: 10.1227/00006123-199306000-00026.
The authors encountered a rare case of multilobular cavernous angioma arising from the paraventricular region in an infant. Total resection of the angioma, which was 8 cm in diameter, was performed. The patient showed no neurological deficit. Although 22 cases in infants have previously been reported, this is the largest cavernous angioma and it is especially rare because of its multilobular configuration.
作者遇到一例罕见的婴儿脑室旁区域多叶状海绵状血管瘤。对直径8厘米的血管瘤进行了全切。患者无神经功能缺损。尽管此前已报道过22例婴儿病例,但这是最大的海绵状血管瘤,且因其多叶状结构尤为罕见。