Tanaka K, Yonekawa Y, Miyake H
Department of Neurosurgery, National Cardiovascular Center, Suita, Osaka, Japan.
Surg Neurol. 1991 Sep;36(3):221-5. doi: 10.1016/0090-3019(91)90117-r.
We present an unusual case involving intracranial arteriovenous malformations in the anterior cranial fossa located symmetrically on both sides. A mixed pial and dural arteriovenous malformation, the nidus of which was localized in the brain parenchyma, was found on the right side and a pure dural arteriovenous malformation on the left side. Our case is felt to support the hypothesis of a congenital origin for dural arteriovenous malformation in the anterior cranial fossa, because the dural arteriovenous malformation coexisted with the mixed pial and dural arteriovenous malformation, which can be attributed to a disturbance of normal embryonic development.
我们报告了一例罕见病例,涉及前颅窝双侧对称分布的颅内动静脉畸形。右侧发现一个软脑膜和硬脑膜混合型动静脉畸形,其病灶位于脑实质内,左侧为单纯硬脑膜动静脉畸形。我们的病例被认为支持前颅窝硬脑膜动静脉畸形先天性起源的假说,因为硬脑膜动静脉畸形与软脑膜和硬脑膜混合型动静脉畸形共存,这可归因于正常胚胎发育的紊乱。