Kritikos Michael E, Oselkin Martin, Sharma Nikhil, Gopal Pallavi P, Bigelow Douglas C, Grady Sean, Hurst Robert W, Pukenas Bryan A, Choudhri Omar, Kung David
Neurosurgery, Hospital of the University of Pennsylvania, Philadelphia, USA.
Neuroradiology, Hospital of the University of Pennsylvania, Philadelphia, USA.
Cureus. 2018 Jun 27;10(6):e2890. doi: 10.7759/cureus.2890.
Intracranial dural arteriovenous fistulae (DAVF) are rare vascular malformations. They are generally considered to be acquired lesions, often attributed to dural sinus thrombosis and intracranial venous hypertension. The authors encountered a case of DAVF associated with an octreotide-positive vestibular schwannoma. A 46-year-old female had symptoms of right ear congestion accompanied by pulsatile tinnitus and mild hearing loss. Magnetic resonance imaging (MRI) identified a lobulated mass centered at the cerebellopontine angle. Preoperatively, on cerebral angiography, there was an incidental discovery of a DAVF in the right posterior fossa. The decision was made to proceed with resection of the tumor in a staged fashion. Her latest follow-up MRI showed no evidence of recurrent tumor. This is the second reported case of DAVF associated with an intracranial schwannoma. Findings are discussed along with a thorough review of the literature. This case, combined with the data from the literature review, led us to believe that tumor-related angiogenesis might contribute to DAVF formation.
颅内硬脑膜动静脉瘘(DAVF)是一种罕见的血管畸形。它们通常被认为是后天性病变,常归因于硬脑膜窦血栓形成和颅内静脉高压。作者遇到了一例与奥曲肽阳性前庭神经鞘瘤相关的DAVF。一名46岁女性有右耳闷胀症状,伴有搏动性耳鸣和轻度听力损失。磁共振成像(MRI)发现一个以桥小脑角为中心的分叶状肿块。术前,脑血管造影偶然发现右后颅窝有一个DAVF。决定分阶段进行肿瘤切除。她最近的随访MRI显示没有肿瘤复发的迹象。这是第二例报道的与颅内神经鞘瘤相关的DAVF。结合文献进行了详细讨论。该病例与文献综述的数据一起,使我们相信肿瘤相关的血管生成可能促成DAVF的形成。