Algoet Michiel, Van Dyck-Lippens Pieter Jan, Casselman Jan, Sirimsi Sabriya, Fletcher Christophe D M, Van Den Berghe Ivo, Vanopdenbosch Ludo, De Muynck Stijn, Vantomme Nikolaas
University of Leuven, Leuven, Belgium; Department of Neurosurgery, AZ Sint-Jan Brugge-Oostende, Brugge, Belgium.
Department of Neurosurgery, University Hospitals Leuven, Leuven, Belgium; Department of Neurosurgery, AZ Sint-Jan Brugge-Oostende, Brugge, Belgium.
World Neurosurg. 2019 Jun;126:428-433. doi: 10.1016/j.wneu.2019.02.202. Epub 2019 Mar 12.
Cerebral cavernous malformations of the intracanalicular optic nerve are extremely rare lesions. Only a few case reports and 1 case series have been published. We report an additional case with atypical imaging and review the existing literature with attention to time to surgery and imaging characteristics.
In a 38-year-old man with progressive visual field deficit, a lesion compressing the left optic nerve in the optic canal was diagnosed. On magnetic resonance imaging, this lesion had a homogeneous signal and was tentatively diagnosed as a meningioma. A left frontolateral craniotomy with extradural skull base approach with neuronavigation was performed for resection and definitive diagnosis of the lesion. Pathologic examination showed a lesion most consistent with a cavernous hemangioma. Follow-up magnetic resonance imaging at 6 months showed no remaining tissue or recurrence. Clinically, there was subjective and objective improvement of sight.
A cerebral cavernous malformation should always be in the differential diagnosis of a lesion causing an optic neuropathy with visual acuity loss and visual field defect. Clinical presentation of an optic neuropathy requires medical imaging; magnetic resonance imaging is the modality of choice in the diagnosis of these lesions. The treatment of cerebral cavernous malformation is gross total resection.
管内段视神经的脑海绵状畸形是极其罕见的病变。仅有少数病例报告和1个病例系列发表。我们报告1例具有非典型影像学表现的病例,并回顾现有文献,重点关注手术时机和影像学特征。
一名38岁男性,出现进行性视野缺损,诊断为视神经管内压迫左侧视神经的病变。磁共振成像显示该病变信号均匀,初步诊断为脑膜瘤。采用左侧额颞开颅、硬膜外颅底入路并结合神经导航进行病变切除及明确诊断。病理检查显示病变最符合海绵状血管瘤。6个月后的随访磁共振成像显示无残留组织或复发。临床上,视力有主观和客观改善。
脑海绵状畸形应始终列入导致视力丧失和视野缺损的视神经病变的鉴别诊断中。视神经病变的临床表现需要进行医学成像检查;磁共振成像是诊断这些病变的首选方式。脑海绵状畸形的治疗是全切术。