Liechty Peter, Tubbs R Shane, Loukas Marios, Blount Jeffrey P, Wellons John C, Acakpo-Satchivi Leslie, Oakes W Jerry, Grabb Paul A
Pediatric Neurosurgery, Children's Hospital, Birmingham, AL 35233, USA.
Folia Neuropathol. 2007;45(1):23-5.
Accessory nerve meningiomas are exceedingly rare. We present a case of a nine-year-old patient with neurofibromatosis type 2 who had radiologic evidence of spinal cord compression from an upper cervical/foramen magnum lesion. He was asymptomatic from this lesion, but it progressed in size. The tumor was resected and histologic investigation revealed frequent tight whorls and psammoma bodies consistent with meningioma. To the authors' knowledge, this is the first reported spinal accessory nerve meningioma in a pediatric patient.
副神经脑膜瘤极为罕见。我们报告一例9岁的2型神经纤维瘤病患者,其影像学显示上颈椎/枕骨大孔病变导致脊髓受压。该患者对此病变无症状,但病变大小有所进展。肿瘤被切除,组织学检查显示频繁出现紧密的漩涡状结构和砂粒体,符合脑膜瘤表现。据作者所知,这是首例报道的小儿副神经脑膜瘤病例。