Horiuchi H, Yasukawa Y, Akizuki S, Takizawa T, Yamazaki I
Department of Orthopaedic Surgery, Nagano Matsushiro General Hospital, Nagano City, Japan.
J Spinal Disord. 1998 Aug;11(4):359-61.
Neurilemoma of the spinal cord occurred in a mother and daughter. Case 1 was a 75-year-old woman with gait disturbance. Examination revealed weakness of the lower extremities, and magnetic resonance (MR) imaging showed an intradural extramedullary tumor at T12. After laminectomy, the histologic diagnosis was mixed Antoni type A and B neurilemoma. Case 2 was a 48-year-old woman (daughter of case 1). She presented with cervical pain and numbness of both hands. Examination revealed weakened intrinsic muscles of the right hand and paresthesia of the right upper arm. MR imaging showed a giant hourglass-shaped extradural tumor at C2 and C3. The histologic diagnosis was Antoni type A neurilemoma. Only six families with neurilemoma have been reported, including our patients. Gene analysis of such patients may clarify the etiology of neurilemoma.
脊髓神经鞘瘤发生在一对母女身上。病例1是一名75岁女性,有步态障碍。检查发现下肢无力,磁共振成像显示T12水平有硬膜内髓外肿瘤。椎板切除术后,组织学诊断为混合性Antoni A型和B型神经鞘瘤。病例2是一名48岁女性(病例1的女儿)。她表现为颈部疼痛和双手麻木。检查发现右手固有肌肌力减弱,右上臂感觉异常。磁共振成像显示C2和C3水平有一个巨大的沙漏形硬膜外肿瘤。组织学诊断为Antoni A型神经鞘瘤。包括我们的患者在内,仅报道过6个有神经鞘瘤的家族。对此类患者进行基因分析可能会阐明神经鞘瘤的病因。