King D, Goodman J, Hawk T, Boles E T, Sayers M P
Arch Surg. 1975 Aug;110(8):888-91. doi: 10.1001/archsurg.1975.01360140032006.
A "dumbbell" neuroblastoma is a malignant neoplasm usually primary in the mediastinum or retroperitoneum with posterior extension through an intervertebral foramen to additional tumor within the spinal canal. Neurologic deficits are found in almost all cases. Nineteen patients with such tumors were reviewed with respect to diagnosis, management, and results. Treatment consisted of prompt laminectomy with total or subtotal excision of the extradural tumor. The primary tumor in the mediastinum or retroperitoneal area was removed at a second stage. All patients received postoperative radiation therapy. Eleven of the 17 patients observed more than two years are free of disease, a cure rate much higher than the overall experience with neuroblastoma. Substantial recovery of neurologic function occurred in most, but kyphoscoliotic deformities were a disturbingly frequent late complication.
“哑铃型”神经母细胞瘤是一种恶性肿瘤,通常原发于纵隔或腹膜后,肿瘤向后通过椎间孔延伸至椎管内形成额外的肿瘤。几乎所有病例均有神经功能缺损。对19例此类肿瘤患者的诊断、治疗及结果进行了回顾。治疗包括立即行椎板切除术,完全或次全切除硬膜外肿瘤。纵隔或腹膜后区域的原发肿瘤在第二阶段切除。所有患者术后均接受放疗。17例观察超过两年的患者中有11例无疾病,治愈率远高于神经母细胞瘤的总体治疗经验。大多数患者神经功能有显著恢复,但脊柱后凸侧弯畸形是一种令人不安的常见晚期并发症。