*Department of Neurosurgery, †Department of Neuropathology, Institute of Pathology, and ‡Department of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
Spine (Phila Pa 1976). 2013 Dec 15;38(26):E1709-13. doi: 10.1097/BRS.0000000000000029.
A case report.
To demonstrate 2 cases of delayed distant spinal metastasis from a thymoma with comprehensive immunohisto-chemical analysis.
Thymoma is a rare slow-growing cancer arising in the mediastinum. Thymomas usually grow invasively into surrounding structures. Distal spinal metastasis is uncommon. To date, only 4 cases with histological verification have been described.
Patient 1: A 42-year-old female complained about back pain for 4 years. She underwent gross-total resection of a type B2 thymoma 8 years earlier without adjuvant therapy. Neurological examination revealed no deficits. Magnetic resonance imaging demonstrated an intraspinal extradural tumor at the level of L4-S1 with infiltration of vertebral body L5. A nearly total resection was performed via a partial L4 and L5 hemilaminectomy.Patient 2: A 62-year-old female was referred with segmental thoracic pain. She underwent a total of 6 surgical procedures for resection of a thymic carcinoma during a period of 13 years with a subsequently local radiation therapy and various chemotherapy cycles. Magnetic resonance imaging revealed an intraspinal extradural tumor at the level of T9-T10 with infiltration of vertebral body T9-T10. A gross-total tumor resection was performed via a costotransversectomy and facetectomy T9-T10.
Patient 1: The tumor cells were strongly positive for AE1/3- and CK5/14-specific antibodies. Most of the immature T-cells expressed CD3. CD1a, CD5, and TdT expression was observed in a smaller portion. The findings were consistent with the diagnosis of a spinal metastasis of the known type B2 thymoma.Patient 2: The tumor cells were CK5/14 and CK19/20 positive. Only the infiltrating lymphocytes were labeled with CD3-specific antibodies. Histopathological findings revealed a metastasis of a previously resected well-differentiated thymus carcinoma.
We recommend surgical resection because metastasis of thymoma may infiltrate nerve roots and compress the spinal cord. A multidisciplinary approach is required to manage long-term sequelae.
病例报告。
通过全面的免疫组织化学分析,展示 2 例胸腺瘤引起的延迟性远隔脊柱转移病例。
胸腺瘤是一种罕见的生长缓慢的纵隔恶性肿瘤。胸腺瘤通常会侵袭性地生长到周围结构中。远处脊柱转移并不常见。迄今为止,仅描述了 4 例经组织学证实的病例。
患者 1:一名 42 岁女性,背痛 4 年。8 年前,她因 B2 型胸腺瘤接受了大体全切除手术,未行辅助治疗。神经学检查无明显缺陷。磁共振成像显示 L4-S1 水平椎管内硬膜外肿瘤,L5 椎体浸润。通过部分 L4 和 L5 半椎板切除术进行了近全切除。患者 2:一名 62 岁女性因节段性胸背痛就诊。她在 13 年内共进行了 6 次胸腺癌切除术,随后进行局部放疗和各种化疗周期。磁共振成像显示 T9-T10 水平椎管内硬膜外肿瘤,T9-T10 椎体浸润。通过 T9-T10 经肋横突切除和关节突切除进行了大体全肿瘤切除。
患者 1:肿瘤细胞对 AE1/3-和 CK5/14 特异性抗体呈强阳性。大多数不成熟 T 细胞表达 CD3。CD1a、CD5 和 TdT 的表达量较小。这些发现与已知的 B2 型胸腺瘤脊柱转移的诊断相符。患者 2:肿瘤细胞 CK5/14 和 CK19/20 阳性。只有浸润淋巴细胞被 CD3 特异性抗体标记。组织病理学发现为先前切除的分化良好的胸腺癌转移。
我们建议进行手术切除,因为胸腺瘤转移可能会浸润神经根并压迫脊髓。需要多学科方法来管理长期的后遗症。