Department of Neurosurgery, University of Occupational and Environmental Health, 1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu 807-8555, Japan.
Spine J. 2013 Oct;13(10):e31-8. doi: 10.1016/j.spinee.2013.05.055. Epub 2013 Aug 14.
Germ cell tumors are known to arise in the central nervous system, usually in the intracranial regions. However, primary spinal mixed germ cell tumors are extremely rare.
This is the first reported case of intratumoral hemorrhage because of a primary spinal mixed germ cell tumor consisting of germinoma and immature teratoma in the conus medullaris of an adult patient that presented with rapid changes on magnetic resonance image (MRI). We report this rare case and discuss the clinical manifestations of an intramedullary spinal mixed germ cell tumor in adult.
A case report.
A 42-year-old woman experienced buttock numbness, and a spinal cord tumor was observed on the conus medullaris on MRI. The patient was scheduled for an operation in 1 month, but she developed sudden-onset neurologic deterioration. Rapid progression of the tumor was observed on follow-up MRI. The tumor was removed by emergency surgery and was identified as a primary mixed germinoma and immature teratoma.
The patient received adjuvant chemotherapy and radiotherapy after gross total resection. The neurologic deficit of the patient was relieved, and recurrence of the tumor was not observed 26 months after the surgery.
We present this rare case and emphasize the necessity of precise diagnosis and early treatment of primary spinal germ cell tumor. Close observation on MRI is required after surgery, and adjuvant chemotherapy and radiotherapy should be considered according to the pathologic features.
已知生殖细胞肿瘤起源于中枢神经系统,通常位于颅内区域。然而,原发性脊髓混合生殖细胞瘤极为罕见。
这是首例报告的因位于脊髓圆锥内的生殖细胞瘤和未成熟畸胎瘤混合的原发性脊髓混合生殖细胞瘤而发生肿瘤内出血的病例,该病例为成年患者,其磁共振成像(MRI)上迅速发生变化。我们报告这一罕见病例,并讨论成人脊髓内混合生殖细胞瘤的临床表现。
病例报告。
一名 42 岁女性出现臀部麻木,MRI 显示脊髓圆锥有脊髓肿瘤。患者计划在 1 个月后进行手术,但她突发神经功能恶化。在随访 MRI 上观察到肿瘤迅速进展。通过急诊手术切除肿瘤,病理鉴定为原发性混合生殖细胞瘤和未成熟畸胎瘤。
患者在大体全切除后接受了辅助化疗和放疗。患者的神经功能缺损得到缓解,手术后 26 个月未观察到肿瘤复发。
我们提出这一罕见病例,并强调对原发性脊髓生殖细胞瘤进行精确诊断和早期治疗的必要性。手术后需要密切观察 MRI,并根据病理特征考虑辅助化疗和放疗。