Kitagawa Ryo, Murakami Hideki, Kato Satoshi, Nakada Mitsutoshi, Demura Satoru, Tsuchiya Hiroyuki
Department of Orthopaedic Surgery, Kanazawa University School of Medicine, Kanazawa, Japan.
Department of Orthopaedic Surgery, Kanazawa University School of Medicine, Kanazawa, Japan.
World Neurosurg. 2016 Jun;90:698.e1-698.e5. doi: 10.1016/j.wneu.2015.09.102. Epub 2015 Oct 13.
Paragangliomas are neuroendocrine tumors that originate from autonomic nervous system-associated paraganglia and are rare tumors accounting for only 0.3% of all neoplasms. Malignant paragangliomas frequently spread to the skeleton. The authors present a case of malignant paraganglioma with bone metastases to the spine and cranium, as well as excellent local control achieved with en bloc tumor resection and reconstruction using frozen tumor-bearing bone for the sites of the metastases.
The patient was a 61-year-old woman who underwent retroperitoneal paraganglioma resection 12 years previously. Nine years after the primary surgery, she began to experience back pain. Magnetic resonance imaging revealed an isolated metastasis in T6, and the following evaluation detected another metastasis in the left temporal bone. We performed curative surgeries for the metastases, including total en bloc spondylectomy of T6, partial craniectomy for the cranial metastasis, and spinal and cranial reconstruction using frozen tumor-bearing bone for the sites of the metastases. At the 24-month follow-up examination, bone fusion was achieved between the frozen bone and the adjacent healthy bone in the spine and cranium. At 36 months postoperatively, an asymptomatic metastatic lesion was found in the pelvis. Nevertheless, no local recurrences at the surgical sites were detected. Her quality of life and performance in activities of daily living were well preserved. To the author's knowledge, this is the first report to present a case of cranioplasty achieved using a liquid nitrogen frozen, tumor-bearing autologous bone flap in a single-stage operation.
副神经节瘤是起源于自主神经系统相关副神经节的神经内分泌肿瘤,是罕见肿瘤,仅占所有肿瘤的0.3%。恶性副神经节瘤常转移至骨骼。作者报告1例恶性副神经节瘤发生脊柱和颅骨骨转移的病例,以及通过整块肿瘤切除并用冷冻的含瘤骨对转移部位进行重建实现了良好的局部控制。
患者为一名61岁女性,12年前接受了腹膜后副神经节瘤切除术。初次手术后9年,她开始出现背痛。磁共振成像显示T6有孤立转移灶,随后的评估在左侧颞骨发现了另一处转移灶。我们对转移灶进行了根治性手术,包括T6椎体整块切除术、颅骨转移灶的部分颅骨切除术,并用冷冻的含瘤骨对转移部位进行脊柱和颅骨重建。在24个月的随访检查中,脊柱和颅骨的冷冻骨与相邻健康骨之间实现了骨融合。术后36个月,在骨盆发现了一个无症状转移灶。然而,手术部位未检测到局部复发。她的生活质量和日常生活活动能力得到了很好的保留。据作者所知,这是首例报告单阶段手术使用液氮冷冻的含瘤自体骨瓣进行颅骨成形术的病例。