Tang Shenghui, Zuo Junhua, Zhang Haonan, Wu Zhanglin, Liang Biru
Department of Orthopaedics, the Fifth Affiliated Hospital, Southern Medical University, Guangzhou, China.
Department of Gastroenterology, the Fifth Affiliated Hospital, Southern Medical University, Guangzhou, China.
World Neurosurg. 2020 Aug;140:320-324. doi: 10.1016/j.wneu.2020.05.067. Epub 2020 May 16.
Metastatic malignant melanoma of the spine is rare, while the spinal metastatic melanoma with unknown primary lesions presenting as radiculopathy is even rarer. Summarizing and analyzing this disease can provide insight into disease development and allow optimization of clinical management.
A 55-year-old male patient was admitted to our institution presenting with lower back pain that had persisted for 3 years. It was aggravated, with radiating pain in bilateral lower extremities lasting 2 weeks. Neurologic examination revealed bilateral L5 motor deficit with paresis. Radiologic findings showed an irregularly destructive lesion of the L5 vertebral body, and the lesion extended dorsally, obstructing the spinal canal. The patient underwent complete resection of the L5 vertebral tumor with titanium mesh implantation and posterior fusion and instrumentation from L3-S2. The pathologic diagnosis after surgery was malignant melanoma. No obvious primary lesion was detected anywhere on the skin surface, mucosa, and retina. A postoperative positron emission tomography-computed tomography scan of the whole body displayed no abnormal uptake in other parts of the body. However, the patient didn't receive any chemotherapy or radiotherapy. Five months after operation, the tumor recurred and metastasis was detected in other sites.
Although spinal metastatic melanoma with unknown primary lesions presenting as radiculopathy is rare, effective management and treatment of these patients remains an important challenge for surgeons. Surgical resection can alleviate patients' chief complaints and improve their quality of life. However, it may not prolong the survival period and improve the prognosis. Postoperative radiotherapy and/or chemotherapy may be needed.
脊柱转移性恶性黑色素瘤较为罕见,而以神经根病为表现的原发性病灶不明的脊柱转移性黑色素瘤更为罕见。总结和分析这种疾病有助于深入了解疾病发展过程,并优化临床管理。
一名55岁男性患者因下背部疼痛持续3年入院。疼痛加重,伴有双侧下肢放射性疼痛,持续2周。神经系统检查显示双侧L5运动功能障碍伴轻瘫。影像学检查发现L5椎体有不规则破坏性病变,病变向背侧延伸,阻塞椎管。患者接受了L5椎体肿瘤全切术,植入钛网,并进行了L3-S2的后路融合及内固定术。术后病理诊断为恶性黑色素瘤。在皮肤表面、黏膜及视网膜均未发现明显的原发性病灶。术后全身正电子发射断层扫描-计算机断层扫描显示身体其他部位无异常摄取。然而,患者未接受任何化疗或放疗。术后5个月,肿瘤复发并在其他部位出现转移。
尽管以神经根病为表现的原发性病灶不明的脊柱转移性黑色素瘤罕见,但对这些患者进行有效的管理和治疗仍是外科医生面临的一项重要挑战。手术切除可缓解患者的主要症状,提高生活质量。然而,手术可能无法延长生存期和改善预后。术后可能需要放疗和/或化疗。