Liu Shuzhong, Zhou Xi, Song An, Huo Zhen, Wang Yipeng, Liu Yong
Department of Orthopaedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences.
Department of Endocrinology, Key Laboratory of Endocrinology, National Health and Family Planning Commission, Peking Union Medical College Hospital, Chinese Academy of Medical Science & Peking Union Medical College.
Medicine (Baltimore). 2020 Jan;99(5):e18643. doi: 10.1097/MD.0000000000018643.
Metastatic mesenchymal chondrosarcoma of the spine is a highly unusual disease without standard curative managements yet. The objective of this case report is to present a very rare case of metastatic chondrosarcoma to the spine successfully operated by surgical treatment. The management of these unique cases has yet to be well-documented.
A 34-year-old woman presented with a 4-month history of continuous and progressive back pain and a 1-month history of radiating pain of bilateral lower extremities. The patient, who had been diagnosed of mesenchymal chondrosarcoma of maxillary sinus for 3 years, received surgical treatment of palliative endoscopic-assisted total left maxillary resection via mini Caldwell-Luc approach, and palliative enlarged resection due to the progress of residual lesions, followed by no adjuvant therapy. Multiple lytic, expanding lesions of the spine and paraspinal region with severe epidural spinal cord compression was identified.
CT, MRI and bone scan of spine showed spinal cord compression secondary to the epidural component of the metastatic lesions. Post-operative pathology confirmed the diagnosis of metastatic spinal mesenchymal chondrosarcomas.
The patient underwent posterior spinal canal decompression, resection of T12 and L3 lesions, internal fixation of T11-L5 pedicles, and cement augmentation of T12 and L3.
The patient's neurological deficits improved significantly after the surgery, and the postoperative period was uneventful at the 1-year follow-up visit. There were no complications associated with the spinal surgery during the follow-up period.
Metastatic spinal mesenchymal chondrosarcoma, although rare, should be part of the differential diagnosis when the patient presents with back pain and radiculopathy. We recommend the posterior approach for spinal decompression and total resection of the metastatic chondrosarcoma when the tumor has caused neurological deficits or other severe symptoms. Osteoplasty by cement augmentation is also a good choice for surgical treatment in some patients.
脊柱转移性间叶性软骨肉瘤是一种极为罕见的疾病,目前尚无标准的治愈性治疗方法。本病例报告的目的是呈现一例非常罕见的脊柱转移性软骨肉瘤病例,该病例成功接受了手术治疗。这些特殊病例的治疗方法尚未得到充分记录。
一名34岁女性,有4个月持续进行性背痛病史及1个月双侧下肢放射性疼痛病史。该患者3年前被诊断为上颌窦间叶性软骨肉瘤,接受了经改良柯氏入路的姑息性内镜辅助全左侧上颌骨切除术,因残留病变进展又进行了姑息性扩大切除术,术后未接受辅助治疗。发现脊柱和椎旁区域有多个溶骨性、膨胀性病变,并伴有严重的硬膜外脊髓压迫。
脊柱CT、MRI及骨扫描显示转移性病变的硬膜外成分导致脊髓受压。术后病理证实为脊柱转移性间叶性软骨肉瘤。
患者接受了后路椎管减压、T12和L3病变切除、T11-L5椎弓根内固定以及T12和L3椎体骨水泥强化。
术后患者神经功能缺损明显改善,1年随访期内术后情况平稳。随访期间未发生与脊柱手术相关的并发症。
脊柱转移性间叶性软骨肉瘤虽然罕见,但当患者出现背痛和神经根病时,应作为鉴别诊断的一部分。当肿瘤导致神经功能缺损或其他严重症状时,我们建议采用后路进行脊柱减压及转移性软骨肉瘤全切术。对于部分患者,椎体骨水泥强化成形术也是一种不错的手术治疗选择。