Fernandes Pedro, do Brito Joaquim Soares, Costa Adília, Monteiro Jacinto
Orthopaedics Department, Centro Hospitalar Lisboa Norte, University Hospital of Santa Maria, Avenida Professor Egas Moniz, 1649-035, Lisbon, Portugal.
Pathology Department, Centro Hospitalar Lisboa Norte, University Hospital of Santa Maria, Lisbon, Portugal.
Eur Spine J. 2018 Jul;27(Suppl 3):477-482. doi: 10.1007/s00586-018-5500-9. Epub 2018 Jan 29.
The anterior elements of the spine, particularly the odontoid processes, are a rare location for osteoblastomas. Pseudomalignant osteoblastomas are themselves rare histologic types and are also extremely rare in this location. Most osteoblastomas are Enneking stage 2 lesions; less frequently, they can be more aggressive with extra-capsular extension (Enneking stage 3). En bloc resection is recommended for aggressive lesions, but the literature is less clear regarding the approach to stage 2 tumors, particularly those with pseudomalignant histologic features.
A 6-year-old male child presented with a type III pathologic fracture of the odontoid. The fracture healed but upon 6-month follow-up CT scanning, an expansile lesion was detected. Surgical biopsy revealed an osteoblastoma which was treated with intralesional excision. Meanwhile, the excised specimen showed histological features of a pseudomalignant osteoblastoma. Despite this diagnosis, no further treatment was undertaken. At a 10-year follow-up, the patient was free from pain and had full range of motion of the cervical spine; no recurrence was detected.
This unique case of odontoid osteoblastoma illustrates that malignant behavior may not be predicted only by the presence of pseudomalignant features on histology.
脊柱的前部结构,尤其是齿状突,是骨母细胞瘤的罕见发病部位。假性恶性骨母细胞瘤本身就是罕见的组织学类型,在这个部位更是极为罕见。大多数骨母细胞瘤为Enneking 2期病变;较少见的情况下,它们可能更具侵袭性,出现包膜外扩展(Enneking 3期)。对于侵袭性病变,建议进行整块切除,但关于2期肿瘤的治疗方法,尤其是具有假性恶性组织学特征的肿瘤,文献报道尚不清楚。
一名6岁男童因齿状突III型病理性骨折就诊。骨折愈合,但在6个月后的随访CT扫描中,发现一个膨胀性病变。手术活检显示为骨母细胞瘤,采用病灶内切除治疗。同时,切除标本显示出假性恶性骨母细胞瘤的组织学特征。尽管有此诊断,但未进行进一步治疗。在10年的随访中,患者无疼痛,颈椎活动范围正常;未检测到复发。
这个独特的齿状突骨母细胞瘤病例表明,恶性行为可能不能仅通过组织学上的假性恶性特征来预测。