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齿突假性恶性骨母细胞瘤

Pseudomalignant osteoblastoma of the odontoid process.

作者信息

Fernandes Pedro, do Brito Joaquim Soares, Costa Adília, Monteiro Jacinto

机构信息

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.

出版信息

Eur Spine J. 2018 Jul;27(Suppl 3):477-482. doi: 10.1007/s00586-018-5500-9. Epub 2018 Jan 29.

DOI:10.1007/s00586-018-5500-9
PMID:29380146
Abstract

INTRODUCTION

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.

CASE REPORT

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.

CONCLUSION

This unique case of odontoid osteoblastoma illustrates that malignant behavior may not be predicted only by the presence of pseudomalignant features on histology.

摘要

引言

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。

病例报告

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。

结论

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。

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Pseudomalignant osteoblastoma of the odontoid process.齿突假性恶性骨母细胞瘤
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Osteoblastoma of the odontoid process.齿突骨母细胞瘤
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本文引用的文献

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Benign Bone-Forming Tumors: Approach to Diagnosis and Current Understanding of Pathogenesis.良性骨形成肿瘤:诊断方法与发病机制的当前认识
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Staging and treatment of osteoblastoma in the mobile spine: a review of 51 cases.脊柱活动部骨母细胞瘤的分期和治疗:51 例回顾。
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In brief: classifications in brief: enneking classification: benign and malignant tumors of the musculoskeletal system.简而言之:简要分类:恩宁克分类法:肌肉骨骼系统的良性和恶性肿瘤。
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Aggressive "benign" primary spine neoplasms: osteoblastoma, aneurysmal bone cyst, and giant cell tumor.侵袭性“良性”原发性脊柱肿瘤:骨母细胞瘤、动脉瘤样骨囊肿和巨细胞瘤。
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Osteoid osteoma and osteoblastoma of the spine.脊柱骨样骨瘤和成骨细胞瘤
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[Osteoblastoma of the dens axis in a 14-year-old boy. A case report].[一名14岁男孩枢椎骨母细胞瘤。病例报告]
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Osteoid osteomas and osteoblastomas of the occipitocervical junction.枕颈交界区骨样骨瘤和成骨细胞瘤
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