小儿颈椎骨样骨瘤和成骨细胞瘤:文献分析和4例手术病例的经验。

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY
Alexandru Szathmari, Laryssa Crystinne Azevedo Almeida, Pierre-Aurélien Beuriat, Camilla de Laurentis, Matthieu Vinchon, Federico Di Rocco
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引用次数: 0

摘要

背景与目的:骨样骨瘤(Oo)和成骨细胞瘤(Ob)是一种罕见的原发性骨肿瘤,发病率较高,多发生在20岁左右。治疗可以是保守的,但在脊柱位置的情况下,切除手术是非常重要的,但可能具有挑战性。材料和方法:我们报告四例小儿Oo和Ob在我单位管理,在颈椎水平的不同位置。所有4例患者均有持续和进行性颈部疼痛的共同主诉,2例报告夜间疼痛加重,3例接受非甾体抗炎药治疗,但无明显反应。所有病例的影像学检查均发现颈椎骨源病变:2例在椎弓根椎板复合体,1例在椎板,1例在C2椎体和齿状突水平。通过比较资料和讨论案例,进行了全面的文献综述。结果:3例患者经后路手术切除,1例经口手术切除。在所有病例中,坚硬的颈圈在成型下确保了术后的稳定性。对照影像学检查显示病灶切除满意。组织学上,3例为成骨细胞瘤,1例为骨样骨瘤。对照影像学研究显示病灶切除满意,后期骨重建良好。最终,没有一例患者表现出需要固定治疗的晚期不稳定。平均随访时间36(16-63)个月。没有复发,也没有需要固定的晚期不稳定。结论:小儿颈椎类骨性骨瘤和成骨细胞瘤的治疗应寻求完全切除。在有继发性不稳定风险的区域,保留囊韧带结构和临时骨科固定可以在不需要固定的情况下实现骨再生。建议延长随访时间,特别是在非常年幼的儿童中,以避免后期不稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Osteoid osteoma and osteoblastoma of the cervical spine in the pediatric population: analysis of the literature and experience with four operated cases.

Background and aim: Osteoid osteoma (Oo) and osteoblastoma (Ob) are rare primary bone tumors with a higher prevalence in the second decade of life. Treatment can be conservative, but in cases of spinal location, resective surgery is of great importance but may be challenging.

Material and methods: We report four pediatric cases of Oo and Ob managed in our unit, with different locations at the level of the cervical spine. All four patients had a common complaint of persistent and progressive neck pain, two reported worsening pain at night, and three underwent NSAID treatment attempts without significant response. The radiological examination revealed a lesion of bone origin in the cervical spine in all cases: two at the pediculolaminar complex, one at the laminar, and one at the level of the C2 body and odontoid. A comprehensive literature review was carried out by comparing the data and a discussion of the cases.

Results: A complete surgical resection was performed by a posterior approach in three patients and a transoral in one. A hard neck collar under molding ensured postoperative stability in all cases. Control imaging studies demonstrated satisfactory lesion resection. Histologically, three cases were an osteoblastoma and one an osteoid osteoma. Control imaging studies demonstrated satisfactory lesion resection with good late bone reconstruction. Ultimately, none showed late instability requiring fixation. The mean follow-up time is 36 (16-63) months. None had a recurrence nor late instability requiring fixation.

Conclusion: Treatment of pediatric cervical spine of osteoid osteoma and osteoblastoma should seek a complete resection. In regions with a risk for secondary instability, the preservation of capsule-ligamental structures and temporary orthopedic immobilization can allow bone regeneration with no need for fixation. Extended follow-up is recommended especially in very young children to avoid late instability.

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来源期刊
Child's Nervous System
Child's Nervous System 医学-临床神经学
CiteScore
3.00
自引率
7.10%
发文量
322
审稿时长
3 months
期刊介绍: The journal has been expanded to encompass all aspects of pediatric neurosciences concerning the developmental and acquired abnormalities of the nervous system and its coverings, functional disorders, epilepsy, spasticity, basic and clinical neuro-oncology, rehabilitation and trauma. Global pediatric neurosurgery is an additional field of interest that will be considered for publication in the journal.
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