Osteoblastoma of the orbit: A rare case report and review of the literature

Andrew C. Jenzer , Victoria Wickenheisser , Diana Marcella Cardona , David B. Powers
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引用次数: 0

Abstract

Osteoblastoma is a benign tumor of bone representing less than 1% of all primary bone tumors [1]. Osteoblastomas are primarily reported in long bones and the spinal column, with craniofacial cases representing about 15% of the literature (Meli et al., 2008; Kroon and Schurmans, 1990) [1,2]. Osteoblastoma with orbital involvement is exceedingly rare, with less than twenty-five documented cases (Akhaddar et al., 2004; Meli et al., 2008; Bilkay et al., 2004; Hafidi and Daoudi, 2013) [3,1,4,5]. The mainstay of treatment for osteoblastoma is surgical excision with consideration for resection depending on the lesion, size, location, involved structures, and clinical presentation. The authors present a case of an orbital osteoblastoma presenting with globe subluxation in a pediatric patient.

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眼眶成骨细胞瘤:一例罕见病例报告及文献复习
成骨细胞瘤是一种骨良性肿瘤,在所有原发性骨肿瘤中所占比例不到1%[1]。成骨细胞瘤主要报道于长骨和脊柱,颅面病例约占文献的15% (Meli et al., 2008;Kroon and Schurmans, 1990)[1,2]。眼眶受累的成骨细胞瘤极为罕见,文献记载的病例少于25例(Akhaddar et al., 2004;Meli et al., 2008;Bilkay et al., 2004;Hafidi and Daoudi, 2013)[3,1,4,5]。成骨细胞瘤的主要治疗方法是手术切除,根据病变、大小、位置、受累结构和临床表现考虑切除。作者提出了一个病例眼眶成骨细胞瘤提出全球半脱位的儿科患者。
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来源期刊
Oral and Maxillofacial Surgery Cases
Oral and Maxillofacial Surgery Cases Medicine-Otorhinolaryngology
CiteScore
0.60
自引率
0.00%
发文量
43
审稿时长
69 days
期刊介绍: Oral and Maxillofacial Surgery Cases is a surgical journal dedicated to publishing case reports and case series only which must be original, educational, rare conditions or findings, or clinically interesting to an international audience of surgeons and clinicians. Case series can be prospective or retrospective and examine the outcomes of management or mechanisms in more than one patient. Case reports may include new or modified methodology and treatment, uncommon findings, and mechanisms. All case reports and case series will be peer reviewed for acceptance for publication in the Journal.
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