地诺单抗治疗在复发性眼眶巨细胞骨肿瘤中的作用

IF 1.2 4区 医学 Q3 OPHTHALMOLOGY
Arjav Gupta, Bruce Colwell, David B Clarke, Emad A Massoud, Sidney Croul, Ahsen Hussain
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引用次数: 0

摘要

骨巨细胞瘤(GCTB)是一种罕见的原发性骨肿瘤,约占所有原发性骨肿瘤的 5%。大多数骨巨细胞瘤发生在长骨的骨骺,只有 2% 的骨巨细胞瘤累及颅骨。近年来,核因子 Kappa 配体受体激活剂单克隆抗体地诺单抗已被证明是治疗 GCTB 的一种有前途的选择;然而,这是一个不断发展的领域。我们报告了一例 57 岁女性的病例,她患有罕见的右眼眶和鼻窦 GCTB,最初被认为是动脉瘤性骨囊肿。她的症状包括眼球突出、间歇性视力模糊、鼻窦充血和额部头痛。切除肿瘤后,肿瘤在 18 个月内复发。再次切除后,诊断为 GCTB。患者开始接受地诺单抗治疗,在随后的两年中肿瘤没有生长,随访时症状和临床体征均稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Role of Denosumab Treatment in Recurrent Giant Cell Bone Tumor of the Orbit.

Giant cell tumor of the bone (GCTB) is a rare primary bone neoplasm, representing about 5% of all primary bone tumors. Most GCTBs are found in the epiphysis of long bones, with only 2% of GCTBs involving the skull. In recent years, the receptor activator of nuclear factor Kappa ligand monoclonal antibody denosumab has been demonstrated as a promising therapeutic option for GCTB; however, this is an evolving field. We present a case of a 57-year-old female with a rare GCTB in the right orbit and sinuses, originally thought to be an aneurysmal bone cyst. Her symptoms included proptosis, intermittent blurry vision, sinus congestion, and frontal headaches. After excision, the tumor recurred within 18 months. Upon repeat excision, a diagnosis of GCTB was made. The patient started denosumab therapy and had no tumor growth over the ensuing 2 years, with stability of symptoms and clinical signs on follow-up.

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来源期刊
CiteScore
2.50
自引率
10.00%
发文量
322
审稿时长
3-8 weeks
期刊介绍: Ophthalmic Plastic and Reconstructive Surgery features original articles and reviews on topics such as ptosis, eyelid reconstruction, orbital diagnosis and surgery, lacrimal problems, and eyelid malposition. Update reports on diagnostic techniques, surgical equipment and instrumentation, and medical therapies are included, as well as detailed analyses of recent research findings and their clinical applications.
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