地诺单抗治疗侵袭性成骨细胞瘤伴继发性动脉瘤性骨囊肿。

IF 0.9 Q4 ONCOLOGY Rare Tumors Pub Date : 2021-08-29 eCollection Date: 2021-01-01 DOI:10.1177/20363613211034710
Karlton Wong, Jomjit Chantharasamee, Scott Nelson, Mark A Eckardt, Kambiz Motamedi, Francis J Hornicek, Arun S Singh
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引用次数: 5

摘要

成骨细胞瘤和动脉瘤性骨囊肿(ABC)是罕见的良性骨肿瘤,约占原发性骨恶性肿瘤的1%-2%,通常发生在中位年龄为20岁的年轻患者中,最常见于中轴骨骼。abc可以独立发展为原发性病变,也可以继发于其他骨病变,包括成骨细胞瘤、成软骨细胞瘤和巨细胞瘤。不可切除或广泛的成骨细胞瘤的治疗是具有挑战性的。2013年,美国食品和药物管理局(FDA)批准了denosumab用于治疗骨巨细胞瘤,因为它对这些病态的骨病变有疗效。各种病例报告显示成骨细胞瘤对地诺单抗有反应。此外,许多ABC病例报告描述了denosumab在这些情况下的疗效。我们在此描述一个独特的情况下,一个年轻的患者与侵袭性成骨细胞瘤和继发性abc谁是成功地用地诺单抗治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Aggressive osteoblastoma with a secondary aneurysmal bone cyst treated with denosumab.

Osteoblastomas and aneurysmal bone cysts (ABC) are rare benign bone tumors that make up about 1%-2% of primary bone malignancies, typically occurring in young patients with a median age of 20 years, most commonly effecting the axial skeleton. ABCs may develop independently as primary lesions, or secondary to other bony lesions including osteoblastomas, chondroblastomas, and giant cell tumors. Treatment of unresectable or extensive osteoblastomas can be challenging. In 2013, the Food and Drug Administration (FDA) approved denosumab for the treatment of giant cell tumors of the bone due to its efficacy in these morbid bony lesions. Various case reports have shown that osteoblastomas can respond to denosumab. Furthermore, numerous ABC case reports have described the efficacy of denosumab in these situations. We herein describe a unique case of a young patient with an aggressive osteoblastoma and secondary ABCs who was successfully treated with denosumab.

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来源期刊
Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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