Amelioration of Paget Disease of Bone After Denosumab for Osteopenia

Vijayvardhan Kamalumpundi BS , Elham Shams MD , Maisoon Torfah MD , Marcelo L. Correia MD, MSc, PhD
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引用次数: 1

Abstract

Background/Objective

Denosumab is a monoclonal antibody that inhibits bone resorption and is indicated for the treatment of osteoporosis, bone metastases, and giant cell tumor of bone. We describe a woman with symptomatic Paget disease of the skull whose headaches and monostotic disease of the skull improved after receiving denosumab for concomitant low bone density.

Case Report

A 75-year-old woman presented with unremitting headache of 1 month. She had a medical history of polymyalgia rheumatica, osteopenia, hypothyroidism, and gastroesophageal reflux disease. She reported taking prednisone 1 to 20 mg daily for polymyalgia rheumatica for 1 year and received a dose of denosumab 60 mg for osteopenia 1 month before presentation. The calcium, alkaline phosphatase, and bone-specific alkaline phosphatase levels were 8.2 mg/dL (reference range [RR], 8.5-10.5 mg/dL), 132 U/L (RR, 40-129 U/L), and 17.8 μg/L (RR, 7-22.4 μg/L), respectively. Skull radiography revealed sclerosis/hyperostosis, lytic lesions, and expansion of bone, consistent with Paget disease of bone (PDB). Five months after the initial presentation, her headache resolved, and her calcium and alkaline phosphatase levels were 9.7 U/L and 96 U/L, respectively.

Discussion

Denosumab neutralizes the receptor activator of nuclear factor-kappa B ligand. To date, there have been 2 case reports reported in the English literature of denosumab used successfully in patients with PDB who could not tolerate or were not eligible for bisphosphonates. This case report describes a patient with PDB treated with denosumab for osteopenia who experienced improvement in PDB-related symptoms.

Conclusion

Although denosumab was originally approved for the treatment of osteoporosis, the inhibition of bone resorption via inhibition of the receptor activator of nuclear factor-kappa B ligand may be potentially effective in the treatment of PDB.

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Denosumab治疗骨质疏松症后骨Paget病的改善。
背景/目的:Denosumab是一种抑制骨吸收的单克隆抗体,适用于治疗骨质疏松、骨转移和骨巨细胞瘤。我们描述了一名患有症状性颅骨Paget病的女性,其头痛和颅骨单发性疾病在接受替诺沙单抗治疗伴发的低骨密度后有所改善。病例报告:一位75岁的女性,持续头痛1个月。她有风湿病、骨质减少、甲状腺功能减退和胃食管反流病病史。据报道,她每天服用泼尼松1至20 mg治疗风湿性多肌痛,持续1年,并在出现症状前1个月服用剂量为60 mg的替诺沙单抗治疗骨质减少症。钙、碱性磷酸酶和骨特异性碱性磷酸酶水平分别为8.2 mg/dL(参考范围[RR],8.5-10.5 mg/dL)、132 U/L(RR,40-129 U/L)和17.8μg/L(RR,7-22.4μg/L)。颅骨X线片显示骨硬化/骨质增生、溶解性病变和骨膨胀,与骨Paget病(PDB)一致。初次就诊五个月后,她的头痛症状缓解,钙和碱性磷酸酶水平分别为9.7U/L和96U/L。讨论:Denosumab中和核因子κB配体的受体激活剂。到目前为止,英国文献中已经报道了2例狄诺沙单抗成功用于不能耐受或不符合双磷酸盐条件的PDB患者的病例报告。本病例报告描述了一名PDB患者,该患者在PDB相关症状方面有所改善。结论:尽管狄诺沙单抗最初被批准用于治疗骨质疏松症,但通过抑制核因子κB配体的受体激活剂来抑制骨吸收可能对PDB的治疗具有潜在的有效性。
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来源期刊
AACE Clinical Case Reports
AACE Clinical Case Reports Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.30
自引率
0.00%
发文量
61
审稿时长
55 days
期刊最新文献
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