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地诺单抗治疗因反弹性高钙血症而受损的小儿胫骨动脉瘤样骨囊肿的疗效

The Efficacy of Denosumab in the Management of a Tibial Paediatric Aneurysmal Bone Cyst Compromised by Rebound Hypercalcaemia.

作者信息

Harcus Matthew, Aldridge Samantha, Abudu Adesegun, Jeys Lee, Senniappan Senthil, Morgan Henry, Pizer Barry

机构信息

Department of Paediatric Oncology, Alder Hey NHS Foundation Trust, Liverpool, UK.

Department of Paediatric Nephrology, Alder Hey NHS Foundation Trust, Liverpool, UK.

出版信息

Case Rep Pediatr. 2020 Dec 9;2020:8854441. doi: 10.1155/2020/8854441. eCollection 2020.

Abstract

Surgery is the main treatment option for patients with aneurysmal bone cyst (ABC). We report our experience of using denosumab as an alternative treatment in a child with a multiply recurrent and unresectable tibial ABC. The efficacy and safety of denosumab in the paediatric population, and in the treatment of ABC, are still to be fully evaluated. We describe a 13-year-old boy with an extensive and aggressive ABC involving the proximal tibia, which had recurred following multiple previous surgeries. The patient had ongoing severe pain, was unable to weight-bear, and was at significant risk of pathological fracture. En bloc resection and embolization were not deemed viable, and a decision to use denosumab was made. He received 17 doses of subcutaneous denosumab (70 mg/m) over a 27-month period, at increasing dose intervals. His symptoms significantly improved, and bony consolidation was observed within six months of treatment. He was able to walk without protection and fully weight-bear without any pain by 18 months. With an increase to a six-month dosing interval, the patient presented with a severe, symptomatic rebound hypercalcaemia requiring bisphosphonate therapy. This reoccurred on two further occasions. This case adds to the evidence that denosumab is effective in the treatment of ABC in paediatric patients, but there is a risk of rebound hypercalcaemia. Therefore, patient awareness and biochemical monitoring for rebound hypercalcaemia are essential.

摘要

手术是骨动脉瘤样囊肿(ABC)患者的主要治疗选择。我们报告了在一名患有多次复发且无法切除的胫骨ABC的儿童中使用地诺单抗作为替代治疗的经验。地诺单抗在儿科人群以及ABC治疗中的疗效和安全性仍有待全面评估。我们描述了一名13岁男孩,患有累及胫骨近端的广泛侵袭性ABC,此前多次手术均复发。患者持续存在严重疼痛,无法负重,并有发生病理性骨折的重大风险。整块切除和栓塞被认为不可行,因此决定使用地诺单抗。在27个月的时间里,他接受了17剂皮下注射地诺单抗(70mg/m),给药间隔逐渐增加。他的症状明显改善,治疗6个月内观察到骨愈合。到18个月时,他能够无需保护行走,完全负重且无任何疼痛。随着给药间隔增加到6个月,患者出现严重的、有症状的反弹性高钙血症,需要双膦酸盐治疗。这种情况又再次出现了两次。该病例进一步证明地诺单抗对儿科ABC患者有效,但存在反弹性高钙血症的风险。因此,提高患者对反弹性高钙血症的认识并进行生化监测至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d220/7746474/e2bd5e28db0f/CRIPE2020-8854441.001.jpg

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