病例报告:单次低剂量地诺单抗触发双膦酸盐治疗后骨质疏松症患者MRONJ的发展。

IF 3 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Frontiers in oral health Pub Date : 2024-12-04 eCollection Date: 2024-01-01 DOI:10.3389/froh.2024.1473049
Dávid Száraz, Vojtěch Peřina, Jana Treglerová, Ctirad Macháček, Ondřej Zendulka, Petra Bořilová Linhartová
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引用次数: 0

摘要

denosumab (DMB)和双膦酸盐(bp)都是用于治疗骨质疏松症和肿瘤疾病的抗吸收药物(ARDs),众所周知,它们有可能导致药物相关性颌骨骨坏死(MRONJ)。除了ARDs,他汀类药物最近也与MRONJ的发展有关,特别是在服用高剂量他汀类药物较长时间的患者中。在这里,我们报告了一例使用他汀类药物并使用阿仑膦酸钠治疗3年的骨质疏松症女性患者,仅在单次低剂量DMB后迅速发展为MRONJ III期。上颌部分切除后完全愈合,无复发。我们对单次低剂量DMB引发MRONJ的病例进行了文献回顾,这些病例有或没有先前应用过其他ARDs。到目前为止,只有6例类似的患者在先前的BP治疗后单次低剂量DMB后发生MRONJ。除此之外,文献报道1例患者在接受romosozumab治疗后接受单剂量DMB后出现MRONJ, 5例患者在未接受ARD治疗的情况下接受单剂量DMB后出现MRONJ。我们建议在DMB治疗开始之前,应考虑所有诱发MRONJ发展的因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Case Report: single low-dose of denosumab as a trigger of MRONJ development in a patient with osteoporosis after bisphosphonate therapy.

Both denosumab (DMB) and bisphosphonates (BPs), antiresorptive drugs (ARDs) used for the treatment of osteoporosis and oncological disorders, are known for their potential to cause medication-related osteonecrosis of the jaws (MRONJ). Besides ARDs, statins were recently associated with MRONJ development, especially in patients taking higher doses of statins for a longer period of time. Here, we report a case of a female patient with osteoporosis using statins and treated with alendronate for 3 years who rapidly developed MRONJ stage III after only a single low dose of DMB. After partial maxillectomy complete healing was observed without any recurrence. We performed a literature review of cases with MRONJ triggered by a single low dose of DMB, with or without previous application of other ARDs. Only six similar cases of patients who developed MRONJ after a single low dose of DMB following previous BP therapy have been reported so far. Besides these, literature reports one patient who developed MRONJ after a single dose of DMB following romosozumab treatment and five cases developing MRONJ after a single dose of DMB even without any previous ARD treatment. We suggest that before DMB therapy is initiated, all factors predisposing to MRONJ development should be considered.

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来源期刊
CiteScore
3.30
自引率
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审稿时长
13 weeks
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