对布洛芬过敏的转甲状腺素淀粉样变性患者成功的双氟尼拉脱敏1例报告

J. Aw, Siau Hui Low, Chuan Poh Lim, Kwok Wai Adrian Chan
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引用次数: 1

摘要

背景:淀粉样蛋白疾病是遗传性的,包括转甲状腺素(TTR)淀粉样变性,其中TTR基因的亚基蛋白突变可能发生,导致细胞外组织中原纤维(低分子量亚基(5至25 KD的蛋白质)的沉积。通过减少TTR淀粉样蛋白的形成,非甾体抗炎药双氟尼拉可以保持生活质量并显著减少疾病进展。我们报告一例61岁男性患者,有布洛芬过敏史,诊断为TTR淀粉样变性,并发周围神经病变,心脏和肝脏淀粉样变性。布洛芬口服激发试验后出现双侧轻度眼部肿胀。由于羧酸具有类似的结构主链,他可能对二氟尼柳产生假性过敏,发生过敏反应的可能性未知。目的:本研究旨在为TTR淀粉样变患者设计成功的双氟尼松脱敏治疗。方法:采用双氟尼拉500 mg 2片,溶解于8.4%碳酸氢钠注射液40 mL中,连续稀释10倍,进行14步双氟尼拉脱敏。口服脱敏以每隔30分钟剂量递增的方式进行,起始剂量为0.1 mg,直至达到最终剂量为250 mg。结果:患者耐受双氟尼拉脱敏,并继续双氟尼拉治疗,无任何过敏反应的证据。结论:对有布洛芬过敏史的患者,在没有其他治疗方法的情况下,可考虑使用双氟尼拉脱敏。据我们所知,这是第一篇描述布洛芬血管性水肿患者脱敏后能耐受口服双氟尼松的文章。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful Diflunisal Desensitization in a Transthyretin Amyloidosis Patient With Ibuprofen Allergy: A Case Report
Background: Amyloid diseases are hereditary and include transthyretin (TTR) amyloidosis where subunit protein mutations may occur in genes for TTR, leading to the deposition of fibrils (low molecular weight subunits (5 to 25 KD of proteins) in extracellular tissues. By reducing the formation of TTR amyloid, diflunisal, a nonsteroidal anti-inflammatory drug, can preserve the quality of life and significantly reduce disease progression. We present a case of a 61-year-old male patient with a history of ibuprofen allergy, diagnosed with TTR amyloidosis, complicated with peripheral neuropathy, cardiac, and liver amyloid. He developed bilateral mild eye swelling from the ibuprofen oral provocation test. With a similar structural backbone of carboxylic acid, he could develop pseudoallergy to diflunisal with an unknown likelihood of developing an allergic reaction. Objectives: This study aims to design successful diflunisal desensitization in a patient with TTR amyloidosis. Methods: The patient underwent a 14-step diflunisal desensitization procedure using 2 tablets of diflunisal 500 mg that was dissolved in 40 mL of sodium bicarbonate 8.4% injection to create serial 10-fold dilutions. Oral desensitization was administered in the escalation of the doses at 30-min intervals, with a starting dose of 0.1 mg until a final dose of 250 mg was reached. Results: The patient tolerated diflunisal desensitization and was continued on diflunisal treatment without any evidence of an allergic reaction. Conclusion: Diflunisal desensitization can be considered in patients with a history of ibuprofen allergy if there are no available alternative treatments. To the best of our knowledge, this is the first article describing a patient with angioedema to ibuprofen who could tolerate oral diflunisal after desensitization.
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