Azathioprine Hypersensitivity Syndrome during Treatment of Severe Interstitial Lung Disease with Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis.

Q4 Medicine Case Reports in Pulmonology Pub Date : 2020-07-03 eCollection Date: 2020-01-01 DOI:10.1155/2020/8852441
Eri Nakano, Tomohiko Asakawa, Mea Asou, Eri Nohara, Tomoyuki Seki, Makoto Araki
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引用次数: 1

Abstract

Azathioprine is used to treat anti-neutrophil cytoplasmic antibody- (ANCA-) associated vasculitis. Azathioprine hypersensitivity syndrome is often missed. An 81-year-old man undergoing treatment for interstitial pneumonia developed a high fever and was diagnosed with ANCA-associated vasculitis based on an elevated myeloperoxidase- (MPO-) ANCA titer and renal biopsy findings. After induction therapy, his clinical symptoms improved, but his MPO-ANCA remained elevated (>300 U·L-1) and hematuria persisted. Prednisolone plus azathioprine was administered as maintenance therapy. Three exacerbations of the inflammatory response occurred during the subsequent 3 months. In each instance, we suspected opportunistic infection or a flare-up of vasculitis. The first exacerbation was treated with an increased prednisolone dose and antibiotics. At the onset of the second exacerbation, which was accompanied by systemic erythema, we stopped azathioprine and administered antibiotics. The third exacerbation, which occurred the day after restarting azathioprine, involved a fever with chills and an acute inflammatory reaction; we therefore suspected an azathioprine allergy. A drug provocation test was performed, and a hyperinflammatory response was observed. The patient received prednisolone (15 mg·day-1) monotherapy; no further fever was observed during the subsequent 2 months. We therefore diagnosed azathioprine hypersensitivity syndrome. Under treatment with prednisolone (5 mg·day-1) and mycophenolate mofetil (1 g·day-1) (replacing the azathioprine), no signs of relapse or infection have occurred for more than two years. Renal function and the pulmonary lesions are stable, although the high MPO-ANCA titer and hematuria persist. The diagnosis of azathioprine hypersensitivity is often delayed because of the difficulty in identifying the relationship between immunosuppressive agents and hypersensitivity and in distinguishing this from infection or relapse of the primary disease. The misdiagnosis of azathioprine hypersensitivity leads to unnecessary treatment; thus, clinicians should consider allergic reactions specific to azathioprine when switching from induction to maintenance therapy.

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抗中性粒细胞细胞质抗体相关血管炎治疗重症间质性肺病期间硫唑嘌呤超敏综合征
硫唑嘌呤用于治疗抗中性粒细胞细胞质抗体- (ANCA-)相关血管炎。硫唑嘌呤超敏综合征常被忽略。一名接受间质性肺炎治疗的81岁男性出现高烧,根据髓过氧化物酶(MPO-) ANCA滴度升高和肾活检结果诊断为ANCA相关性血管炎。诱导治疗后,患者临床症状有所改善,但MPO-ANCA仍然升高(>300 U·L-1),血尿持续存在。泼尼松龙加硫唑嘌呤作为维持治疗。在随后的3个月内出现了3次炎症反应加重。在每个病例中,我们都怀疑是机会性感染或血管炎的突然发作。第一次加重时使用增加泼尼松龙剂量和抗生素治疗。在第二次发作时,伴有全身红斑,我们停用硫唑嘌呤并给予抗生素。第三次加重发生在重新使用硫唑嘌呤的第二天,包括发烧伴发冷和急性炎症反应;因此我们怀疑是硫唑嘌呤过敏。进行药物激发试验,观察到高炎症反应。患者接受强的松龙单药治疗(15 mg·day-1);随后2个月未见发热。因此,我们诊断为硫唑嘌呤过敏综合征。在强的松龙(5mg·day-1)和霉酚酸酯(1g·day-1)(替代硫唑嘌呤)治疗下,两年以上未发生复发或感染迹象。肾功能和肺部病变稳定,尽管高MPO-ANCA滴度和血尿持续存在。由于难以确定免疫抑制剂与过敏之间的关系以及难以将其与感染或原发疾病的复发区分开来,偶氮嘌呤超敏反应的诊断常常被推迟。硫唑嘌呤超敏症的误诊导致不必要的治疗;因此,当从诱导治疗转为维持治疗时,临床医生应考虑硫唑嘌呤的过敏反应。
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来源期刊
Case Reports in Pulmonology
Case Reports in Pulmonology Medicine-Pulmonary and Respiratory Medicine
CiteScore
1.80
自引率
0.00%
发文量
23
审稿时长
13 weeks
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