Department of Medical Education, National Taiwan University Hospital, No.7, Zhongshan S. Rd Zhongzheng Dist., Taipei City 100, Taiwan, ROC.
Department of Dermatology, National Taiwan University Hospital and National Taiwan University College of Medicine, No.7, Zhongshan S. Rd Zhongzheng Dist., Taipei City 100, Taiwan, ROC.
Clin Drug Investig. 2020 Oct;40(10):915-926. doi: 10.1007/s40261-020-00956-w.
Idiosyncratic drug-induced neutropenia (DIN) is a rare, potentially fatal adverse reaction. A literature search was performed on Pubmed and Embase, targeting articles indicating neutropenia as a complication during the treatment of non-neoplastic dermatological disorders. In 66 identified articles, the common incriminated drugs included conventional oral immunomodulators, topical cytotoxic agents, antibacterials, antifungals, biologics and targeted synthetic disease-modifying antirheumatic drugs, non-steroidal anti-inflammatory drugs, and retinoids, with dapsone being reported most often. The duration of drug exposure before the diagnosis of neutropenia varied, but mostly ranged from days to weeks. The majority of patients recovered after drug discontinuation and supportive management including antibiotics and granulocyte colony-stimulating factor, but fatal cases were reported. The proposed pathogenesis of DIN consists of direct drug toxicity and immune-mediated reaction. Certain genetic variants, individual variability in enzyme efficiency, and concomitant use of other drugs may increase the risk of DIN. Being familiar with the most commonly implicated agents and risk factors helps early identification and prompt management of this potentially fatal complication.
药物诱导的中性粒细胞减少症(DIN)是一种罕见的、潜在致命的不良反应。在 PubMed 和 Embase 上进行了文献检索,目标是表明中性粒细胞减少症是治疗非肿瘤性皮肤病的并发症的文章。在 66 篇确定的文章中,常见的可疑药物包括传统口服免疫调节剂、局部细胞毒性药物、抗菌药物、抗真菌药物、生物制剂和靶向合成疾病修饰抗风湿药物、非甾体抗炎药和类视黄醇,其中报道最常见的是氨苯砜。诊断中性粒细胞减少症之前的药物暴露时间长短不一,但大多为数天至数周。大多数患者在停药和支持治疗(包括抗生素和粒细胞集落刺激因子)后恢复,但也有致命病例报告。DIN 的发病机制包括直接药物毒性和免疫介导反应。某些遗传变异、酶效率的个体差异以及同时使用其他药物可能会增加 DIN 的风险。熟悉最常涉及的药物和危险因素有助于早期识别和及时处理这种潜在致命的并发症。