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迟发性氯氮平诱导的合并多发性硬化症患者的粒细胞缺乏症。

Late-onset clozapine-induced agranulocytosis in a patient with comorbid multiple sclerosis.

机构信息

Department of Psychiatry, National Institute of Mental Health And Neurosciences (NIMHANS), Bangalore-560029, India.

出版信息

Gen Hosp Psychiatry. 2013 Sep-Oct;35(5):574.e5-6. doi: 10.1016/j.genhosppsych.2012.07.001. Epub 2012 Aug 15.

Abstract

The risk of clozapine-induced agranulocytosis is highest in the initial 6 months after onset of treatment. There have been very few reports of neutropenia and agranulocytosis after this period. We report a unique case of delayed clozapine-induced agranulocytosis in a patient with preexisting multiple sclerosis (MS) which was treated with granulocyte colony-stimulating factor. Both MS and clozapine-induced agranulocytosis have an underlying autoimmune immune mechanism. This case highlights the need for frequent blood count monitoring on clozapine even after the initial 6 months of starting treatment especially in patients with a past history of drop in white blood cell counts as well as with a comorbid autoimmune disorder.

摘要

氯氮平引起的粒细胞缺乏症的风险在治疗开始后的最初 6 个月内最高。在此期间,中性粒细胞减少症和粒细胞缺乏症的报告非常少。我们报告了一例独特的、在预先存在的多发性硬化症(MS)患者中发生的、延迟出现的氯氮平诱导的粒细胞缺乏症,该患者使用了粒细胞集落刺激因子进行治疗。MS 和氯氮平诱导的粒细胞缺乏症都有潜在的自身免疫机制。该病例强调了即使在开始治疗后的最初 6 个月后,也需要频繁监测氯氮平的血象,特别是对于过去有白细胞计数下降病史以及合并自身免疫性疾病的患者。

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