Yang Jing, Zhong Jing, Zhou Ling-Zhi, Hong Tao, Xiao Xin-Hua, Wen Ge-Bo
Department of Metabolism & Endocrinology of the First Affiliated Hospital, University of South China, China.
Intern Med. 2012;51(16):2189-92. doi: 10.2169/internalmedicine.51.7845. Epub 2012 Aug 15.
Agranulocytosis is a rare adverse effect of methimazole. The usual duration of treatment prior to the onset of agranulocytosis is approximately 1 to 4 months, and can be as long as 1 year. Agranulocytosis together with hepatotoxicity is an extremely rare idiosyncratic side effect of methimazole treatment. We present an unprecedented case of a Grave's disease patient who showed a strong reaction to methimazole with obvious agranulocytosis and hepatotoxicity which developed only six days after administration. This case, along with a literature review, is offered with the aim to increase the awareness of physicians of sudden onset agranulocytosis and hepatotoxicity from methimazole.
粒细胞缺乏症是甲巯咪唑一种罕见的不良反应。粒细胞缺乏症发作前的通常治疗持续时间约为1至4个月,最长可达1年。粒细胞缺乏症与肝毒性一起是甲巯咪唑治疗极其罕见的特异质性副作用。我们报告了一例前所未有的格雷夫斯病患者病例,该患者对甲巯咪唑反应强烈,出现明显的粒细胞缺乏症和肝毒性,且在用药仅六天后就发生了。本文结合文献综述呈现此病例,旨在提高医生对甲巯咪唑引发的突发粒细胞缺乏症和肝毒性的认识。