METHIMAZOLE-INDUCED AGRANULOCYTOSIS AND SEPSIS: WAS THYROID STORM PRESENT OR JUST BEING MIMICKED?

M A M Stumpf, G C A Schrut, M Ramthun, S Onuma, H E C G Osternack
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引用次数: 4

Abstract

Introduction: Agranulocytosis induced by thioamides is rare, occurring only in 0.2-0.5% of cases.

Case presentation: We present the case of a 45-year-old woman previously diagnosed with Graves' disease that discontinued the use of methimazole on her own. She attended the Emergency Department presenting fever (40.5¯C), agitation and diaphoresis. A thyroid storm diagnosis was initially thought, but after laboratory results showing neutrophil count near 0.06x109/L, sepsis due to neutropenia seemed the most logical hypothesis. Cephepime was promptly initiated. For thyrotoxicosis management, cholestyramine and atenolol were prescribed. In her second day of hospitalization, subcutaneous granulocyte colony-stimulating factor was started for an earlier medullar response. The patient was discharged after 7 days with atenolol 50mg/day and instructed to have a definite treatment for Graves disease as soon as possible.

Conclusion: Such case purpose is to remember clinicians that sepsis diagnosis can be challenged, especially when a thyroid storm is a possible diagnosis as well. In this particular case, both conditions should be treated, but life-threatening sepsis should have the focus for a quick therapeutic approach.

甲巯咪唑诱导的粒细胞缺乏症和败血症:甲状腺风暴是存在的还是只是模仿的?
简介:由硫胺引起的粒细胞缺乏症是罕见的,仅发生在0.2-0.5%的病例。病例介绍:我们提出的情况下,45岁的妇女以前诊断为格雷夫斯病,停止使用甲巯咪唑自己。她因发烧(40.5°C)、躁动和出汗而进入急诊科。最初认为是甲状腺风暴诊断,但实验室结果显示中性粒细胞计数接近0.06 × 109/L,中性粒细胞减少引起的败血症似乎是最合乎逻辑的假设。立即开始使用头孢吡肟。对于甲状腺毒症的治疗,开了胆胺和阿替洛尔。在她住院的第二天,开始皮下粒细胞集落刺激因子治疗早期髓质反应。患者给予阿替洛尔50mg/天治疗7天后出院,嘱尽快明确Graves病治疗。结论:本病例的目的是提醒临床医生,败血症的诊断可能会受到挑战,特别是当甲状腺风暴也是可能的诊断时。在这种特殊情况下,这两种情况都应该得到治疗,但危及生命的败血症应该集中在快速治疗方法上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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