Methimazole-Induced Pancytopenia with ANCA Positivity: Diagnostic and Management Challenges.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Sanhitha Valasareddy, Farina Tariq, Muhammad Zaheer
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引用次数: 0

Abstract

BACKGROUND Pancytopenia is an exceedingly rare adverse effect of antithyroid medications. It can be associated with both propylthiouracil and methimazole. While agranulocytosis is a more common adverse effect, pancytopenia has unique diagnostic and management issues due to its potential severity. CASE REPORT We present the case of a 36-year-old woman who presented to the Emergency Department with pancytopenia 2 months after starting methimazole for Grave's disease. Her case was complicated by severe candidemia and Serratia bacteremia. Laboratory workup revealed positive cytoplasmic and perinuclear anti-neutrophil cytoplasmic antibodies (ANCA) on immunofluorescence testing, with negative results on ELISA for MPO and PR3 antibodies. These findings were attributed to methimazole-induced ANCA positivity rather than primary ANCA-associated vasculitis. Methimazole was discontinued, and the patient was managed with aggressive antimicrobial therapy and supportive care, including blood transfusions and antifungal treatment. Despite the complexity of her condition, she survived after several months of intensive care and showed gradual improvement in blood counts and overall clinical status. CONCLUSIONS This case underscores the importance of recognizing potential iatrogenic causes of pancytopenia in patients receiving antithyroid medications. Early identification, prompt discontinuation of the offending agent, and comprehensive supportive care are essential for positive outcomes. This case also highlights the necessity for vigilant monitoring, patient education, and regular follow-up in individuals on antithyroid medications to prevent severe complications, morbidity, and mortality associated with rare but serious adverse effects like pancytopenia.

甲巯咪唑诱导的ANCA阳性全血细胞减少症:诊断和管理挑战。
背景:全血细胞减少症是抗甲状腺药物极为罕见的不良反应。它可以与丙基硫脲嘧啶和甲巯咪唑结合。虽然粒细胞缺乏症是一种更常见的不良反应,但全血细胞减少症由于其潜在的严重性而具有独特的诊断和管理问题。病例报告我们提出的情况下,36岁的妇女谁提出了急诊科全血细胞减少2个月后,开始甲巯咪唑治疗格雷夫斯病。患者并发严重念珠菌血症和沙雷菌血症。实验室检查显示免疫荧光检测细胞质和核周抗中性粒细胞细胞质抗体(ANCA)阳性,ELISA检测MPO和PR3抗体阴性。这些发现归因于甲巯咪唑诱导的ANCA阳性,而不是原发性ANCA相关血管炎。停用甲巯咪唑,患者接受积极的抗菌治疗和支持性护理,包括输血和抗真菌治疗。尽管她的病情复杂,但经过几个月的重症监护,她存活了下来,血液计数和整体临床状况逐渐改善。结论:本病例强调了在接受抗甲状腺药物治疗的患者中认识到全血细胞减少的潜在医源性原因的重要性。早期识别,及时停用致病药物,以及全面的支持性护理对取得积极结果至关重要。本病例也强调了警惕监测、患者教育和定期随访抗甲状腺药物的必要性,以预防与全血细胞减少症等罕见但严重的不良反应相关的严重并发症、发病率和死亡率。
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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来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
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