Valasareddy Sanhitha, Tariq Farina, Zaheer Muhammad
Division of Rheumatology, Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO, USA.
Department of Medicine, Quaid e Azam Medical College, Bahawalpur, Pakistan.
Am J Case Rep. 2025 May 5;26:e947323. doi: 10.12659/AJCR.947323.
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.
全血细胞减少是抗甲状腺药物极为罕见的不良反应。它可与丙硫氧嘧啶和甲巯咪唑相关。虽然粒细胞缺乏症是更常见的不良反应,但由于全血细胞减少的潜在严重性,其具有独特的诊断和管理问题。病例报告:我们报告一例36岁女性病例,该患者在开始服用甲巯咪唑治疗格雷夫斯病2个月后因全血细胞减少就诊于急诊科。她的病例因严重念珠菌血症和沙雷菌血症而复杂化。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胞浆抗体(ANCA)呈阳性,而MPO和PR3抗体的ELISA检测结果为阴性。这些发现归因于甲巯咪唑诱导的ANCA阳性,而非原发性ANCA相关性血管炎。停用甲巯咪唑,患者接受积极的抗菌治疗和支持治疗,包括输血和抗真菌治疗。尽管病情复杂,但经过数月的重症监护,她存活下来,血细胞计数和整体临床状况逐渐改善。结论:该病例强调了认识接受抗甲状腺药物治疗患者全血细胞减少潜在医源性原因的重要性。早期识别、迅速停用致病药物以及全面的支持治疗对于取得良好结果至关重要。该病例还凸显了对服用抗甲状腺药物的个体进行密切监测、患者教育和定期随访的必要性,以预防与全血细胞减少等罕见但严重不良反应相关的严重并发症、发病率和死亡率。