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卡比马唑引起的粒细胞缺乏症。

Carbimazole-induced agranulocytosis.

作者信息

Mohan Anisha, Joseph Siby, Sidharthan Neeraj, Murali Dhanya

机构信息

Department of Pharmacy Practice, Amrita School of Pharmacy, Kochi, Kerala, India.

Department of Oncology, Amrita Institute of Medical Sciences, Amrita Viswa Vidyapeetam University, AIMS - Kochi Campus, Kochi, Kerala, India.

出版信息

J Pharmacol Pharmacother. 2015 Oct-Dec;6(4):228-30. doi: 10.4103/0976-500X.171881.

Abstract

UNLABELLED

A 47 year old lady with hyperthyroidism for past 1½ years was initially on Carbimazole 20 mg orally then changed to 30 mg (during Hysterectomy) but was taking 10 mg for last 1 year. She had intermittent fever with severe B/L bifrontal headache since 3 weeks. Routine investigations showed anaemia, neutropenia, leucopenia and CRP elevation. Peripheral smear showed normocytic normochromic anaemia with Rouleaux formation, leucopenia with 2% atypical cells and mild thrombocytosis. Widal test, RA factor (Rheumatoid factor) test, Ig M (Immunoglobulin M) dengue, Ig M Lepto, TORCH infections (Toxoplasmosis, Other (Syphilis, varicella-zoster, parvovirus B19), Cytomegalovirus and Herpes infections), ANA (Antinuclear antibody) screen cANCA (Cytoplasmic antineutrophil cytoplasmic antibodies) and pANCA (Perinuclear Anti-Neutrophil Cytoplasmic Antibodies) tests were negative. Bone marrow aspiration showed normo to hypercellular marrow with 15% atypical cells and plasma cells. Multiple myeloma workup was done. Carbimazole was withheld.

CONCLUSION

Drug induced agranulocytosis occurs with in 1-2 months of taking the antithyroid medication but onset delayed by 1½ year. De-challenge resulted normalization of blood parameters.

摘要

未标注

一名47岁女性,患有甲状腺功能亢进症已1年半,最初口服卡比马唑20毫克,后(在子宫切除术中)改为30毫克,但在过去1年一直服用10毫克。她自3周前开始出现间歇性发热,并伴有严重的双侧额部头痛。常规检查显示贫血、中性粒细胞减少、白细胞减少以及C反应蛋白升高。外周血涂片显示正细胞正色素性贫血伴红细胞缗钱状形成、白细胞减少伴2%非典型细胞以及轻度血小板增多。肥达试验、类风湿因子试验、IgM(免疫球蛋白M)登革热、IgM钩端螺旋体、TORCH感染(弓形虫病、其他(梅毒、水痘 - 带状疱疹、细小病毒B19)、巨细胞病毒和疱疹感染)、抗核抗体(ANA)筛查、胞浆抗中性粒细胞胞浆抗体(cANCA)和核周抗中性粒细胞胞浆抗体(pANCA)检测均为阴性。骨髓穿刺显示骨髓细胞数正常至高细胞数,有15%非典型细胞和浆细胞。进行了多发性骨髓瘤检查。停用了卡比马唑。

结论

药物性粒细胞缺乏症在服用抗甲状腺药物后的1 - 2个月内发生,但发病延迟了1年半。撤药后血液参数恢复正常。

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