Azathioprine-induced Myelodysplasia Mimicking Myelodysplastic Syndrome

M. Ohe
{"title":"Azathioprine-induced Myelodysplasia Mimicking Myelodysplastic Syndrome","authors":"M. Ohe","doi":"10.12771/EMJ.2019.42.3.46","DOIUrl":null,"url":null,"abstract":"An 81-year-old man suffering from autoimmune hepatitis, who had been on prednisolone (10–20 mg/day) and azathioprine (AZA) (50 mg/day) for about 5 months, was diagnosed with macrocytic anemia during a routine examination. Before treatment with prednisolone and AZA, complete blood count revealed a white blood cell count of 9,780/μL, hemoglobin level of 11.7 g/dL with a mean corpuscular volume of 91.9 fL (normal range, 80–99 fL), and platelet count of 18.4×10/μL. Five months after treatment with prednisolone and AZA, complete blood count revealed a white blood cell count of 6,180/μL, hemoglobin level of 7.2 g/dL with a mean corpuscular volume of 109.1 fL, and platelet count of 17.5×10/μL. Serological tests revealed iron level of 116 μg/dL (normal range, 40–190 μg/ dL), free thyroxine level of 1.10 ng/dL (normal range, 0.9–1.70 ng/dL), vitamin B12 level of 462 pg/mL (normal range, 233–914 pg/mL), folic acid level of 7.4 ng/mL (normal range, 3.6–12.9 ng/mL), and anti-DNA antibody (Ab) level of <1.7 IU/mL (normal value, <6.0 IU/mL). The results of tests for antivirus immunoglobulin M (IgM) Ab were negative for antiparvovirus B19 IgM Ab, anti-Epstein-Barr virus capsid antigen IgM Ab, and anti-cytomegalovirus IgM Ab. Bone marrow aspiration revealed a normocellular bone marrow. The aspiration smear revealed a neutrophil with hypersegmentation (Fig. 1), an erythroblast with a bilobulated nucleus (Fig. 2A), an erythroblast with abundant cytoplasm and a multilobulated nucleus (Fig. 2B), an erythroblast with a multilobulated nucleus and HowellJolly bodies (Fig. 2C), an erythrocyte with abundant cytoplasm and Howell-Jolly bodies (Fig. 2D), and a megakaryocyte with separated nuclei (Fig. 3). However, no chromosomal aberrations were observed. Based on these findings, vitamin B12 or folic acid deficiency, viral infections, and systemic lupus erythematosus that led to anemia with myelodysplasia were not diagnosed. Considering AZA-induced hematopoietic disorder, AZA treatment was discontinued, leading to normalization of macrocytic Images and Solution Ewha Med J 2019;42(3):46-47 https://doi.org/10.12771/emj.2019.42.3.46 eISSN 2234-2591","PeriodicalId":197820,"journal":{"name":"The Ewha Medical Journal","volume":"116 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Ewha Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12771/EMJ.2019.42.3.46","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

An 81-year-old man suffering from autoimmune hepatitis, who had been on prednisolone (10–20 mg/day) and azathioprine (AZA) (50 mg/day) for about 5 months, was diagnosed with macrocytic anemia during a routine examination. Before treatment with prednisolone and AZA, complete blood count revealed a white blood cell count of 9,780/μL, hemoglobin level of 11.7 g/dL with a mean corpuscular volume of 91.9 fL (normal range, 80–99 fL), and platelet count of 18.4×10/μL. Five months after treatment with prednisolone and AZA, complete blood count revealed a white blood cell count of 6,180/μL, hemoglobin level of 7.2 g/dL with a mean corpuscular volume of 109.1 fL, and platelet count of 17.5×10/μL. Serological tests revealed iron level of 116 μg/dL (normal range, 40–190 μg/ dL), free thyroxine level of 1.10 ng/dL (normal range, 0.9–1.70 ng/dL), vitamin B12 level of 462 pg/mL (normal range, 233–914 pg/mL), folic acid level of 7.4 ng/mL (normal range, 3.6–12.9 ng/mL), and anti-DNA antibody (Ab) level of <1.7 IU/mL (normal value, <6.0 IU/mL). The results of tests for antivirus immunoglobulin M (IgM) Ab were negative for antiparvovirus B19 IgM Ab, anti-Epstein-Barr virus capsid antigen IgM Ab, and anti-cytomegalovirus IgM Ab. Bone marrow aspiration revealed a normocellular bone marrow. The aspiration smear revealed a neutrophil with hypersegmentation (Fig. 1), an erythroblast with a bilobulated nucleus (Fig. 2A), an erythroblast with abundant cytoplasm and a multilobulated nucleus (Fig. 2B), an erythroblast with a multilobulated nucleus and HowellJolly bodies (Fig. 2C), an erythrocyte with abundant cytoplasm and Howell-Jolly bodies (Fig. 2D), and a megakaryocyte with separated nuclei (Fig. 3). However, no chromosomal aberrations were observed. Based on these findings, vitamin B12 or folic acid deficiency, viral infections, and systemic lupus erythematosus that led to anemia with myelodysplasia were not diagnosed. Considering AZA-induced hematopoietic disorder, AZA treatment was discontinued, leading to normalization of macrocytic Images and Solution Ewha Med J 2019;42(3):46-47 https://doi.org/10.12771/emj.2019.42.3.46 eISSN 2234-2591
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
硫唑嘌呤诱导的骨髓发育异常模拟骨髓增生异常综合征
81岁男性,自身免疫性肝炎患者,经强的松龙(10 - 20mg /天)和硫唑嘌呤(50mg /天)治疗约5个月,在常规检查中诊断为大细胞性贫血。在泼尼松龙和AZA治疗前,全血细胞计数显示白细胞计数9780 /μL,血红蛋白水平11.7 g/dL,平均红细胞体积91.9 fL(正常范围80-99 fL),血小板计数18.4×10/μL。强的松龙联合AZA治疗5个月后,全血细胞计数显示白细胞计数6180 /μL,血红蛋白水平7.2 g/dL,平均红细胞体积109.1 fL,血小板计数17.5×10/μL。血清学检查显示铁水平116 μg/dL(正常范围40 ~ 190 μg/dL),游离甲状腺素水平1.10 ng/dL(正常范围0.9 ~ 1.70 ng/dL),维生素B12水平462 pg/mL(正常范围233 ~ 914 pg/mL),叶酸水平7.4 ng/mL(正常范围3.6 ~ 12.9 ng/mL),抗dna抗体(Ab)水平<1.7 IU/mL(正常值<6.0 IU/mL)。抗细小病毒B19 IgM抗体、抗eb病毒衣壳抗原IgM抗体、抗巨细胞病毒IgM抗体检测结果均为阴性。骨髓穿刺显示骨髓细胞正常。抽吸涂片显示嗜中性粒细胞有过分割(图1),红母细胞有双叶状核(图2A),红母细胞有丰富的细胞质和多分叶状核(图2B),红母细胞有多分叶状核和Howell-Jolly小体(图2C),红细胞有丰富的细胞质和Howell-Jolly小体(图2D),巨核细胞有分离的细胞核(图3)。然而,没有观察到染色体畸变。基于这些发现,没有诊断出维生素B12或叶酸缺乏、病毒感染和系统性红斑狼疮导致贫血并骨髓发育不良。考虑到AZA诱导的造血障碍,停止AZA治疗,导致大细胞图像和溶液正常化Ewha Med 2019;42(3):46-47 https://doi.org/10.12771/emj.2019.42.3.46 eISSN 2234-2591
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Gender equity in medical journals in Korea and this issue Sex differences in pharmacotherapy for heart failure Sex and Gender Equity in Research (SAGER): rationale for the SAGER guidelines and recommended use: a Korean translation Endoscopically resected duodenal lipoma as an uncommon cause of upper gastrointestinal bleeding: a case report Disseminated cutaneous gout: a rare manifestation of gout
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1