Unusual occurrence of hemophagocytic lymphohistiocytosis in HIV-positive person with visceral leishmaniasis

IF 0.3 Q4 INFECTIOUS DISEASES HIV & AIDS Review Pub Date : 2021-01-01 DOI:10.5114/hivar.2021.111899
I. Kooli, W. Marrakchi, A. Toumi, A. Aouam, Hammouda Baba, M. Chakroun
{"title":"Unusual occurrence of hemophagocytic lymphohistiocytosis in HIV-positive person with visceral leishmaniasis","authors":"I. Kooli, W. Marrakchi, A. Toumi, A. Aouam, Hammouda Baba, M. Chakroun","doi":"10.5114/hivar.2021.111899","DOIUrl":null,"url":null,"abstract":"Introduction: Visceral leishmaniasis is a well-recognized opportunistic infection in people living with HIV (PLHIV). Unlike adults, in children this infection is frequently associated with hemophagocytic lymphohistiocytosis (HLH). We report a case of HLH in HIV-positive person with visceral leishmaniasis. Case description: A 25-year-old man known living with HIV since 2013 was admitted to infectious diseases department in March 2017. His clinical examination was clear. His initial viral load was 630,000 copies/mm 3 and CD4+ cells count was 12/mm 3 . No opportunistic infections were noted. The patient was started on antiretroviral therapy. During hospitalization, he developed fever, asthe-nia, rhinorrhea, and odynophagia. The diagnosis of HLH was retained because of pancytopenia, cytolysis, hyponatremia, high level of ferrinemia, and hemophagocytosis. Etiological investigations revealed positive Leishmania PCR. Also, Leishmania was detected in sternal puncture. Patient received meglumine antimoniate (glucantime) 20 mg/kg/day for 21 days with favorable outcomes. To prevent relapse, he received meglumine antimoniate 20 mg/kg/month as long as his CD4+ count was less than 100 cells/mm 3 . After 1-year follow up, no relapse was detected. Conclusions: Clinical and laboratory presentation of visceral leishmaniasis in PLHIV may differ from classic kala-azar. In our case, HLH was the reason for VL discovery.","PeriodicalId":53943,"journal":{"name":"HIV & AIDS Review","volume":null,"pages":null},"PeriodicalIF":0.3000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"HIV & AIDS Review","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5114/hivar.2021.111899","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Visceral leishmaniasis is a well-recognized opportunistic infection in people living with HIV (PLHIV). Unlike adults, in children this infection is frequently associated with hemophagocytic lymphohistiocytosis (HLH). We report a case of HLH in HIV-positive person with visceral leishmaniasis. Case description: A 25-year-old man known living with HIV since 2013 was admitted to infectious diseases department in March 2017. His clinical examination was clear. His initial viral load was 630,000 copies/mm 3 and CD4+ cells count was 12/mm 3 . No opportunistic infections were noted. The patient was started on antiretroviral therapy. During hospitalization, he developed fever, asthe-nia, rhinorrhea, and odynophagia. The diagnosis of HLH was retained because of pancytopenia, cytolysis, hyponatremia, high level of ferrinemia, and hemophagocytosis. Etiological investigations revealed positive Leishmania PCR. Also, Leishmania was detected in sternal puncture. Patient received meglumine antimoniate (glucantime) 20 mg/kg/day for 21 days with favorable outcomes. To prevent relapse, he received meglumine antimoniate 20 mg/kg/month as long as his CD4+ count was less than 100 cells/mm 3 . After 1-year follow up, no relapse was detected. Conclusions: Clinical and laboratory presentation of visceral leishmaniasis in PLHIV may differ from classic kala-azar. In our case, HLH was the reason for VL discovery.
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
hiv阳性内脏利什曼病患者嗜血球淋巴组织细胞增多症的罕见发生
内脏利什曼病是HIV感染者(PLHIV)中公认的机会性感染。与成人不同,在儿童中,这种感染通常与噬血细胞性淋巴组织细胞增多症(HLH)有关。我们报告一例HLH在hiv阳性的人内脏利什曼病。病例描述:一名自2013年以来已知感染艾滋病毒的25岁男子于2017年3月住进传染病科。他的临床检查很清楚。患者初始病毒载量为63万拷贝/mm 3, CD4+细胞计数为12个/mm 3。未发现机会性感染。病人开始接受抗逆转录病毒治疗。在住院期间,他出现发烧、咳嗽、流鼻水和咽痰。由于全血细胞减少、细胞溶解、低钠血症、高铁血症和噬血细胞症,HLH的诊断得以保留。病原学调查显示利什曼原虫PCR阳性。胸骨穿刺检出利什曼原虫。患者接受20 mg/kg/天的锑酸甲氨胺(葡聚糖)治疗21天,结果良好。为了防止复发,只要CD4+计数小于100个细胞/mm 3,就给予甲氨铵20 mg/kg/月。随访1年,无复发。结论:PLHIV患者内脏利什曼病的临床和实验室表现可能不同于经典黑热病。在我们的例子中,HLH是发现VL的原因。
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
HIV & AIDS Review
HIV & AIDS Review INFECTIOUS DISEASES-
CiteScore
0.50
自引率
0.00%
发文量
30
审稿时长
12 weeks
期刊最新文献
Developing Aysoo: a mobile-based self-management application for people living with HIV Survival analysis and predictors of mortality for adult HIV/AIDS patients following antiretroviral therapy in Mizan-Tepi University Teaching Hospital, Southwest Ethiopia: a retrospective cohort study Self-esteem and self-efficacy among HIV-positive adolescents: an intervention study Reverse transcriptase inhibition: a way to defeat HIV Primary syphilis as oral lesion in HIV/AIDS-positive patient: case report of unusual manifestation
×
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