Disseminated Histoplasmosis in Immunocompetent Patients Presented with Fever of Unknown Origin (FUO)

Md Sohidul Islam, M. R. Habib, Elmay Taswafe Asha, Mahbuba Sharmin, Mehnaj Ashraf, A. Mahmud, A. L. Kabir, M. R. Alam, F. Chowdhury
{"title":"Disseminated Histoplasmosis in Immunocompetent Patients Presented with Fever of Unknown Origin (FUO)","authors":"Md Sohidul Islam, M. R. Habib, Elmay Taswafe Asha, Mahbuba Sharmin, Mehnaj Ashraf, A. Mahmud, A. L. Kabir, M. R. Alam, F. Chowdhury","doi":"10.3329/jom.v24i1.64906","DOIUrl":null,"url":null,"abstract":"Histoplasmosis is underreported although in Southeast Asia including Bangladesh is thought to be endemic considering the favorable geo-climatic conditions for the organism. Non-recognition of histoplasmosis is particularly attributed to possible misdiagnosis as tuberculosis (which is endemic here and common in Bangladesh) because histoplasmosis mimics tuberculosis in clinical presentation, imaging and histopathology. Disseminated histoplasmosis mainly occur in immunocompromised patients and rare in immunocompetent subjects. Here we are reporting two cases of disseminated histoplasmosis where both were immunocompetent and presented with FUO. Both patients visited several health centers before coming to us with no definite diagnosis and we got them in a progressive stage. Both were confirmed through bone marrow study. Unfortunately, one of them died from disease progression, sepsis and other complications and another patient gradually improved with treatment (amphotericin B and itraconazole). We are reporting these cases to highlight the fact that disseminated histoplasmosis does occur in immunocompetent patient and may occur with or without pulmonary symptoms. A high index of suspicion is required for diagnosis and delay can often be fatal.\nJ MEDICINE 2023; 24: 59-64","PeriodicalId":76013,"journal":{"name":"Journal of medicine","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3329/jom.v24i1.64906","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

Histoplasmosis is underreported although in Southeast Asia including Bangladesh is thought to be endemic considering the favorable geo-climatic conditions for the organism. Non-recognition of histoplasmosis is particularly attributed to possible misdiagnosis as tuberculosis (which is endemic here and common in Bangladesh) because histoplasmosis mimics tuberculosis in clinical presentation, imaging and histopathology. Disseminated histoplasmosis mainly occur in immunocompromised patients and rare in immunocompetent subjects. Here we are reporting two cases of disseminated histoplasmosis where both were immunocompetent and presented with FUO. Both patients visited several health centers before coming to us with no definite diagnosis and we got them in a progressive stage. Both were confirmed through bone marrow study. Unfortunately, one of them died from disease progression, sepsis and other complications and another patient gradually improved with treatment (amphotericin B and itraconazole). We are reporting these cases to highlight the fact that disseminated histoplasmosis does occur in immunocompetent patient and may occur with or without pulmonary symptoms. A high index of suspicion is required for diagnosis and delay can often be fatal. J MEDICINE 2023; 24: 59-64
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
伴有不明原因发热(FUO)的免疫功能正常患者的弥散性组织胞浆菌病
考虑到适宜的地理气候条件,组织胞浆菌病在包括孟加拉国在内的东南亚被认为是地方性的,但报告不足。由于组织胞浆菌病在临床表现、影像学和组织病理学上与结核病相似,因此无法识别组织胞浆菌病特别归因于可能被误诊为结核病(这在这里是地方病,在孟加拉国很常见)。播散性组织胞浆菌病主要发生在免疫功能低下的患者中,在免疫功能正常的人群中很少见。在这里,我们报告两例播散性组织胞浆菌病,两者均具有免疫能力并表现为FUO。这两个病人在来我们这里之前都去过几家健康中心,没有明确的诊断,我们认为他们处于进展阶段。两例均经骨髓检查证实。不幸的是,其中一人死于疾病进展、败血症和其他并发症,另一名患者通过治疗(两性霉素B和伊曲康唑)逐渐好转。我们报告这些病例是为了强调这样一个事实,即播散性组织胞浆菌病确实发生在免疫功能正常的患者中,可能伴有或不伴有肺部症状。诊断需要高度的怀疑指数,延误往往是致命的。[J]中华医学杂志2023;24: 59 - 64
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
Obituary Vol. 25(2) Professor (Dr.) Md. Ridwanur Rahman Acquired Hemophilia A (AHA): A Rare Bleeding Disorder In a Tertiary Care Hospital In Dhaka, Bangladesh Clinical spectrum and risk factors of severe dengue among hospitalized patients - a cross-sectional study during the 2023 dengue epidemic in Bangladesh Acute Medicine – Needs and Challenges: The Bangladesh Perspective Exploring challenges, innovations, and technological integration in medical education after COVID-19 pandemic: An In-depth analysis
×
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