Identification of Irpex and Rhodotorula on surveillance bronchoscopy in a pediatric lung transplant recipient: A case report and review of literature of these atypical fungal organisms

IF 1.2 4区 医学 Q3 PEDIATRICS Pediatric Transplantation Pub Date : 2024-04-16 DOI:10.1111/petr.14759
Daniel T. Atwood, Julia R. Köhler, Sara O. Vargas, Wai Wong, Timothy Klouda
{"title":"Identification of Irpex and Rhodotorula on surveillance bronchoscopy in a pediatric lung transplant recipient: A case report and review of literature of these atypical fungal organisms","authors":"Daniel T. Atwood, Julia R. Köhler, Sara O. Vargas, Wai Wong, Timothy Klouda","doi":"10.1111/petr.14759","DOIUrl":null,"url":null,"abstract":"BackgroundInvasive fungal disease (IFD) is a frequent complication in pediatric lung transplant recipients, occurring in up to 12% of patients in the first year. Risk factors for infection include impaired lung defenses and intense immunosuppressive regimens. While most IFD occurs from <jats:italic>Aspergillus</jats:italic>, other fungal conidia are continuously inhaled, and infections with fungi on a spectrum of human pathogenicity can occur.Case ReportWe report a case of a 17‐year‐old lung transplant recipient in whom <jats:italic>Irpex lacteus</jats:italic> and <jats:italic>Rhodotorula</jats:italic> species were identified during surveillance bronchoscopy. She was asymptomatic and deemed to be colonized by <jats:italic>Irpex lacteus</jats:italic> and <jats:italic>Rhodotorula</jats:italic> species following transplant. 2 years after transplantation, she developed a fever, respiratory symptoms, abnormal lung imaging, and histological evidence of acute and chronic bronchitis on transbronchial biopsy. After developing symptoms concerning for a pulmonary infection and graft dysfunction, she was treated for a presumed IFD. Unfortunately, further diagnostic testing could not be performed at this time given her tenuous clinical status. Despite the initiation of antifungal therapy, her graft function continued to decline resulting in a second lung transplantation.ConclusionsThis case raises the concern for IFD in lung transplant recipients from <jats:italic>Irpex</jats:italic> species. Further investigation is needed to understand the pathogenicity of this organism, reduce the incidence and mortality of IFD in lung transplant recipients, and refine the approach to diagnosis and manage the colonization and isolation of rare, atypical fungal pathogens in immunocompromised hosts.","PeriodicalId":20038,"journal":{"name":"Pediatric Transplantation","volume":null,"pages":null},"PeriodicalIF":1.2000,"publicationDate":"2024-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric Transplantation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/petr.14759","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

Abstract

BackgroundInvasive fungal disease (IFD) is a frequent complication in pediatric lung transplant recipients, occurring in up to 12% of patients in the first year. Risk factors for infection include impaired lung defenses and intense immunosuppressive regimens. While most IFD occurs from Aspergillus, other fungal conidia are continuously inhaled, and infections with fungi on a spectrum of human pathogenicity can occur.Case ReportWe report a case of a 17‐year‐old lung transplant recipient in whom Irpex lacteus and Rhodotorula species were identified during surveillance bronchoscopy. She was asymptomatic and deemed to be colonized by Irpex lacteus and Rhodotorula species following transplant. 2 years after transplantation, she developed a fever, respiratory symptoms, abnormal lung imaging, and histological evidence of acute and chronic bronchitis on transbronchial biopsy. After developing symptoms concerning for a pulmonary infection and graft dysfunction, she was treated for a presumed IFD. Unfortunately, further diagnostic testing could not be performed at this time given her tenuous clinical status. Despite the initiation of antifungal therapy, her graft function continued to decline resulting in a second lung transplantation.ConclusionsThis case raises the concern for IFD in lung transplant recipients from Irpex species. Further investigation is needed to understand the pathogenicity of this organism, reduce the incidence and mortality of IFD in lung transplant recipients, and refine the approach to diagnosis and manage the colonization and isolation of rare, atypical fungal pathogens in immunocompromised hosts.
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
在一名小儿肺移植受者的监视支气管镜检查中鉴定出 Irpex 和 Rhodotorula:关于这些非典型真菌的病例报告和文献综述
背景侵袭性真菌病(IFD)是小儿肺移植受者的常见并发症,多达 12% 的患者在第一年就会发生。感染的风险因素包括肺部防御功能受损和强烈的免疫抑制疗法。虽然大多数 IFD 是由曲霉菌引起的,但其他真菌的分生孢子也会被不断吸入,因此也会发生与人类致病性有关的真菌感染。病例报告我们报告了一例 17 岁肺移植受者的病例,她在支气管镜监测中发现了乳酸伊尔佩克斯菌(Irpex lacteus)和Rhodotorula 菌。她在移植后无症状,被认为已被乳酸伊氏杆状病毒和罗氏杆状病毒定植。移植 2 年后,她出现了发烧、呼吸道症状、肺部影像异常以及经支气管活检的急慢性支气管炎组织学证据。在出现肺部感染和移植物功能障碍的症状后,她接受了假定的 IFD 治疗。遗憾的是,鉴于她的临床状况十分脆弱,目前无法进行进一步的诊断测试。尽管开始了抗真菌治疗,但她的移植物功能仍在继续下降,结果导致了第二次肺移植手术。需要进一步调查以了解这种生物的致病性,降低肺移植受者 IFD 的发病率和死亡率,并改进诊断和管理免疫功能低下宿主中罕见的非典型真菌病原体定植和分离的方法。
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
Pediatric Transplantation
Pediatric Transplantation 医学-小儿科
CiteScore
2.90
自引率
15.40%
发文量
216
审稿时长
3-8 weeks
期刊介绍: The aim of Pediatric Transplantation is to publish original articles of the highest quality on clinical experience and basic research in transplantation of tissues and solid organs in infants, children and adolescents. The journal seeks to disseminate the latest information widely to all individuals involved in kidney, liver, heart, lung, intestine and stem cell (bone-marrow) transplantation. In addition, the journal publishes focused reviews on topics relevant to pediatric transplantation as well as timely editorial comment on controversial issues.
期刊最新文献
Donor Characteristics and Outcomes of Pediatric Heart Transplantation in South Korea. Outcomes of Pediatric Liver Transplantation in Glycogen Storage Disease Type 1b-A Single-Center Experience. Cardiovascular Risk in Pediatric Renal Transplant Recipients. Liver Transplantation for Nijmegen Breakage Syndrome With Hepatic Malignancy and Hepatopulmonary Syndrome After Bone Marrow Transplantation: A Case Report. Pediatric Organ Donation: 16-Year Experience of PICU/ICU of a Third Level Hospital in Portugal, 2006-2021.
×
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