A case of apparent ART-associated immune reconstitution inflammatory syndrome in a patient with Strongyloides stercoralis infection

Dwayvania Miller, Yassine Kilani, Ebehiwele Ebhohon, Emnet Keftassa, K. Hennessey, Addi Feinstein
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Abstract

Introduction: Strongyloides infection is most commonly caused by Strongyloides stercoralis (S. stercoralis). It often causes asymptomatic chronic infection but through the translocation of the parasite into the bloodstream, it can lead to disseminated strongyloidiasis (DS). We describe a case of a patient with human immunodeficiency virus (HIV) who developed Strongyloidiasis with the complication of vancomycin-resistant Enterococcus (VRE) meningitis. Notably, the clinical condition of the patient worsened after commencing anti-retroviral therapy (ART), raising concern for ART-associated immune reconstitution inflammatory syndrome (IRIS) to S. stercoralis. Case Report: A 51-year-old African female with a past medical history of HIV presented with a 1-week history of abdominal pain and a 2-month history of generalized malaise, constipation, and weight loss. She improved with symptomatic management and commenced Biktarvy. She re-presented one month later with worsening gastrointestinal symptoms. Her hospital course was complicated by septicemia with worsening mentation. Her repeat abdominal imaging showed ascending and transverse colitis and cerebrospinal fluid analysis was positive for vancomycin-resistant Enterococcus faecium (VRE). During her re-admission, the patient developed persistent watery diarrhea which was found to be positive for S. stercoralis. Despite medical therapy she demised on day 28 of admission. Conclusion: Literature is very scarce concerning the progression of S. stercoralis infection to Strongyloides disseminated strongyloidiasis (DS) as a result of IRIS. As clinicians, we must have a high index of suspicion in our HIV population as DS can lead to fatal complications. It can also help guide management decisions concerning ART until complete eradication of S. stercoralis infection is obtained.
粪类圆线虫感染患者出现明显的art相关免疫重建炎症综合征1例
导言:类圆线虫感染最常由粪圆线虫(S. stercoralis)引起。它通常引起无症状的慢性感染,但通过寄生虫易位进入血液,可导致播散性圆线虫病(DS)。我们描述了一例人类免疫缺陷病毒(HIV)患者发展为类圆线虫病,并发万古霉素耐药肠球菌(VRE)脑膜炎。值得注意的是,患者的临床状况在开始抗逆转录病毒治疗(ART)后恶化,引起了人们对抗逆转录病毒治疗相关免疫重建炎症综合征(IRIS)对粪球菌的关注。病例报告:51岁非洲女性,既往有HIV病史,腹痛1周,全身性不适、便秘和体重减轻2个月。她的症状得到改善,并开始Biktarvy。1个月后再次出现胃肠道症状恶化。她的住院过程因败血症和恶化的精神状态而复杂化。她的腹部重复成像显示上升性和横向结肠炎,脑脊液分析显示万古霉素耐药屎肠球菌(VRE)阳性。在她再次入院时,患者出现持续水样腹泻,发现粪球菌阳性。尽管接受了药物治疗,但她在入院第28天死亡。结论:关于粪链球菌感染由IRIS发展为播散性圆形线虫病(DS)的文献很少。作为临床医生,我们必须对我们的艾滋病毒人群有高度的怀疑指数,因为DS可能导致致命的并发症。它还可以帮助指导有关抗逆转录病毒治疗的管理决策,直到完全根除粪球菌感染。
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