Strongyloides stercoralis Dissemination and Hyperinfection Associated with Long-Term Steroid Treatment in a Neurosurgical Population.

IF 1 Q4 INFECTIOUS DISEASES
Mariana Constante, João Domingos, Francisco Neves Coelho, Teresa Baptista Fernandes, Teresa Baptista, Marta Maio Herculano
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Abstract

Strongyloidiasis develops from the infection with Strongyloides stercoralis (Family: Strongylidae) and was recently considered a neglected tropical disease by the World Health Organization due to its global distribution and high burden of infection. Here, we present the cases of two patients under corticosteroid therapy after neurosurgical surgery who developed septic shock-like hyperinfection syndrome due to disseminated strongyloidiasis. The first case is a 77-year-old man from Cape Verde who was diagnosed with an extra-axial right parietal brain mass. He was given dexamethasone and was submitted to a biparietal craniotomy. His condition deteriorated and he was admitted to the intensive care unit (ICU), where he was diagnosed with disseminated strongyloidiasis with hyperinfection. Anthelmintic treatment and corticosteroid therapy were rapidly tapered and stopped. Neurological dysfunction persisted and the patient was transferred to the ward. The patient had died after complications of hospital-acquired pneumonia. The second case is a 47-year-old man from Guinea-Bissau who was diagnosed with a space-occupying lesion in the right temporal region and started treatment with dexamethasone. He underwent a craniectomy with partial excision of the lesion (high-grade glioma). Later his neurologic state worsened, and he was diagnosed with septic shock and hospital-acquired pneumonia. He was admitted to the ICU, the diagnosis of disseminated strongyloidiasis and hyperinfection syndrome was made and he initiated treatment with ivermectin and albendazole. Corticosteroid therapy was tapered. The patient's clinical status deteriorated, and multiple opportunistic infections were diagnosed during the ICU stay, which lead him to die. Clinicians should have a high index of suspicion when in the presence of corticosteroid-treated patients with sepsis. Preventive strategies and subsequent treatment should be considered in patients with a risk of acquisition or dissemination. Treating severe strongyloidiasis is still a clinical challenge and a delayed diagnosis can significantly worsen the outcomes of the patients affected, as seen in the presented cases.

Abstract Image

Abstract Image

神经外科人群长期类固醇治疗与粪圆线虫传播和过度感染相关。
圆形线虫病是由粪形圆形线虫(圆形线虫科)感染发展而来,由于其全球分布和感染负担高,最近被世界卫生组织认为是一种被忽视的热带病。在此,我们报告了两例神经外科手术后接受皮质类固醇治疗的患者,由于播散性圆线虫病而出现脓毒性休克样过度感染综合征。第一个病例是一名来自佛得角的77岁男子,他被诊断为右脑顶叶轴外肿块。他被给予地塞米松,并提交了双顶骨开颅术。他的病情恶化,被送进重症监护病房(ICU),在那里他被诊断为播散性圆线虫病伴过度感染。驱虫药治疗和皮质类固醇治疗迅速逐渐减少并停止。神经功能障碍持续存在,患者被转移到病房。患者死于医院获得性肺炎并发症。第二个病例是来自几内亚比绍的一名47岁男子,他被诊断为右侧颞区占位性病变,并开始使用地塞米松治疗。他接受了部分切除病变(高级别胶质瘤)的颅骨切除术。后来他的神经状态恶化,他被诊断为感染性休克和医院获得性肺炎。他住进ICU,诊断为播散性圆线虫病和过度感染综合征,并开始伊维菌素和阿苯达唑治疗。皮质类固醇治疗逐渐减少。患者临床状况恶化,在ICU住院期间多次出现机会性感染,导致患者死亡。临床医生应该有高度的怀疑指数时,在存在皮质类固醇治疗的患者败血症。对于有感染或传播风险的患者,应考虑预防策略和后续治疗。治疗严重的圆线虫病仍然是一项临床挑战,如所述病例所示,延迟诊断可显著恶化受影响患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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