Kenaya Nikolas, Hermiz Joshua, Hailo Joshua, Chehab Zahra, Johnson Emelia, Toquica Gahona Christian, Asif Saba
Department of Internal Medicine, Wayne State University School of Medicine, Trinity Health Oakland Hospital, Pontiac, USA.
Department of Internal Medicine, Wayne State University School of Medicine, Detroit Medical Center, Detroit, USA.
Eur J Case Rep Intern Med. 2025 Aug 13;12(9):005604. doi: 10.12890/2025_005604. eCollection 2025.
Invasive central nervous system (CNS) aspergillosis is rare among human immunodeficiency virus (HIV)-positive patients due to preserved neutrophil function, despite significant CD4+ T-cell depletion. Diagnosis typically requires histopathologic confirmation, but polymerase chain reaction (PCR) testing has introduced new challenges due to its high sensitivity but limited specificity.
We describe a newly diagnosed 43-year-old HIV-positive male with concurrent Hodgkin lymphoma who presented with progressive neurological decline and a ring-enhancing brain lesion. While histopathological analysis of the brain biopsy demonstrated features of HIV-associated leukoencephalopathy, PCR testing paradoxically identified ; however, histopathological examination failed to demonstrate definitive fungal elements. Despite negative cerebrospinal fluid galactomannan and β-D-glucan assays, empiric voriconazole therapy was initiated in accordance with current treatment guidelines. Over the ensuing month, the patient returned with worsening neurologic status, radiographic lesion progression, and ultimately developed Torsades de Pointes, and multiorgan failure, resulting in death.
This case underscores the diagnostic and therapeutic complexities of PCR-positive, histopathology-negative CNS aspergillosis in HIV. Overreliance on molecular results without confirmatory pathology may lead to unnecessary antifungal therapy and severe drug toxicity. Additionally, overlapping immunosuppressive conditions-such as HIV and lymphoma-complicate clinical interpretation and management.
In HIV-positive patients with CNS lesions, PCR detection of should not independently justify antifungal therapy. Histological confirmation and multidisciplinary evaluation are essential to avoid misdiagnosis and adverse outcomes. This case highlights the urgent need for more precise treatment guidelines on when to initiate and discontinue antifungal treatment in complex immunocompromised populations.
Polymerase chain reaction positivity for in the absence of histopathologic confirmation presents a major diagnostic dilemma, particularly in human immunodeficiency virus (HIV)-positive patients, where overreliance on molecular diagnostics may lead to misdiagnosis, unnecessary antifungal exposure, and significant toxicity.Empiric antifungal treatment should be re-evaluated when central nervous system lesions progress or fail to improve, as prolonged use of agents like voriconazole can result in serious toxicity, including arrhythmias like Torsades de Pointes; clearer guidelines are needed to define when empiric treatment is appropriate in complex cases.HIV-positive patients with coexisting malignancy require a multidisciplinary, evidence-based approach, as overlapping immunosuppressive conditions can obscure diagnosis and complicate treatment decisions.
侵袭性中枢神经系统(CNS)曲霉病在人类免疫缺陷病毒(HIV)阳性患者中较为罕见,尽管CD4+T细胞显著耗竭,但中性粒细胞功能得以保留。诊断通常需要组织病理学确认,但聚合酶链反应(PCR)检测因其高敏感性但有限的特异性带来了新的挑战。
我们描述了一名新诊断的43岁HIV阳性男性,同时患有霍奇金淋巴瘤,表现为进行性神经功能衰退和脑环形强化病变。虽然脑活检的组织病理学分析显示了HIV相关白质脑病的特征,但PCR检测却意外地发现了[此处原文缺失相关内容];然而,组织病理学检查未能发现明确的真菌成分。尽管脑脊液半乳甘露聚糖和β - D - 葡聚糖检测呈阴性,但根据当前治疗指南仍开始了经验性伏立康唑治疗。在随后的一个月里,患者神经状态恶化、影像学病变进展,最终出现尖端扭转型室速和多器官功能衰竭,导致死亡。
本病例强调了HIV患者中PCR阳性、组织病理学阴性的CNS曲霉病的诊断和治疗复杂性。过度依赖分子检测结果而无病理确认可能导致不必要的抗真菌治疗和严重的药物毒性。此外,如HIV和淋巴瘤等重叠的免疫抑制状况会使临床解读和管理变得复杂。
在HIV阳性且有CNS病变的患者中,PCR检测到[此处原文缺失相关内容]不应单独作为抗真菌治疗的依据。组织学确认和多学科评估对于避免误诊和不良后果至关重要。本病例凸显了迫切需要针对复杂免疫受损人群何时开始及停止抗真菌治疗制定更精确的治疗指南。
在缺乏组织病理学确认的情况下,PCR检测呈阳性存在重大诊断困境,尤其是在人类免疫缺陷病毒(HIV)阳性患者中,过度依赖分子诊断可能导致误诊、不必要的抗真菌暴露和显著毒性。当中枢神经系统病变进展或无改善时,应重新评估经验性抗真菌治疗,因为长期使用伏立康唑等药物可能导致严重毒性,包括尖端扭转型室速等心律失常;需要更明确的指南来界定在复杂病例中何时进行经验性治疗是合适的。合并恶性肿瘤的HIV阳性患者需要多学科、基于证据的方法,因为重叠的免疫抑制状况会模糊诊断并使治疗决策复杂化。