一名人类免疫缺陷病毒感染者在感染血吸虫病后迅速出现神经系统感染:病例报告

iLABMED Pub Date : 2024-07-22 DOI:10.1002/ila2.54
Yan Liu, Guoqiang Zhou, Wei Jiang, Xianglong Kong
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引用次数: 0

摘要

HIV-1 和血吸虫感染给全球健康带来了巨大挑战,而这些病原体的神经系统表现因其罕见性很容易被误诊。在此,我们报告了一例 36 岁获得性免疫缺陷综合征患者的病例,该患者在 4 年前被初步诊断为人类免疫缺陷病毒-1(HIV-1)感染,但在结核病诊断和住院治疗后开始接受抗逆转录病毒疗法(ART)之前的大约 3 年里一直未接受治疗。尽管在抗逆转录病毒疗法后 1 年,HIV-1 病毒得到了抑制,但他因高烧和头痛再次入院。根据临床表现和脑部影像学特征对疑似结核病的初步治疗失败,进一步检查证实是血吸虫病引起的颅内感染。经过抗血吸虫治疗和优化的抗逆转录病毒疗法,患者完全康复出院。这例感染了人类免疫缺陷病毒(HIV)的亚洲患者在感染血吸虫病后迅速发展为神经系统感染的病例突出表明,HIV 感染者需要了解此类合并感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid development of neurological infection in a patient with human immunodeficiency virus following schistosomiasis: A case report
HIV‐1 and schistosomal infections present significant global health challenges, and neurological manifestations of these pathogens are easily misdiagnosed due to their rarity. Here, we report the case of a 36‐year‐old patient with acquired immunodeficiency syndrome who was initially diagnosed with human immunodeficiency virus‐1 (HIV‐1) infection 4 years earlier, although untreated for approximately 3 years until he began antiretroviral therapy (ART) following a tuberculosis diagnosis and hospitalization. Despite achieving virological suppression of HIV‐1 1 year after ART, he was readmitted with high fever and headache. Initial therapy for suspected tuberculosis based on clinical performance and brain imaging features failed, and further investigation confirmed an intracranial infection caused by schistosomiasis. Following anti‐schistosomal treatment and optimized ART, the patient recovered fully and was discharged. This case of a patient in Asia infected with human immunodeficiency virus (HIV) who rapidly developed a neurological infection subsequent to acquiring schistosomiasis highlights the need for awareness of such coinfections in patients with HIV.
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