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获得性免疫缺陷综合征患者抗真菌治疗后出现非典型矛盾性炎症反应的隐球菌性脑膜炎:一例报告

Cryptococcal meningitis with atypical paradoxical inflammatory reactions after antifungal treatment in acquired immune deficiency syndrome: A case report.

作者信息

Samukawa Sei, Yoshimi Ryusuke, Kojitani Noriko, Uzawa Yuji, Takase-Minegishi Kaoru, Kirino Yohei, Soejima Yutaro, Kato Hideaki, Nakajima Hideaki

机构信息

Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.

Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.

出版信息

J Infect Chemother. 2023 Mar;29(3):347-352. doi: 10.1016/j.jiac.2022.11.002. Epub 2022 Nov 13.

Abstract

Cryptococcal meningitis (CM) is a life-threatening disease that primarily affects patients with human immunodeficiency virus (HIV). Antifungal therapy with antiretroviral treatment (ART) usually leads to the clinical remission of CM; however, in some cases, these treatments exacerbate intracranial inflammation because of paradoxical inflammatory reaction or immune reconstitution inflammatory syndrome (IRIS). Here we report two CM cases that presented atypical clinical courses attributed to paradoxical inflammatory reactions. The first case was a 43-year-old man with headache and vertigo diagnosed with CM and HIV. The patient's CM not only was refractory to the antifungal combination therapy of liposomal amphotericin B (L-AMB) and fluconazole (FLCZ) but suddenly worsened because of a paradoxical inflammatory reaction after 18 days of treatment. He passed away from brain herniation on day 23. The second case was a 43-year-old man diagnosed with CM and HIV. After receiving antifungal therapy and ART, the patient's status was stable for more than 3 years with undetectable HIV-RNA. He suddenly presented with brain inflammation and was diagnosed with IRIS due to CM (CM-IRIS). His brain lesions were migratory and refractory to various antifungal therapies such as L-AMB, FLCZ, flucytosine, and intrathecal amphotericin B. Although the cryptococcal antigen in the patient's cerebrospinal fluid gradually diminished after continuous antifungal therapies, his cognitive function declined, and right hemiparesis persisted. These two cases of CM presented atypical clinical courses, presumably because of paradoxical inflammatory reactions. It should be noted that the onset of CM-IRIS may not necessarily depend on the timing of ART initiation.

摘要

隐球菌性脑膜炎(CM)是一种危及生命的疾病,主要影响人类免疫缺陷病毒(HIV)感染者。抗真菌治疗联合抗逆转录病毒治疗(ART)通常可使CM临床缓解;然而,在某些情况下,这些治疗会因反常炎症反应或免疫重建炎症综合征(IRIS)而加剧颅内炎症。在此,我们报告两例因反常炎症反应导致非典型临床病程的CM病例。第一例是一名43岁男性,有头痛和眩晕症状,被诊断为CM和HIV。该患者的CM不仅对脂质体两性霉素B(L-AMB)和氟康唑(FLCZ)的抗真菌联合治疗无效,而且在治疗18天后因反常炎症反应突然恶化。他在第23天因脑疝去世。第二例是一名43岁男性,被诊断为CM和HIV。接受抗真菌治疗和ART后,患者病情稳定超过3年,HIV-RNA检测不到。他突然出现脑部炎症,被诊断为CM相关的IRIS(CM-IRIS)。他的脑部病变呈游走性,对多种抗真菌治疗如L-AMB、FLCZ、氟胞嘧啶和鞘内注射两性霉素B均无效。尽管在持续抗真菌治疗后患者脑脊液中的隐球菌抗原逐渐减少,但他的认知功能下降,右侧偏瘫持续存在。这两例CM呈现非典型临床病程,可能是由于反常炎症反应所致。需要注意的是,CM-IRIS的发作不一定取决于开始ART的时间。

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