Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bld 10, Rm 11C208, 9000 Rockville Pike, Bethesda, MD, 20892, USA.
Division of Infectious Diseases, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA, USA.
J Clin Immunol. 2021 Apr;41(3):545-551. doi: 10.1007/s10875-020-00954-9. Epub 2021 Jan 2.
We present a case of central nervous system (CNS) histoplasmosis in a previously healthy adult with hepatitis C (HCV) presenting with neurological symptoms refractory to antifungal therapy and ventriculoperitoneal (VP) shunting 4 months after initial diagnosis. Persistent symptoms were thought to be inflammatory rather than infectious given negative cerebrospinal fluid (CSF) and serum fungal antigens. The patient promptly improved after initiation of corticosteroid therapy. Elevated CSF cytokines and regional enhancement on brain MRI resolved with corticosteroid treatment. This is the first case of Histoplasma-associated post-infectious inflammatory response syndrome (Histo-PIIRS) documented by CSF cytokine reduction in response to corticosteroid therapy.
我们报告了一例中枢神经系统(CNS)组织胞浆菌病病例,患者为既往健康的丙型肝炎(HCV)成人,在初始诊断后 4 个月出现神经症状,对抗真菌治疗无反应,并进行了脑室-腹腔(VP)分流。鉴于脑脊液(CSF)和血清真菌抗原均为阴性,持续性症状被认为是炎症性而非感染性。鉴于患者对皮质类固醇治疗反应迅速,因此推测患者的症状是由炎症反应而非感染引起的。在开始皮质类固醇治疗后,患者的症状迅速改善。脑 MRI 上的 CSF 细胞因子升高和区域性增强在皮质类固醇治疗后得到缓解。这是首例通过 CSF 细胞因子减少对皮质类固醇治疗有反应而确诊的组织胞浆菌相关性感染后炎症反应综合征(Histo-PIIRS)病例。