Okwechime Remi T, Reyes Nicholas, Trivedi Darshan, Iwuchukwu Ifeanyi O
Department of Neurocritical Care, Ochsner Clinic Foundation, New Orleans, LA.
The University of Queensland Medical School, Ochsner Clinical School, New Orleans, LA.
Ochsner J. 2022 Summer;22(2):169-175. doi: 10.31486/toj.21.0088.
Mucormycosis is a serious angioinvasive fungal infection. Immunocompromised patients are more likely to be susceptible to mucormycosis than immunocompetent individuals. Cerebral mucormycosis has been reported, but cases have primarily been unilateral. We report a case of bilateral cerebral mucormycosis in an immunocompetent patient. A 37-year-old female with no significant medical history was transferred to our tertiary center after cerebrospinal fluid profile following a lumbar puncture at an outside hospital suggested bacterial meningitis. Computed tomography of the head revealed hypodensity and cerebral edema in the left basal ganglia, and magnetic resonance imaging (MRI) brain showed increased T2 signal and mass-like configuration centered in the left basal ganglia. During her hospital stay, she had neurologic decompensation with respiratory failure. She was intubated and placed on mechanical ventilation. Repeat MRI brain revealed evolving cerebral edema signal and interval development of progression across the midline involving the right basal ganglia. Because of the aggressive nature of the lesion and cerebral edema, she underwent a biopsy with placement of an external ventricular drain. Despite medical and surgical interventions, she neurologically worsened and died. Histopathologic evaluation of the biopsied lesion revealed numerous fungal hyphae consistent with mucormycosis. Our patient was not immunocompromised, and this case highlights the clinical challenges in initiating immunosuppressive therapy in a patient with rapidly progressive central nervous system disease.
毛霉菌病是一种严重的血管侵袭性真菌感染。免疫功能低下的患者比免疫功能正常的个体更容易感染毛霉菌病。虽然已有脑毛霉菌病的报道,但病例主要为单侧。我们报告一例免疫功能正常患者的双侧脑毛霉菌病。一名37岁无显著病史的女性在外部医院腰椎穿刺后的脑脊液检查提示细菌性脑膜炎后被转诊至我们的三级医疗中心。头部计算机断层扫描显示左侧基底节区低密度影和脑水肿,脑部磁共振成像(MRI)显示T2信号增强,且以左侧基底节区为中心呈肿块样形态。在住院期间,她出现神经功能失代偿并伴有呼吸衰竭。她接受了气管插管并进行机械通气。复查脑部MRI显示脑水肿信号进展,且病变跨越中线发展累及右侧基底节区。由于病变的侵袭性和脑水肿,她接受了活检并放置了外置脑室引流管。尽管采取了药物和手术干预措施,她的神经功能仍恶化并最终死亡。对活检病变的组织病理学评估显示有大量符合毛霉菌病的真菌菌丝。我们的患者并非免疫功能低下,该病例凸显了在患有快速进展性中枢神经系统疾病的患者中启动免疫抑制治疗所面临的临床挑战。