Chen Chi-Tung, Ho Mao-Wang, Chung Wei-Hsin
Division of Cardiovascular Medicine, Department of Internal Medicine, China Medical University Hospital, Taichung, Taiwan.
Division of Infectious Disease, Department of Internal Medicine, China Medical University Hospital, Taichung, Taiwan.
BMC Infect Dis. 2024 Dec 18;24(1):1413. doi: 10.1186/s12879-024-10267-6.
Cryptococcosis is an opportunistic fungal infection in immunocompromised patients. The major species include Cryptococcus grubii, Cryptococcus neoformans, and rarely, Cryptococcus gattii. Here we present a disseminated Cryptococcus gattii infection in a patient with elevated granulocyte-macrophage colony-stimulating-factor autoantibody which was successfully treated with antifungal therapy.
A 61-year-old healthy man presented with a 3-week history of blurred vision, low-grade fever, headache, and a one-year history of low back pain following a fall on his farm. Physical examination revealed lower back tenderness and diplopia. He was tested negative for hepatitis B, C, and human immunodeficiency virus. Chest X-ray revealed a focal opacity in the right retrocardiac paraspinal region and pleural effusion. Magnetic resonance imaging showed a mass located at the L1 prevertebral region and multiple rim-enhancing lesions in bilateral cerebral hemispheres. Thoracoscopy demonstrated cystic lesions at the right costopleural angle. Pathology and microbiology studies confirmed the diagnosis of disseminated Cryptococcus gatti infection. Autoantibodies to granulocyte-macrophage colony-stimulating factor were detected and were considered to cause disseminated cryptococcosis. The patient was started on amphotericin B followed by fluconazole treatment. One month later, the symptoms ameliorated and repeated image studies after 1 year of follow-up showed the resolution of lesions.
This report describes the first case of disseminated Cryptococcus gattii infection involving the musculoskeletal system, respiratory system, and central nervous system with granulocyte-macrophage colony-stimulating-factor autoantibody by evidence of histology and microbiology.
隐球菌病是免疫功能低下患者的一种机会性真菌感染。主要菌种包括格特隐球菌、新生隐球菌,很少见的加氏隐球菌。在此,我们报告一例伴有粒细胞-巨噬细胞集落刺激因子自身抗体升高的播散性加氏隐球菌感染患者,该患者经抗真菌治疗后成功治愈。
一名61岁健康男性,有3周视力模糊、低热、头痛病史,以及在农场摔倒后出现的1年腰痛病史。体格检查发现下背部压痛和复视。他的乙肝、丙肝和人类免疫缺陷病毒检测均为阴性。胸部X线显示右心后椎旁区域有局灶性模糊影及胸腔积液。磁共振成像显示L1椎体前区域有一肿块,双侧大脑半球有多个环形强化病灶。胸腔镜检查发现右侧肋膈角有囊性病变。病理和微生物学研究确诊为播散性加氏隐球菌感染。检测到粒细胞-巨噬细胞集落刺激因子自身抗体,认为其导致了播散性隐球菌病。患者开始接受两性霉素B治疗,随后用氟康唑治疗。1个月后症状改善,随访1年后重复影像学检查显示病灶消退。
本报告通过组织学和微生物学证据描述了首例累及肌肉骨骼系统、呼吸系统和中枢神经系统的伴有粒细胞-巨噬细胞集落刺激因子自身抗体的播散性加氏隐球菌感染病例。