Niño Oberto S, Ponce de León A, Sierra Madero J
Departamento de infectología, Instituto Nacional de la Nutrición Salvador Zubirán.
Rev Invest Clin. 1999 Jan-Feb;51(1):43-8.
A case of primary coccidiodal meningitis without pulmonary, osseous or dermic affection due to Coccidioides immitis in a 27 years old male patient with hypertensive brain of one month of evolution, was reported. The patient was resident of Northern California, and he was previously healthy. The cerebrospinal fluid (CSF) showed a glucose of 22 mg/dL, proteins 62 mg/dL, white blood cells 100/mm3 (97% PMN, 3% MN). CT SCAN showed bilateral ventricular dilatation. Diagnosis of coccidioidal meningitis was made based on antibodies against anticoccidioides (IgM 6.8 mg/dL and IgG 4.9 mg/dL, normal < 2 mg/dL) and growth of Coccidioides immitis. The chest radiograph was normal and the detection of antibodies against human immunodeficiency virus was negative. A VP shunt was placed and the patient was treated with intravenous amphotericin B and intratecal amphotericin B through on Ommaya reservoir. Even with antifungal treatment the patient deteriorated neurologically after an initial transient improvement, he died two weeks later in his hometown.
报告了一例原发性球孢子菌性脑膜炎病例,患者为一名27岁男性,患有病程1个月的高血压脑病,无肺部、骨骼或皮肤感染,由粗球孢子菌引起。该患者居住在北加利福尼亚,既往健康。脑脊液显示葡萄糖22mg/dL,蛋白质62mg/dL,白细胞100/mm³(97%中性粒细胞,3%单核细胞)。CT扫描显示双侧脑室扩张。基于抗球孢子菌抗体(IgM 6.8mg/dL和IgG 4.9mg/dL,正常<2mg/dL)以及粗球孢子菌的生长情况,诊断为球孢子菌性脑膜炎。胸部X光片正常,人类免疫缺陷病毒抗体检测为阴性。放置了脑室腹腔分流管,并通过Ommaya储液器对患者进行静脉注射两性霉素B和鞘内注射两性霉素B治疗。尽管进行了抗真菌治疗,但患者在最初短暂改善后神经功能仍恶化,两周后在家乡去世。