Division of Pediatric Infectious Diseases, Chang Gung University, Kweishan, Taoyuan, Taiwan.
Pediatr Neurol. 2010 Apr;42(4):267-70. doi: 10.1016/j.pediatrneurol.2009.10.015.
Between 1991-2006, nine patients below age 18 years, with a microbiologic documentation of Cryptococcus neoformans infection and no evidence of human immunodeficiency virus infection, were identified and treated at Chang Gung Children's Hospital. All exhibited central nervous system involvement. Seven patients were female (age range, 9-16 years; mean age, 13.7 years). Five patients (56%) manifested underlying diseases and were receiving either steroid or immunosuppressant treatment at time of disease onset. Eight patients presented with meningitis. Headache, vomiting, and focal neurologic signs were the most common presentations. Protein and sugar levels in cerebrospinal fluid were within normal range in seven cases, whereas India ink smear and cryptococcal antigen testing were positive in 87% (7/8) and 78% (7/9) of patients, respectively. With prompt antifungal therapy, all survived, but one presented the sequel of blindness. Cryptococcosis is uncommon in the nonhuman immunodeficiency virus-infected pediatric population. Clinicians should take into account a diagnosis of central nervous system cryptococcosis when children present with prolonged headache, vomiting, and focal neurologic signs. Indian ink stain and cryptococcal antigen testing of cerebrospinal fluid should be performed.
1991-2006 年间,在长庚儿童医学中心共发现并治疗了 9 例年龄在 18 岁以下、微生物学证明为新型隐球菌感染且无人类免疫缺陷病毒感染证据的患者。所有患者均有中枢神经系统受累。7 例为女性(年龄 9-16 岁;平均年龄 13.7 岁)。5 例(56%)有基础疾病,在发病时正在接受类固醇或免疫抑制剂治疗。8 例表现为脑膜炎。头痛、呕吐和局灶性神经体征是最常见的表现。7 例患者的脑脊液蛋白和糖水平均在正常范围内,而印度墨水涂片和隐球菌抗原检测的阳性率分别为 87%(7/8)和 78%(7/9)。在及时进行抗真菌治疗后,所有患者均存活,但 1 例患者出现失明后遗症。新型隐球菌病在非人类免疫缺陷病毒感染的儿科人群中并不常见。当儿童出现持续性头痛、呕吐和局灶性神经体征时,临床医生应考虑中枢神经系统隐球菌病的诊断。应进行脑脊液印度墨水染色和隐球菌抗原检测。