Mathews Marlon, Paré Laura, Hasso Anton
Department of Neurosurgery, University of California, Irvine, Orange, CA 92868.
Surg Neurol. 2007 Jun;67(6):647-9. doi: 10.1016/j.surneu.2006.10.049.
Cryptococcal infections of the CNS are infrequent in immunocompetent hosts. When present, they usually present as meningitis and hydrocephalus or as fungal masses called cryptococcomas. We report a case in which intraventricular cryptococcal cysts clinically and radiologically simulated the racemose form of neurocysticercosis.
A 23-year-old man presented to the emergency department with a 1-week history of severe headache, dizziness, nausea, vomiting, and some lethargy. A computed tomography scan revealed significant hydrocephalus. The patient was admitted to the hospital and immediately underwent a right ventriculostomy tube placement. CSF examination showed a meningitic pattern. Magnetic resonance imaging, including FLAIR images, showed multiple large cysts in the temporal horns of both lateral ventricles in addition to hydrocephalus. When an endoscopic left temporal cyst fenestration failed to decompress his trapped right temporal horn, he underwent placement of a left lateral ventricle to peritoneal shunt and a right temporal cyst to peritoneal shunt. ELISA test results for HIV-1 and -2 antibodies in the patient's serum were negative. His CD4 and CD8 counts were within normal limits. Multiple tests for CSF anticysticercal antibody using IgG ELISA gave unequivocally negative results. Latex agglutination tests detected Cryptococcus neoformans antigen in his CSF in titers of 1:1024, which progressively decreased in response to antifungal therapy. The patient underwent treatment with IV amphotericin B for 7 weeks, IV 5-FC for 2 weeks, and oral fluconazole for 5 weeks. At discharge, 3 consecutive CSF cultures were negative for bacteria and fungi. His neurologic status returned to baseline.
Cryptococcal CNS infections in immunocompetent hosts can mimic the intraventricular form of racemose neurocysticercosis. Distinguishing between the two is essential because the medical management of the 2 conditions is distinct from each other.
中枢神经系统隐球菌感染在免疫功能正常的宿主中并不常见。一旦出现,通常表现为脑膜炎和脑积水,或表现为称为隐球菌瘤的真菌团块。我们报告一例病例,其中脑室内隐球菌囊肿在临床和放射学上模拟了葡萄状神经囊尾蚴病。
一名23岁男性因严重头痛、头晕、恶心、呕吐及轻度嗜睡1周就诊于急诊科。计算机断层扫描显示严重脑积水。患者入院后立即接受了右心室造瘘管置入术。脑脊液检查显示为脑膜炎模式。包括液体衰减反转恢复序列(FLAIR)图像在内的磁共振成像显示,除脑积水外,双侧侧脑室颞角有多个大囊肿。当内镜下左侧颞叶囊肿开窗术未能缓解其被困的右侧颞角压力时,他接受了左侧脑室至腹膜分流术和右侧颞叶囊肿至腹膜分流术。患者血清中HIV-1和-2抗体的酶联免疫吸附测定(ELISA)结果为阴性。其CD4和CD8细胞计数在正常范围内。使用IgG ELISA对脑脊液抗囊尾蚴抗体进行的多次检测结果均明确为阴性。乳胶凝集试验在其脑脊液中检测到新型隐球菌抗原,滴度为1:1024,随着抗真菌治疗,滴度逐渐降低。患者接受了7周的静脉注射两性霉素B、2周的静脉注射5-氟胞嘧啶(5-FC)和5周的口服氟康唑治疗。出院时,连续3次脑脊液培养细菌和真菌均为阴性。他的神经状态恢复到基线水平。
免疫功能正常宿主的隐球菌中枢神经系统感染可模拟葡萄状神经囊尾蚴病的脑室内形式。区分这两种疾病至关重要,因为这两种情况的医疗管理截然不同。