Merkler Alexander E, Gaines Nathan, Baradaran Hediyeh, Schuetz Audrey N, Lavi Ehud, Simpson Sara A, Dinkin Marc J
Department of Neurology, Weill Cornell Medical College, New York, NY, USA.
Department of Radiology, Weill Cornell Medical College, New York, NY, USA.
Neurohospitalist. 2015 Oct;5(4):217-22. doi: 10.1177/1941874415569072.
Cryptococcus spp is a common fungal infection and frequent cause of meningitis in immunocompromised patients; however, immunocompetent patients are also at risk of infection. Visual loss often occurs via elevated intracranial hypertension but can rarely occur through direct optic nerve, chiasm, or tract invasion. We report a case of a 38-year-old woman who presented with decreased acuity in both eyes. She had generalized visual field constriction in the right eye and temporal hemianopsia in the left eye. Magnetic resonance imaging of the brain and orbits showed multiple areas of ill-defined enhancement in the optic chiasm and tracts as well as in the diaphragmatic sella, prepontine and interpeduncular cisterns, and along cranial nerves VI, VII, and VIII bilaterally. Initial cerebrospinal fluid (CSF) showed 34 white blood cells, hypoglycorrhachia, and negative cryptococcal antigen and bacterial and fungal cultures. A transphenoidal biopsy of the dura and pituitary gland was unremarkable. Empiric steroids resulted in marked improvement in visual acuity in both eyes, but while tapering steroids, she developed rapid visual loss bilaterally. Repeat CSF performed 6 weeks later demonstrated a cryptococcal antigen titer of 1:512. Retroactive staining of the pituitary biopsy was positive for mucicarmine, a component of the polysaccharide capsule of Cryptococcus spp. After induction therapy with amphotericin B and flucytosine and 1 year of fluconazole, her visual acuity was 20/20 in both eyes. In summary, Cryptococcus can affect immunocompetent patients and often presents with insidious, chronic meningitis. Visual loss is common in cryptococcal meningitis but usually results from fulminant papilledema related to elevated intracranial pressure. In rare cases, direct nerve or chiasm infiltration by the fungus results in vision loss.
隐球菌属是一种常见的真菌感染,也是免疫功能低下患者患脑膜炎的常见原因;然而,免疫功能正常的患者也有感染风险。视力丧失通常是由于颅内压升高引起的,但很少是通过直接侵犯视神经、视交叉或视束导致的。我们报告一例38岁女性患者,其双眼视力下降。右眼有全视野缩小,左眼有颞侧偏盲。脑部和眼眶的磁共振成像显示视交叉、视束以及鞍膈、脑桥前池和脚间池,还有双侧第六、七、八对脑神经处有多个边界不清的强化区域。最初的脑脊液检查显示有34个白细胞、脑脊液低糖,隐球菌抗原、细菌和真菌培养均为阴性。经蝶窦对硬脑膜和垂体进行活检,结果无异常。经验性使用类固醇后,双眼视力有明显改善,但在逐渐减少类固醇用量时,她双眼视力迅速丧失。6周后复查脑脊液,隐球菌抗原滴度为1:512。垂体活检的追溯染色显示黏卡红染色阳性,黏卡红是隐球菌属多糖荚膜的一种成分。在用两性霉素B和氟胞嘧啶进行诱导治疗以及1年的氟康唑治疗后,她双眼视力恢复到20/20。总之,隐球菌可感染免疫功能正常的患者,常表现为隐匿性慢性脑膜炎。视力丧失在隐球菌性脑膜炎中很常见,但通常是由与颅内压升高相关的暴发性视乳头水肿导致的。在罕见情况下,真菌直接侵犯神经或视交叉会导致视力丧失。