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未诊断的新型隐球菌性脑膜炎导致正常压力脑积水患者出现随后的脑室-腹腔分流感染:病例报告及文献复习。

Undiagnosed Cryptococcus gattii meningitis leading to subsequent ventriculoperitoneal shunt infection in a patient with symptoms of normal pressure hydrocephalus: case report and literature review.

机构信息

Division of Infectious Diseases and Tropical Medicine, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, 2 Wanglang Road, Bangkoknoi, Bangkok, 10700, Thailand.

Department of Microbiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

出版信息

BMC Infect Dis. 2018 Jun 4;18(1):257. doi: 10.1186/s12879-018-3165-y.

Abstract

BACKGROUND

Cryptococcus gattii is known to be an etiologic agent of human cryptococcosis, particularly in immunocompetent persons. C. gattii infection usually involves the central nervous system, the respiratory tract, or may be disseminated. Here we report an atypical manifestation of C. gattii infection in a patient who had C. gattii meningitis complicating the ventriculoperitoneal (VP) shunt infection and concurrent infected intraabdominal VP shunt pseudocyst.

CASE PRESENTATION

A 66-year-old Thai female was initially diagnosed with normal pressure hydrocephalus (NPH) and underwent programmable VP shunt placement. However, she still suffered from recurrent communicating hydrocephalus with in-place VP shunt, and later developed recurrent gait impairment, chronic abdominal pain and abdominal mass. Radiological studies demonstrated recurrent hydrocephalus and a very large intraabdominal VP shunt pseudocyst. C. gattii was isolated from both the cerebrospinal fluid and the pseudocyst aspiration. C. gattii meningitis complicating the VP shunt infection and concurrent infected intraabdominal VP shunt pseudocyst was diagnosed. Prolonged antifungal therapy, removal of the infected VP shunt with subsequent implant of a new shunt provided a good outcome.

CONCLUSION

Chronic C. gattii meningitis should be aware in a patient presenting with normal pressure hydrocephalus. Under-diagnosed cryptococcal meningitis following VP shunt insertion for treating the hydrocephalus can render a complicated VP shunt infection including infected VP shunt pseudocyst.

摘要

背景

新型隐球菌已知是人类隐球菌病的病原体,尤其在免疫功能正常者中。新型隐球菌感染通常涉及中枢神经系统、呼吸道,或可能播散。在此,我们报告一例新型隐球菌感染的非典型表现,患者有新型隐球菌性脑膜炎合并脑室-腹腔(VP)分流感染和并发感染性腹腔内 VP 分流假性囊肿。

病例介绍

一名 66 岁泰国女性最初被诊断为正常压力脑积水(NPH)并接受可编程 VP 分流术。然而,她仍患有复发性交通性脑积水伴 VP 分流在位,后来出现复发性步态障碍、慢性腹痛和腹部肿块。影像学研究显示复发性脑积水和非常大的腹腔内 VP 分流假性囊肿。从脑脊液和假性囊肿抽吸物中均分离出新型隐球菌。诊断为新型隐球菌性脑膜炎合并 VP 分流感染和并发感染性腹腔内 VP 分流假性囊肿。延长抗真菌治疗,去除感染的 VP 分流并随后植入新的分流,获得了良好的结果。

结论

对于表现为正常压力脑积水的患者,应注意慢性新型隐球菌性脑膜炎。在为治疗脑积水而插入 VP 分流后,隐球菌性脑膜炎诊断不足会导致复杂的 VP 分流感染,包括感染性 VP 分流假性囊肿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e1a/5987493/4fdb4cf3ea61/12879_2018_3165_Fig1_HTML.jpg

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