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cryptococcus 心内膜炎:病例报告及文献复习。

Cryptococcus endocarditis: A case report and review of the literature.

机构信息

Division of General Internal Medicine, Akashi Medical Center, 743-33, Okubocho-Yagi, Akashi City, Hyogo, 674-0063, Japan.

Department of General Internal Medicine, Osaka General Medical Center, 3-1-56, Mandai-Higashi, Sumiyoshi-ku, Osaka, 558-8558, Japan.

出版信息

J Infect Chemother. 2019 Nov;25(11):901-905. doi: 10.1016/j.jiac.2019.05.003. Epub 2019 Jun 8.

Abstract

INTRODUCTION

Cryptococcus neoformans is known to be a cause of meningitis. However, as cryptococcal endocarditis is rare, it is not well understood. Here, we describe a case with Implantable Cardioverter Defibrillator associated endocarditis and meningitis caused by Cryptococcus neoformans and we review the literature associated cryptococcal endocarditis.

CASE PRESENTATION

A 72 years old Japanese male presented in emergency department with non-productive cough and respiratory discomfort. His past medical history was ischemic heart disease four years ago and ICD was implanted. Physical examination was unremarkable. Chest computer tomography revealed ground glass opacity in the right lung. He received a diagnosis of amiodarone-induced interstitial pneumonitis and high dose steroid pulse therapy. Septic shock and acute respiratory failure occurred after steroid therapy. Cryptococcus neoformans was identified by blood culture and cerebral spinal fluid. Intravenous liposomal Amphotericin B and oral flucytosine were initiated. Transesophageal echocardiography revealed vegetation on the lead of the ICD. Diagnosis of cryptococcal endocarditis was made. The patient died despite antifungal therapy was continued.

DISCUSSION

We analyzed our case and 8 cases of cryptococcal endocarditis in the literature for 40 years. Almost all of the patients had previous valve replacement surgery or immunocompromised state. Three cases had meningitis. Surgery performed in 3 cases. The overall mortality rate were 44.4%.

CONCLUSIONS

Cryptococcal endocarditis is rare and carries a high mortality. Almost all of the patients had underlying diseases. Diagnosis needs repeating blood culture and echocardiogram, sometimes. Cryptococcal endocarditis needs lumber puncture for rule out meningitis.

摘要

介绍

新型隐球菌已知可引起脑膜炎。然而,由于隐球菌性心内膜炎罕见,因此尚未得到充分了解。在这里,我们描述了一例与植入式心脏复律除颤器相关的心内膜炎和脑膜炎的病例,由新型隐球菌引起,并回顾了相关的隐球菌性心内膜炎文献。

病例介绍

一名 72 岁的日本男性因干咳和呼吸不适到急诊科就诊。他的既往病史为四年前的缺血性心脏病和 ICD 植入。体格检查无明显异常。胸部计算机断层扫描显示右肺磨玻璃样混浊。他被诊断为胺碘酮诱导的间质性肺炎,并接受了大剂量皮质类固醇脉冲治疗。皮质类固醇治疗后出现感染性休克和急性呼吸衰竭。血液培养和脑脊液中鉴定出新型隐球菌。开始静脉注射脂质体两性霉素 B 和口服氟胞嘧啶。经食管超声心动图显示 ICD 导线上有赘生物。诊断为隐球菌性心内膜炎。尽管继续抗真菌治疗,患者仍死亡。

讨论

我们分析了我们的病例和 40 年来文献中的 8 例隐球菌性心内膜炎病例。几乎所有患者都有先前的瓣膜置换手术或免疫功能低下。有 3 例合并脑膜炎。3 例患者进行了手术。总体死亡率为 44.4%。

结论

隐球菌性心内膜炎罕见,死亡率高。几乎所有患者都有基础疾病。诊断需要重复血液培养和超声心动图检查,有时还需要腰椎穿刺排除脑膜炎。

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