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棘阿米巴引起的暴发性致死性脑炎在肾移植受者中的病例报告及文献复习

Fulminant and fatal encephalitis caused by Acanthamoeba in a kidney transplant recipient: case report and literature review.

作者信息

Satlin M J, Graham J K, Visvesvara G S, Mena H, Marks K M, Saal S D, Soave R

机构信息

Division of Infectious Diseases, Department of Medicine, Weill Cornell Medical College, New York, New York, USA; Transplantation-Oncology Infectious Diseases Program, Department of Medicine, Weill Cornell Medical College, New York, New York, USA.

出版信息

Transpl Infect Dis. 2013 Dec;15(6):619-26. doi: 10.1111/tid.12131. Epub 2013 Sep 9.

Abstract

Acanthamoeba is the most common cause of granulomatous amebic encephalitis, a typically fatal condition that is classically described as indolent and slowly progressive. We report a case of Acanthamoeba encephalitis in a kidney transplant recipient that progressed to death within 3 days of symptom onset and was diagnosed at autopsy. We also review clinical characteristics, treatments, and outcomes of all published cases of Acanthamoeba encephalitis in solid organ transplant (SOT) recipients. Ten cases were identified, and the infection was fatal in 9 of these cases. In 6 patients, Acanthamoeba presented in a fulminant manner and death occurred within 2 weeks after the onset of neurologic symptoms. These acute presentations are likely related to immunodeficiencies associated with solid organ transplantation that result in an inability to control Acanthamoeba proliferation. Skin lesions may predate neurologic involvement and provide an opportunity for early diagnosis and treatment. Acanthamoeba is an under-recognized cause of encephalitis in SOT recipients and often presents in a fulminant manner in this population. Increased awareness of this disease and its clinical manifestations is essential to attain an early diagnosis and provide the best chance of cure.

摘要

棘阿米巴是肉芽肿性阿米巴脑炎最常见的病因,这是一种典型的致命疾病,通常被描述为隐匿性且进展缓慢。我们报告了一例肾移植受者的棘阿米巴脑炎病例,该病例在症状出现后3天内进展至死亡,并在尸检时确诊。我们还回顾了实体器官移植(SOT)受者中所有已发表的棘阿米巴脑炎病例的临床特征、治疗方法及转归。共确定了10例病例,其中9例感染是致命的。在6例患者中,棘阿米巴呈暴发性表现,神经症状出现后2周内死亡。这些急性表现可能与实体器官移植相关的免疫缺陷有关,导致无法控制棘阿米巴的增殖。皮肤病变可能先于神经受累出现,为早期诊断和治疗提供了机会。棘阿米巴是SOT受者中一种未被充分认识的脑炎病因,在该人群中常呈暴发性表现。提高对这种疾病及其临床表现的认识对于早期诊断和提供最佳治愈机会至关重要。

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