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造血干细胞移植后肉芽肿性阿米巴脑炎

Granulomatous amebic encephalitis following hematopoietic stem cell transplantation.

作者信息

Doan Ninh, Rozansky Gregory, Nguyen Ha Son, Gelsomino Michael, Shabani Saman, Mueller Wade, Johnson Vijay

机构信息

Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

Department of Neurology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

出版信息

Surg Neurol Int. 2015 Oct 7;6(Suppl 18):S459-62. doi: 10.4103/2152-7806.166788. eCollection 2015.

Abstract

BACKGROUND

Granulomatous amebic encephalitis (GAE) is rare, but often fatal. The infection has been documented predominantly among the immunocompromised population or among those with chronic disease. To date, however, there have only been eight cases regarding the infection following hematopoietic stem cell transplantation (HSCT).

CASE DESCRIPTION

A 62-year-old female with a history of relapsed diffuse large B-cell lymphoma, recently underwent peripheral blood autologous stem cell transplant after BEAM conditioning (day 0). On day +15, she began to exhibit worsening fatigue, generalized weakness, and fever. Symptoms progressed to nausea, emesis, somnolence, confusion, and frontal headaches over the next few days. Imaging demonstrated multifocal ill-defined vasogenic edema with patchy enhancement. The patient was started on broad antibiotics, antifungals, and seizure prophylaxis. Evaluation for bacterial, fungal, mycobacterial, and viral etiologies was fruitless. Her mental status progressively deteriorated. On day +22, she exhibited severe lethargy and went into pulseless electrical activity arrest, requiring chest compressions. The episode lasted <2 min and her pulse was restored. She was taken to the operating room for a brain biopsy. Postoperatively, her right pupil began to dilate compared to the left; she demonstrated extensor posturing in her upper extremities and withdrawal in her lower extremities. Repeat computed tomography demonstrated progressive edema. Given poor prognosis and poor neurological examination, the family opted for withdrawal of care. Final pathology was consistent with Acanthamoeba GAE.

CONCLUSION

The authors report the third case of GAE after autologous stem cell transplant, and the ninth case overall after HSCT. This case is unusual due to its rapid clinical presentation after HSCT compared to prior literature. The case highlights the need for high suspicion of Acanthamoeba infection in this patient population.

摘要

背景

肉芽肿性阿米巴脑炎(GAE)较为罕见,但往往致命。该感染主要见于免疫功能低下人群或患有慢性疾病的人群。然而,迄今为止,造血干细胞移植(HSCT)后发生该感染的病例仅有8例。

病例描述

一名62岁女性,有复发性弥漫性大B细胞淋巴瘤病史,近期在接受BEAM预处理(第0天)后进行了外周血自体干细胞移植。在第+15天,她开始出现疲劳加重、全身无力和发热症状。在接下来的几天里,症状进展为恶心、呕吐、嗜睡、意识模糊和前额头痛。影像学检查显示多灶性边界不清的血管源性水肿伴斑片状强化。患者开始接受广谱抗生素、抗真菌药物治疗及癫痫预防。对细菌、真菌、分枝杆菌和病毒病因的评估均无结果。她的精神状态逐渐恶化。在第+22天,她出现严重嗜睡并进入无脉电活动骤停状态,需要进行胸外按压。该发作持续时间<2分钟,脉搏恢复。她被送往手术室进行脑活检。术后,她的右瞳孔开始比左瞳孔扩大;她的上肢出现伸直姿势,下肢出现回缩。重复计算机断层扫描显示水肿进展。鉴于预后不良和神经检查结果不佳,家属选择放弃治疗。最终病理结果与棘阿米巴GAE相符。

结论

作者报告了自体干细胞移植后GAE第三例,也是HSCT后总体第九例。与既往文献相比,该病例因HSCT后临床表现迅速而不同寻常。该病例强调了对该患者群体高度怀疑棘阿米巴感染的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e4/4604647/714d30a78c66/SNI-6-459-g001.jpg

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