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Balamuthia mandrillaris therapeutic mud bath in Jamaica.牙买加的曼氏巴通体治疗泥浴。
Epidemiol Infect. 2015 Jul;143(10):2245-8. doi: 10.1017/S0950268814002842. Epub 2014 Oct 22.
2
An autopsy case of Balamuthia mandrillaris amoebic encephalitis, a rare emerging infectious disease, with a brief review of the cases reported in Japan.一例罕见的新发传染病——曼氏巴通体阿米巴脑炎尸检病例,并简要回顾日本报告的病例
Neuropathology. 2015 Feb;35(1):64-9. doi: 10.1111/neup.12151. Epub 2014 Sep 3.
3
Isolation and molecular characterization of Acanthamoeba and Balamuthia mandrillaris from combination shower units in Costa Rica.从哥斯达黎加的组合淋浴设备中分离棘阿米巴和曼氏巴贝斯虫并进行分子特征分析。
Parasitol Res. 2014 Nov;113(11):4117-22. doi: 10.1007/s00436-014-4083-6. Epub 2014 Aug 19.
4
Transmission of Balamuthia mandrillaris through solid organ transplantation: utility of organ recipient serology to guide clinical management.曼氏巴尔通体通过实体器官移植传播:器官受者血清学在指导临床管理中的应用。
Am J Transplant. 2014 Jun;14(6):1417-24. doi: 10.1111/ajt.12726. Epub 2014 May 19.
5
The isolation of Balamuthia mandrillaris from environmental sources from Peru.从秘鲁环境样本中分离曼氏巴尔通体。
Parasitol Res. 2014 Jul;113(7):2509-13. doi: 10.1007/s00436-014-3900-2. Epub 2014 Apr 30.
6
Successful treatment of granulomatous amoebic encephalitis with combination antimicrobial therapy.联合抗菌疗法成功治疗肉芽肿性阿米巴脑炎。
Intern Med. 2013;52(17):1977-81. doi: 10.2169/internalmedicine.52.0299.
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Cutaneous amebiasis: 50 years of experience.皮肤阿米巴病:50年的经验
Cutis. 2012 Dec;90(6):310-4.
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Balamuthia mandrillaris amoebic encephalitis: an emerging parasitic infection.曼氏迭宫绦虫蚴性脑炎:一种新出现的寄生虫感染。
Curr Infect Dis Rep. 2012 Aug;14(4):391-6. doi: 10.1007/s11908-012-0266-4.
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Granulomatous amoebic encephalitis caused by Balamuthia mandrillaris in an immunocompetent girl.曼氏迭宫绦虫感染致免疫功能正常女童肉芽肿性阿米巴脑炎
World Neurosurg. 2012 Dec;78(6):715.e7-12. doi: 10.1016/j.wneu.2011.10.040. Epub 2011 Nov 1.
10
Successful treatment of Balamuthia mandrillaris amoebic infection with extensive neurological and cutaneous involvement.成功治疗广泛累及神经和皮肤的狨猴阿米巴原虫感染。
Clin Infect Dis. 2010 Jul 15;51(2):e7-11. doi: 10.1086/653609.

面部中央巴拉姆希阿米巴病:一例罕见皮肤阿米巴感染的病例报告。

Centrofacial Balamuthiasis: case report of a rare cutaneous amebic infection.

作者信息

Chang Oliver H, Liu Fan, Knopp Eleanor, Muehlenbachs Atis, Cope Jennifer R, Ali Ibne, Thompson Robert, George Evan

机构信息

Department of Anatomic Pathology, University of Washington, Seattle, WA, USA.

Division of Dermatology, Department of Medicine, University of Washington, Seattle, WA, USA.

出版信息

J Cutan Pathol. 2016 Oct;43(10):892-7. doi: 10.1111/cup.12748. Epub 2016 Jul 12.

DOI:10.1111/cup.12748
PMID:27251900
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5033676/
Abstract

Free-living amebae are ubiquitous in our environment, but rarely cause cutaneous infection. Balamuthia mandrillaris has a predilection for infecting skin of the central face. Infection may be restricted to the skin or associated with life-threatening central nervous system (CNS) involvement. We report a case of a 91-year-old woman, who presented with a non-healing red plaque over her right cheek. Several punch biopsies exhibited non-specific granulomatous inflammation without demonstrable fungi or mycobacteria in histochemical stains. She was treated empirically for granulomatous rosacea, but the lesion continued to progress. A larger incisional biopsy was performed in which amebae were observed in hematoxylin-eosin stained sections. These were retrospectively apparent in the prior punch biopsy specimens. Immunohistochemistry and polymerase chain reaction studies identified the organisms as Balamuthia mandrillaris. Cutaneous infection by B. mandrillaris is a rare condition that is sometimes complicated by life-threatening CNS involvement and which often evades timely diagnosis due to its rarity and nonspecific clinical manifestations. Moreover, these amebae are easily overlooked in histopathologic sections because of their small number and their resemblance to histiocytes. Dermatopathologists should be familiar with the histopathologic appearance of these organisms and include balamuthiasis and other amebic infections in the differential diagnosis of granulomatous dermatitis.

摘要

自由生活的阿米巴在我们的环境中无处不在,但很少引起皮肤感染。曼氏巴通体(Balamuthia mandrillaris)倾向于感染面部中央的皮肤。感染可能局限于皮肤,也可能伴有危及生命的中枢神经系统(CNS)受累。我们报告一例91岁女性病例,她右侧脸颊出现一个不愈合的红色斑块。多次打孔活检显示非特异性肉芽肿性炎症,组织化学染色未发现明显的真菌或分枝杆菌。她接受了肉芽肿性酒渣鼻的经验性治疗,但病变仍持续进展。进行了一次更大的切开活检,在苏木精-伊红染色切片中观察到阿米巴。这些在之前的打孔活检标本中回顾性地明显可见。免疫组织化学和聚合酶链反应研究确定这些生物体为曼氏巴通体。曼氏巴通体引起的皮肤感染是一种罕见疾病,有时会因危及生命的中枢神经系统受累而复杂化,并且由于其罕见性和非特异性临床表现,常常难以得到及时诊断。此外,这些阿米巴在组织病理学切片中很容易被忽视,因为它们数量少且与组织细胞相似。皮肤病理学家应熟悉这些生物体的组织病理学表现,并在肉芽肿性皮炎的鉴别诊断中考虑巴通体病和其他阿米巴感染。