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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.

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。

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