Cutaneous Acanthamoebiasis with CNS Involvement Post- Transplantation: Implication for Differential Diagnosis of Skin Lesions in Immunocompromised Patients

Andrea A. D’Auria, J. Lin, P. Geiseler, Y. Qvarnstrom, Rebecca Bandea, S. Roy, R. Sriram, C. Paddock, S. Zaki, Gene H. Kim, G. Visvesvara
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引用次数: 21

Abstract

We report a 62-year-old male who presented status post lung transplantation with subcutaneous nodules. One week later, he showed signs of altered mental status; brain imaging demonstrated mass effect in the cerebellum and meningoencephalitis. In spite of treatment with a broad range of antimicrobials, he died. A punch biopsy of the skin lesions showed a superficial and deep mixed inflammatory infiltrate admixed with large mononuclear cells. A diagnosis of cutaneous amoebiasis was made and the amoebae were identified as Acanthamoeba spp. based on immunofluorescent stains and PCR assays. Cutaneous Acanthamoebiasis is a rare infection in immunocompro- mised patients, particularly organ recipients. It is important that this entity is included in the differential diagnosis of immunocompromised patients who have cutaneous infections that are not responding to antibiotics. An early diagnosis is crucial since cutaneous Acanthamoebiasis can disseminate to the central nervous system and cause granulomatous amoebic encephalitis (GAE), which is usually fatal.
移植后累及中枢神经系统的皮肤棘阿米巴病:免疫功能低下患者皮肤病变鉴别诊断的意义
我们报告一个62岁的男性谁提出状态后肺移植皮下结节。一周后,他出现了精神状态改变的迹象;脑成像显示小脑肿块效应和脑膜脑炎。尽管接受了广泛的抗菌素治疗,他还是死了。皮肤损伤的穿刺活检显示浅、深混合性炎症浸润,并伴有大的单个核细胞。经免疫荧光染色和PCR检测,诊断为皮肤阿米巴病,鉴定为棘阿米巴属。皮肤棘阿米巴病是一种罕见的感染免疫功能低下的病人,特别是器官接受者。重要的是,在对抗生素无反应的皮肤感染免疫功能低下患者的鉴别诊断中应包括这一实体。早期诊断是至关重要的,因为皮肤棘阿米巴病可以传播到中枢神经系统,并引起肉芽肿性阿米巴脑炎(GAE),这通常是致命的。
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