巨细胞动脉炎患者的皮肤诺卡菌病表现为额部肿块。

Clujul medical (1957) Pub Date : 2017-01-01 Epub Date: 2017-04-25 DOI:10.15386/cjmed-726
Violeta Tincuta Briciu, Mirela Flonta, Mihaela Lupse, Laura Damian
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引用次数: 1

摘要

我们报告一例皮下脓肿由于诺卡菌属模拟自发性血肿或动脉瘤的颞动脉分支,在巨细胞动脉炎患者接受甲基强的松龙和硫唑嘌呤治疗。超声检查、切口引流及培养有助于诊断。这个病例强调了在免疫抑制患者中考虑罕见病原体的重要性,除了更常见的疾病并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cutaneous nocardiosis manifesting as a frontal mass in a patient with giant cell arteritis.

Cutaneous nocardiosis manifesting as a frontal mass in a patient with giant cell arteritis.

Cutaneous nocardiosis manifesting as a frontal mass in a patient with giant cell arteritis.

Cutaneous nocardiosis manifesting as a frontal mass in a patient with giant cell arteritis.

We report the case of a subcutaneous abscess due to Nocardia spp. mimicking a spontaneous hematoma or an aneurysm of the temporal artery branch, in a giant cell arteritis patient treated with methylprednisolone and azathioprine. Ultrasonography, incision and drainage with cultures helped in the diagnosis. This case highlights the importance of considering rare pathogens in immunosuppressed patients, besides the more frequent disease complications.

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