Juvenile temporal arteritis with hypereosinophilic syndrome masquerading as an epidermal inclusion cyst of the scalp

IF 0.1 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Maheshri Deshpande, Geet Bhuyan
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引用次数: 0

Abstract

A 34-year-old man came to the outpatient department with subcutaneous nodules in the temporal area. He did not complain of any other symptoms. Computed tomography scan revealed a nodule of 40.5 HU in the temporal region of the scalp. A possibility of an epidermal inclusion cyst was given. The lesion was excised and the biopsy revealed vasculitis with eosinophilia without giant cell formation. A final diagnosis of juvenile temporal arteritis with hypereosinophilic syndrome was given based on the clinical, radiological, and histopathological findings.
青少年颞动脉炎伴嗜酸性粒细胞增多综合征,伪装成头皮表皮包皮囊肿
一个34岁的男人来到门诊部皮下结节在颞区。他没有抱怨任何其他症状。计算机断层扫描显示头皮颞区有一个40.5 HU的结节。有可能是表皮包涵性囊肿。病变被切除,活检显示血管炎伴嗜酸性粒细胞增多,无巨细胞形成。根据临床、放射学和组织病理学结果,最终诊断为青少年颞动脉炎伴嗜酸性粒细胞增多综合征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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42
审稿时长
12 weeks
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