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表现为巨大腋动脉瘤的嗜酸性粒细胞增多性血管淋巴样增生。

Angiolymphoid hyperplasia with eosinophilia presenting as a giant axillary artery aneurysm.

作者信息

Bhat Seetharama P S, Moorthy Nagaraja, Ramalingam Rangaraj, Jayapal Mithravrinda, Nanjappa Manjunath Cholenahalli

机构信息

Department of Cardiothoracic and Vascular Surgery, Sri Jayadeva Institute of Cardiology, Bangalore, India.

出版信息

Vascular. 2010 Jan-Feb;18(1):49-52. doi: 10.2310/6670.2009.00041.

Abstract

Angiolymphoid hyperplasia with eosinophilia (ALHE) is an unusual vascular tumor most frequently located in the superficial head and neck. Noncutaneous localization of this pathology in large arteries presenting as a pulsatile mass is extremely rare. We describe an adult male with a giant left axillary artery tumor secondary to ALHE. ALHE should be considered in the differential diagnosis of localized peripheral arterial masses, especially in young patients.

摘要

嗜酸性粒细胞增多性血管淋巴样增生(ALHE)是一种罕见的血管肿瘤,最常发生于头颈部浅表部位。这种病变在大动脉中非皮肤部位表现为搏动性肿块极为罕见。我们描述了一名成年男性,其左腋动脉巨大肿瘤继发于ALHE。在鉴别诊断局限性外周动脉肿块时应考虑ALHE,尤其是在年轻患者中。

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