Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases
Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases
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DOI：
10.1016/j.ad.2013.03.009
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发表时间：
2014-03-01
影响因子：
3.2
通讯作者：
Ferrandiz, C.
中科院分区：
文献类型：
--
作者：
Guinovart, R. M.;Bassas-Vila, J.;Ferrandiz, C.
血管淋巴样增生伴嗜酸性粒细胞增多症是一种罕见的疾病，其特征是通常位于头皮和面部的单个或多个血管瘤样病变。我们对9例ALHE进行回顾性分析。病变主要表现为多发性成组丘疹，或在某些情况下，皮下结节，主要位于头皮，特别是耳周。我们还观察到非典型部位的病变，如头皮以外的头部区域、肩部、颈部和前臂。在这些部位，病变具有非典型的临床表现，使得诊断困难;对于具有血管外观和浅表溃疡或结痂的单个、边界界定的病变的患者，应记住这一点。手术是我们系列中最常见的治疗方法，即使ALHE被认为是良性疾病，复发也很常见。(C)2012 Elsevier Espana，S.L. AEDV。All rights reserved.
Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, welt-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. (C) 2012 Elsevier Espana, S.L. and AEDV. All rights reserved.