Tchernev Georgi, Taneva Teodora, Ananiev Julian, Cardoso José Carlos, Gulubova Maya, Velev Valentin, Karashmalakov Anatoli, Zisova Liliya, Geilen Christoph C
Polyclinic for Dermatology and Venerology, Saint Kliment Ohridski University, Medical faculty, University Hospital Lozenetz, Koziak Str. 1, 1407 Sofia, Bulgaria.
Wien Med Wochenschr. 2012 Oct;162(19-20):448-51. doi: 10.1007/s10354-012-0138-4. Epub 2012 Sep 7.
Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare benign vasoproliferative lesion. Although it is a benign disease, lesions are often persistent and difficult to eradicate. ALHE typically presents clinically as papules or nodules, tan, brown, pink or dull red in colour, located predominantly in the head and neck region, especially around the ears and on the forehead and scalp.All races can be affected and no gender predominance exists. The disease also has nonspecific clinical features, hence it requires in most of the cases biopsy for accurate diagnosis. We present an uncommon clinical presentation of the disease, mimicking clinically a subcutaneous lipomatous mass, which has been treated successfully with surgical excision.
嗜酸性粒细胞增多性血管淋巴样增生（ALHE）是一种罕见的良性血管增生性病变。虽然它是一种良性疾病，但病变往往持续存在且难以根除。ALHE在临床上通常表现为丘疹或结节，颜色为棕褐色、粉红色或暗红色，主要位于头颈部区域，尤其是耳部周围以及前额和头皮。所有种族均可受累，且无性别差异。该疾病还具有非特异性临床特征，因此在大多数情况下需要进行活检以准确诊断。我们报告了该疾病一种不常见的临床表现，临床上酷似皮下脂肪瘤块，经手术切除已成功治愈。
