Gencoglan Gulsum, Karaca Semsettin, Ertekin Banu
Dermatology Department, Afyon Kocatepe University Medical School, Afyon, Turkey.
Dermatology. 2007;215(3):233-5. doi: 10.1159/000106581.
Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disorder characterized by vascular proliferation, eosinophilia in peripheral blood samples and lymphocytosis. The etiology is unknown; this rare condition is generally seen in women. It often presents as multiple, grouped red nodules in the periauricular region, scalp line and neck. Numerous therapeutic approaches have been tried for ALHE including destructive techniques such as electrodesiccation, cryotherapy, surgical excision, radiotherapy or laser (argon, CO(2), pulse dye). We present an ALHE case that was treated successfully by using topical imiquimod cream.
伴有嗜酸性粒细胞增多的血管淋巴样增生(ALHE)是一种罕见疾病,其特征为血管增生、外周血样本中嗜酸性粒细胞增多以及淋巴细胞增多。病因不明;这种罕见病症通常见于女性。它常表现为耳周区域、头皮线和颈部的多个、成组的红色结节。针对ALHE已经尝试了多种治疗方法,包括如电干燥、冷冻疗法、手术切除、放射治疗或激光(氩气、二氧化碳、脉冲染料)等破坏性技术。我们报告一例通过使用咪喹莫特乳膏成功治疗的ALHE病例。