Chacon Anna, Mercer Jessica
Department of Dermatology and Cutaneous Surgery, Orlando Regional Medical Center, University of Central Florida College of Medicine, Orlando, FL USA -
G Ital Dermatol Venereol. 2016 Aug;151(4):436-40. Epub 2014 Jul 11.
Angiolymphoid hyperplasia with eosinophilia (ALHE) is an uncommon, benign condition characterized by multiple benign angiomatous nodules or plaques. Cutaneous lesions can be painful, pruritic, pulsatile, or potentially disfiguring resulting in significant morbidity. ALHE is a pathologic diagnosis featuring proliferations of capillary-sized vessels with epithelioid endothelial cells surrounded by larger, thick-walled vessels and accompanying eosinophils and lymphocytes. Surgery is generally required, however the skin lesions often recur after excision. ALHE is notoriously difficult to treat and many physicians would prefer a non-invasive treatment of choice. We report a case of ALHE that was successfully treated with the novel use of topical tacrolimus in a split-face trial with topical timolol solution.
嗜酸性粒细胞增多性血管淋巴样增生(ALHE)是一种罕见的良性疾病,其特征为多个良性血管瘤性结节或斑块。皮肤病变可能会疼痛、瘙痒、有搏动性,或者有潜在毁容性,从而导致严重的发病率。ALHE是一种病理诊断,其特征为毛细血管大小的血管增生,伴有上皮样内皮细胞,周围是较大的厚壁血管,并伴有嗜酸性粒细胞和淋巴细胞。通常需要手术治疗,然而皮肤病变在切除后常复发。ALHE notoriously难以治疗,许多医生更倾向于选择非侵入性治疗方法。我们报告一例ALHE病例,该病例在一项使用局部噻吗洛尔溶液的半脸试验中,通过局部使用他克莫司的新方法成功得到治疗。