Bartralot R, Garcia-Patos V, Hueto J, Huguet P, Raspall G, Castells A
Department of Dermatology, Hospital General Universitari Vall d'Hebron, Barcelona, Spain.
Br J Dermatol. 1996 Apr;134(4):744-8.
Angiolymphoid hyperplasia with eosinophilia (ALHE) is an uncommon disorder of unknown aetiology. Clinically, it is characterized by cutaneous papules or nodules on the head and neck, and extracutaneous involvement is rare. We report a 30-year-old woman who had an asymptomatic submucosal nodule on the upper lip, which histopathologically showed features of ALHE, and review the previously described 15 cases of oral ALHE.
嗜酸性粒细胞增多性血管淋巴样增生(ALHE)是一种病因不明的罕见疾病。临床上,其特征为头颈部出现皮肤丘疹或结节,皮肤外受累情况罕见。我们报告一名30岁女性,其上唇有一个无症状的黏膜下结节,组织病理学显示为ALHE特征,并回顾了先前报道的15例口腔ALHE病例。