%0 Journal Article %T Clinical and histological findings of a typical case of angiolymphoid hyperplasia without eosinophilia: a rare and difficult-to-treat disease %V 10 %N 3 %P 275-277 %U http://www.odermatol.com/issue-in-html/2019-3-13-angiolymphoid/ %X Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare vascular condition characterized by cutaneous papules, plaques or nodules, predominantly located on the head and neck. The main differential diagnosis of ALHE is Kimura’s disease. The treatment is a challenge and the gold standard treatment is surgical excision, as relapse is commonly observed. We report a case of a 57-year-old female with ALHE with an unusual clinical improvement at 2-month follow-up after topical corticosteroid without recurrence 12 months after treatment. Due to its rarity, ALHE can be misdiagnosed. In this case, the characteristic lesions in typical location supported our first clinical diagnose, which was confirmed by histological studies. The clinical improvement after topical steroids without recurrence after long period follow-up caught our attention. %G en %J Our Dermatology Online %A Hernandez, Ivonne Dannesy Rodriguez %D 2019-07-02