Angiolymphoid hyperplasia with eosinophilia: A report of a rare entity in an elderly male

Abstract

Angiolymphoid hyperplasia with eosinophilia (ALHE) is an uncommon benign proliferation of blood vessels of uncertain etiology. It primarily affects the head-and-neck region. Histologically, it is characterized by the prominent proliferation of plump endothelial cells, and accompanying eosinophilic and lymphocytic infiltration. Herein, we report the case of ALHE in a 65-year-old male.

Keywords

• angiolymphoid hyperplasia with eosinophilia
• epithelioid hemangioma
• histiocytoid hemangioma