The granuloma faciale is a rare and benign skin disease of unknown etiology,
characterized by chronic leukocitoclastic vasculitis. It is characterized by skin
lesions predominantly facial whose course is chronic and slowly progressive. The
diagnosis is based on clinical features, histopathology and, more recently, in
dermoscopy. We describe the case of a male patient, 40 years old, with a sarcoid
lesion on the malar site, whose histopathological examination revealed a mixed
inflammatory infiltrate with presence of Grenz zone. Dermoscopy revealed a pink
background with white striations. The definitive diagnosis is made by histopathologic
evaluation, and dermatoscopy can be helpful. It is known to be resistant to therapy,
oral medications, intralesional and surgical procedures are options.