Dear Editor, Folliculosebaceous cystic hamartoma (FSCH) is a rare skin lesion comprised of follicular, sebaceous and mesenchymal elements. FSCH mostly involves the head and neck area but some cases involving the upper back, forearm and ear have been reported. However, FSCH located on the nipple is quite rare. Herein, we describe a case of FSCH on the nipple of a 32-year-old woman.A 32-year-old woman visited our clinic to evaluate a single pedunculated soft nodule on the nipple of her right breast. The nodule had been there for 5 years. It was asymptomatic and very slowly growing. The surrounding areola and underlying mammary ducts and breast tissue were unremarkable. There was no history of nipple discharge or bleeding. Her left breast was normal.On physical examination, the lesion was a 0.5 cm · 0.4 cm · 0.3 cm, light brown, soft tumor with a projecting and polypoid configuration, located on the superolateral aspect of the right nipple. There was no evidence of punctum or sinus opening and involvement of ductal orifice was not noticed (Fig. 1). Initial clinical diagnosis was fibroma of the nipple and accessory nipple, and an excisional biopsy was performed.The tumor was totally excised by a 6-mm punch. Histopathological examination revealed mild epidermal proliferation and hyperplasia. Within the dermis, there were multiple hyperplastic sebaceous glands forming nodules around a large, cysticallydilated, follicular infundibular structure lined with stratified squamous epithelium and filled with keratin material. Sebaceous lobules were attached to the cystic structure through sebaceous ducts. The surrounding stroma consisted of concentric, fibrillary bundles of collagen with numerous dilated capillaries and venules. The perifollicular part of the stroma contained large amounts of mucin. There was cleft formation between the perifollicular stroma and the adjacent dermis (Fig. 2). The final diagnosis was folliculosebaceous cystic hamartoma and the lesion has not recurred after total excision.Folliculosebaceous cystic hamartoma was first described in 1991 by Kimura et al.1 and was con-