A Case of Neurofollicular Hamartoma.
- Author:
Jin Gu KIM
1
;
Hwa Mi KIM
;
Chi Yeon KIM
Author Information
1. Department of Dermatology and Institute of Health Science, School of Medicine, Gyeongsang National University, Jinju, Korea. dr_chiny@hotmail.com
- Publication Type:Case Report
- Keywords:
Neurofollicular hamartoma;
Pilosebaceous hyperplasia;
S-100
- MeSH:
Adult;
Angiofibroma;
Carcinoma, Basal Cell;
Diagnosis, Differential;
Hamartoma;
Humans;
Light;
Nasolabial Fold;
Nevus, Intradermal;
Nose
- From:Korean Journal of Dermatology
2012;50(1):39-42
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Neurofollicular hamartoma is an unusual, previously described neoplasm characterized by a stroma composed of proliferation of spindle cells and hyperplastic pilosebaceous units. The stroma has light microscopic and immunohistochemical features consistent with neuroid differentiation showing positive S-100 antigen. Lesions are almost invariably located on the face with strong predilection for the nose or nasolabial fold. A 35-year-old man presented with a solitary, skin-colored, dome-shaped papule that had been present on his right temple area for a few years. Clinical differential diagnosis included basal cell carcinoma, angiofibroma and intradermal nevus. Clinically, the lesion presents as a small, skin-colored, dome-shaped firm papule, 3 to 7 mm in diameter. Although clinical aspects of the lesion are not diagnostic, the histological features are very typical. Herein, we report a rare case of neurofollicular hamartoma on the right temple area.
