The interaction of inflammatory cells in granuloma faciale.

Granuloma faciale (GF) is a rare chronic inflammatory skin disease characterized by single or multiple reddish-brown cutaneous plaques or nodules. Although this condition is benign, its clinical course is extremely chronic with poor response to therapy. The typical histopathological features of GF include vasculitis with mixed cellular infiltration; however, its etiopathogenesis remains unknown.

Traumatic neuroma of the lower lip with intraepithelial nerve fibers.

A 42-year-old man had noticed a small tender papule on his lower lip, and the papule clinically became unnoticeable after cryosurgery. He visited our clinic because the lesion recurred up to the original size after 9 months. On examination, a linear scar and a papule, 4 mm in diameter, were observed on the mucosal lower lip.

COL7A1 mutation G2037E causes epidermal retention of type VII collagen.

COL7A1 glycine substitution (GS) mutations result in dominant and recessive dystrophic epidermolysis bullosa (DDEB and RDEB). Here, we report a DDEB family in which retention of type VII collagen by epidermal keratinocytes was observed for a female proband. Mutational analysis detected a GS mutation, G2037E, in the proband and her affected father.