Abstract
We performed the surgical treatment of oral cavity to a 53-year-old male patient which have been recessive dystrophic epidermolysis bullosa hereditaria (RDEB), and reports for successful treatment on this paper. He complained of severe trismus and difficulty in mastication, which were caused by RDEB, before the surgical treatment. Under the local anesthesia, the vestibular extension was performed in consideration of strong hope of the patient. We worried that the scartissue was formed again, therefore the dentures were made at the early stage of wound healing. Ten months are passing from the wearing of the dentures now, and there are no blisters at the oral mucosa to touch the denture. The patient feels pleasure in remarkable increasing of the kind of food which can be taken.
