RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Marciniak, Bruno A1 Dalens, Bernard J. SR Print(0) ID 58083626 T1 Porokeratosis of Mibelli T2 Syndromes: Rapid Recognition and Perioperative Implications YR 2006 FD 2006 PB The McGraw-Hill Companies PP New York, NY SN 9780071354554 LK accessanesthesiology.mhmedical.com/content.aspx?aid=58083626 RD 2024/03/28 AB Congenital or acquired genodermatosis disorder of keratinization. Clinically, presents one or more atrophic patches surrounded by a distinctive ridge-like border called the cornoid lamella. There are five variants and the disseminated superficial actinic porokeratosis is relatively common.