Porokeratotic eccrine duct and hair follicle nevus (PEHFN) associated with keratitis-ichthyosis-deafness (KID) syndrome

Pediatr Dermatol. 2010 Sep-Oct;27(5):514-7. doi: 10.1111/j.1525-1470.2010.01272.x.

Abstract

Porokeratotic eccrine ostial and dermal duct nevus is a rare hamartomatous malformation, histologically characterized by cornoid lamellae overlying dilated eccrine ostia. The nevus most commonly presents in the form of multiple filiform keratotic spines in a linear arrangement, usually on the distal extremities. Porokeratotic eccrine and hair follicle nevus is thought to be a variant of porokeratotic eccrine ostial and dermal duct nevus that additionally involves hair follicle infundibula. We report a case of widespread Porokeratotic eccrine and hair follicle nevus that developed in a 15-year-old woman with keratitis-ichthyosis-deafness syndrome.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Biopsy
  • Deafness / pathology
  • Facial Neoplasms / pathology
  • Female
  • Hair Follicle / pathology*
  • Humans
  • Ichthyosis / pathology
  • Keratitis / pathology
  • Nevus, Intradermal / pathology*
  • Porokeratosis / pathology*
  • Sweat Gland Neoplasms / pathology*

Supplementary concepts

  • Keratitis, Ichthyosis, and Deafness (KID) Syndrome