Epidermolysis bullosa nevus in a patient with recessive dystrophic epidermolysis bullosa: a case report. Academic Article uri icon

Overview

MeSH

  • Axilla
  • Child
  • Female
  • Humans

MeSH Major

  • Epidermolysis Bullosa Dystrophica
  • Nevus, Pigmented
  • Skin Neoplasms

abstract

  • We present a case of a 6-year-old girl with recessive dystrophic epidermolysis bullosa (EB) who presented with a large pigmented lesion clinically concerning for melanoma. After histological examination and fluorescent in situ hybridization analysis, diagnosis of EB nevus was performed. EB nevi are benign melanocytic neoplasms with histological findings similar to recurrent nevi occurring in all types of EB. They often mimic melanoma clinically, dermatoscopically, and histopathologically. The ability to recognize an EB nevus is essential for appropriate management of the patient. Unnecessary surgical excision in patients with already high-risk EB should be avoided. Close monitoring of these lesions is recommended because no cases of transformation to melanoma have been described.

publication date

  • December 2014

has subject area

  • Axilla
  • Child
  • Epidermolysis Bullosa Dystrophica
  • Female
  • Humans
  • Nevus, Pigmented
  • Skin Neoplasms

Research

keywords

  • Case Reports
  • Journal Article

Identity

Language

  • eng

Digital Object Identifier (DOI)

  • 10.1097/DAD.0000000000000059

PubMed ID

  • 25051104

Additional Document Info

start page

  • e194

end page

  • e197

volume

  • 36

number

  • 12