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

Overview

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 1, 2014

Research

keywords

  • Epidermolysis Bullosa Dystrophica
  • Nevus, Pigmented
  • Skin Neoplasms

Identity

Scopus Document Identifier

  • 84924030632

Digital Object Identifier (DOI)

  • 10.1097/DAD.0000000000000059

PubMed ID

  • 25051104

Additional Document Info

volume

  • 36

issue

  • 12