Epidermolysis bullosa nevus in a patient with recessive dystrophic epidermolysis bullosa: A case report Journal Article


Authors: Fening, K.; Theos, A.; Andea, A.; Vincent, B.; Busam, K.; McKay, K.
Article Title: Epidermolysis bullosa nevus in a patient with recessive dystrophic epidermolysis bullosa: A case report
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. © 2013 Lippincott Williams & Wilkins.
Keywords: immunohistochemistry; child; human tissue; preschool child; unclassified drug; gene mutation; human cell; case report; follow up; ki 67 antigen; melanin; skin pigmentation; dermoepidermal junction; melanocyte; protein; punch biopsy; tissue section; fluorescence in situ hybridization; scar formation; melan a; microphthalmia associated transcription factor; epidermolysis bullosa; epidermolysis bullosa dystrophica; copy number variation; erosion; melanosome; human; female; priority journal; article; epidermolysis bullosa nevus; pseudomelanoma; melanocytic neoplasm; col7a1 protein
Journal Title: American Journal of Dermatopathology
Volume: 36
Issue: 12
ISSN: 0193-1091
Publisher: Lippincott Williams & Wilkins  
Date Published: 2014-12-01
Start Page: e194
End Page: e197
Language: English
DOI: 10.1097/DAD.0000000000000059
PROVIDER: scopus
PUBMED: 25051104
DOI/URL:
Notes: Export Date: 2 April 2015 -- Source: Scopus
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  1. Klaus J Busam
    688 Busam