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Verruciform xanthoma in recessive dystrophic epidermolysis bullosa and keratitis-ichthyosis-deafness syndrome: Report of two cases and a review of the literature.

Publication ,  Journal Article
Evan-Browning, E; Rork, J; O'Donnell, P; Elaba, Z; Deng, A; Wiss, K
Published in: Pediatr Dermatol
January 2020

Verruciform xanthoma is a benign, wart-like lesion that can clinically mimic squamous cell carcinoma. We describe two teenage patients with severe genodermatoses, recessive dystrophic epidermolysis bullosa (RDEB), and keratitis-ichthyosis-deafness (KID) syndrome, respectively, each found to have plaques suspicious for malignancy, later demonstrated on histopathologic examination to be verruciform xanthoma. We discuss the connection between these severe genodermatoses and the suspected pathophysiology of verruciform xanthoma. In addition, we highlight the importance of recognizing verruciform xanthoma as a clinical mimicker of squamous cell carcinoma, for which patients with RDEB and KID syndrome are at increased risk.

Duke Scholars

Published In

Pediatr Dermatol

DOI

EISSN

1525-1470

Publication Date

January 2020

Volume

37

Issue

1

Start / End Page

176 / 179

Location

United States

Related Subject Headings

  • Xanthomatosis
  • Warts
  • Skin Neoplasms
  • Male
  • Keratitis
  • Humans
  • Female
  • Epidermolysis Bullosa Dystrophica
  • Diagnosis, Differential
  • Dermatology & Venereal Diseases
 

Citation

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MLA
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Evan-Browning, E., Rork, J., O’Donnell, P., Elaba, Z., Deng, A., & Wiss, K. (2020). Verruciform xanthoma in recessive dystrophic epidermolysis bullosa and keratitis-ichthyosis-deafness syndrome: Report of two cases and a review of the literature. Pediatr Dermatol, 37(1), 176–179. https://doi.org/10.1111/pde.14046
Evan-Browning, Eric, Jillian Rork, Patrick O’Donnell, Zendee Elaba, April Deng, and Karen Wiss. “Verruciform xanthoma in recessive dystrophic epidermolysis bullosa and keratitis-ichthyosis-deafness syndrome: Report of two cases and a review of the literature.Pediatr Dermatol 37, no. 1 (January 2020): 176–79. https://doi.org/10.1111/pde.14046.
Evan-Browning, Eric, et al. “Verruciform xanthoma in recessive dystrophic epidermolysis bullosa and keratitis-ichthyosis-deafness syndrome: Report of two cases and a review of the literature.Pediatr Dermatol, vol. 37, no. 1, Jan. 2020, pp. 176–79. Pubmed, doi:10.1111/pde.14046.
Evan-Browning E, Rork J, O’Donnell P, Elaba Z, Deng A, Wiss K. Verruciform xanthoma in recessive dystrophic epidermolysis bullosa and keratitis-ichthyosis-deafness syndrome: Report of two cases and a review of the literature. Pediatr Dermatol. 2020 Jan;37(1):176–179.
Journal cover image

Published In

Pediatr Dermatol

DOI

EISSN

1525-1470

Publication Date

January 2020

Volume

37

Issue

1

Start / End Page

176 / 179

Location

United States

Related Subject Headings

  • Xanthomatosis
  • Warts
  • Skin Neoplasms
  • Male
  • Keratitis
  • Humans
  • Female
  • Epidermolysis Bullosa Dystrophica
  • Diagnosis, Differential
  • Dermatology & Venereal Diseases