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
APA
Chicago
ICMJE
MLA
NLM
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 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):176–9.
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.
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