A case of Gorlin syndrome like phenotype with multiple infundibulocystic basal cell carcinomas in a moniliform blepharosis arrangement

David Petrosian; Paloma Reiter; Suzanne Sirota Rozenberg; Sergey Petrosian

doi:10.1016/j.jdcr.2023.01.025

A case of Gorlin syndrome like phenotype with multiple infundibulocystic basal cell carcinomas in a moniliform blepharosis arrangement

JAAD Case Rep. 2023 Feb 11:34:27-31. doi: 10.1016/j.jdcr.2023.01.025. eCollection 2023 Apr.

Authors

David Petrosian¹, Paloma Reiter², Suzanne Sirota Rozenberg², Sergey Petrosian³

Affiliations

¹ Department of Family Medicine, St. John's Episcopal Hospital, Far Rockaway, New York.
² Department of Dermatology, St. John's Episcopal Hospital, Far Rockaway, New York.
³ Ronald O. Perelman Department of Dermatology, New York University School of Medicine, New York, New York.

No abstract available

Keywords: BCC, basal cell carcinoma; BCNS, basal cell nevus syndrome; Gorlin syndrome; IBCC, infundibulocystic basal cell carcinoma; MHIBCC, multiple hereditary infundibulocystic basal cell carcinoma syndrome; PTCH, patched tumor suppressor; SUFU; SUFU, suppressor of fused homolog; VUS, variant of uncertain significance; basal cell nevus syndrome; dermoscopy; eyelid margin; infundibulocystic basal cell carcinoma; moniliform blepharosis; multiple hereditary infundibulocystic basal cell carcinoma syndrome; nevoid basal cell carcinoma syndrome; novel SUFU gene; variant of uncertain significance.

Publication types

Case Reports