Multiple hereditary infundibolocystic basal cell carcinoma: report of a sporadic case with a novel pathogenic germline variant in <i>SUFU</i>
Dear Editor, Germline loss-of-function variants in SUFU (MIM*607035), a component of the Hedgehog (HH) signaling pathway, have been associated with multiple hereditary infundibulocystic basal cell carcinoma (iBCC, MIM#604451). This is a yet undefined clinicopathological entity with features that are often distinct from basal cell nevus syndrome (BCNS, MIM#109400). In carriers of germline SUFU variants, basaloid neoplasms tend to arise at a later age compared with BCNS; the iBCC subtype is more frequently observed, and jaw cysts have not been reported. [...].
Authors
- Laura Eibenschutz (ORCID: https://orcid.org/0000-0002-2131-5875)
- Giovanna Floriddia (ORCID: https://orcid.org/0000-0003-0804-8730)
- Luca Fania (ORCID: https://orcid.org/0000-0003-4194-932X)
- Daniele Castiglia (ORCID: https://orcid.org/0000-0003-3501-6742)
- Vito Enzo Gomes
- Barbara Bellei (ORCID: https://orcid.org/0000-0002-3883-5500)
- Giulia Pascolini
Institutions
- Istituto Dermopatico dell'Immacolata (IT)
- San Gallicano Hospital (IT)
Publication Details
- Journal
- Dermatology Reports
- Published
- 2026-02-04
- DOI
- https://doi.org/10.4081/dr.2026.10662
- Primary Topic
- Hedgehog Signaling Pathway Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Ministero della Salute