Gorlin-Goltz-Syndrom

Masses of
developmental and genetic origin affecting the paediatric craniofacial skeleton. Typical manifestations of nevoid basal cell carcinoma syndrome (NBCCS) in a 16-year-old boy. a Orthopantomography (OPT) shows cystic lesions of the mandible and maxilla (arrows), with unilocular and multilocular pattern and smooth or scalloped borders associated with displaced and unerupted permanent teeth. b Coronal CT scan (bone window) shows ectopic calcifications of the falx cerebri and tentorium cerebelli (arrows) and spotted meningeal calcifications (arrowheads). Brain MRI reveals a cavum veli interpositi on axial T2 (asterisk in c) and coronal contrast-enhanced T1 (asterisk in d) and also vermian dysgenesis (arrowheads in d)
insightsimaging.springeropen.com • Open Access
Gorlin-Goltz
syndrome • Gorlin-Goltz syndrome - incidental posterior communicating aneurysm - Ganzer Fall bei Radiopaedia
Coulthard A, Gorlin-Goltz syndrome - incidental posterior communicating aneurysm. Case study, Radiopaedia.org (Accessed on 18 Nov 2022) https://doi.org/10.53347/rID-39078 • CC by-nc-sa 3.0 (modified)
nicht verwechseln mit: Goltz-Gorlin-Syndrom