Odontogenic keratocysts in the Basal Cell Nevus (Gorlin-Goltz) Syndrome associated with paresthesia of the lower jaw: Case report, retrospective analysis of a representative Czech cohort and recommendations for the early diagnosis
Jazyk angličtina Země Švédsko Médium print
Typ dokumentu kazuistiky, časopisecké články
PubMed
27857042
PII: NEL370416C02
Knihovny.cz E-zdroje
- MeSH
- anodoncie diagnostické zobrazování etiologie MeSH
- časná diagnóza MeSH
- čelisti diagnostické zobrazování MeSH
- dítě MeSH
- duplikace genu MeSH
- kohortové studie MeSH
- kojenec MeSH
- lidé MeSH
- mladiství MeSH
- odontogenní cysty diagnostické zobrazování etiologie MeSH
- parestezie etiologie MeSH
- počítačová rentgenová tomografie MeSH
- předškolní dítě MeSH
- receptor Patched 1 genetika MeSH
- rentgendiagnostika panoramatická MeSH
- retrospektivní studie MeSH
- sekvenční analýza DNA MeSH
- směrnice pro lékařskou praxi jako téma MeSH
- syndrom bazocelulárního névu komplikace diagnóza genetika MeSH
- zobrazování trojrozměrné MeSH
- Check Tag
- dítě MeSH
- kojenec MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- Geografické názvy
- Česká republika MeSH
- Názvy látek
- PTCH1 protein, human MeSH Prohlížeč
- receptor Patched 1 MeSH
OBJECTIVES: Identification of early presenting signs of the Basal Cell Nevus (BCNS; synonyme Gorlin-Goltz) syndrome, which is associated with a principal triad of multiple basal cell nevi, jaw odontogenic keratocysts, and skeletal anomalies, in stomatological and neurological practices. Proposal of multidisciplinary diagnostic algorithm comprising other medical specialists, including pathology, imaging, laboratory and molecular analyses based on the study outcomes. DESIGN: Case report of a male patient reporting paresthesia of their lower jaw, with right facial asymmetry (maxilla and mandible) and radiological detection of large osteolytic lesions in both jaws, including a retrospective analysis of a representative Czech cohort with BCNS from within the last decade. SETTING: Clinical, imaging and laboratory analyses were carried out at a national tertiary centre. RESULTS: A multidisciplinary clinical approach followed by surgical management lead to the identification of odontogenic cysts, which were substantiated by histological examination. DNA sequencing of the PTCH1 gene detected a c.2929dupT resulting in p. Tyr977Leufs*16 pathogenic variant. This finding confirmed the clinical and laboraoty diagnosis of BCNS. Parental DNA analysis showed that this causal genetic defect arose de novo. Surgical management and orthodontic therapy were successful. CONCLUSIONS: Analysis of the reported case and retrospective data analysis provided evidence that paresthesia of the lower jaw should be considered as one of the early presenting signs of this rare disorder in stomatological and neurological practice. Obtained results allowed us to formulate recommendations for diagnostic practice in stomatology and neurology.