Case report: multiple keratocystic odontogenic tumour in a non-syndromal pediatric patient

Ozkan L., Aksoy S., ORHAN K., Cetiner S., Uyanik L. O., Buhara O., ...Daha Fazla

EUROPEAN JOURNAL OF PAEDIATRIC DENTISTRY, cilt.15, sa.2, ss.241-244, 2014 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 15 Sayı: 2
  • Basım Tarihi: 2014
  • Dergi Adı: EUROPEAN JOURNAL OF PAEDIATRIC DENTISTRY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.241-244
  • Anahtar Kelimeler: Keratocystic odontogenic tumour, Non-syndromal, RECURRENCE, MARSUPIALIZATION, ENUCLEATION, MANAGEMENT, DIAGNOSIS, CYST
  • Ankara Üniversitesi Adresli: Evet

Özet

Background Kerato cystic odontogenic tumour (KCOT) is an odontogenic tumour which stems from the odontogenic organs mostly localised in the lower jaw, particularly posterior body and ascending ramus of the mandible. The majority of these tumours are single lesions. When detected in the jaw in multiple forms, these cysts are seen in association with Gorlin Goltz/Basal cell naevus syndrome. However a few cases of non-syndromal multiple keratocystic odontogenic tumour have been reported in the literature.