Gorlin syndrome with osteoma in the maxillary sinus (case report) Gorlin sendromu: Radyolojik bulgular.


Sevinç H. , ÖZTÜRK M. , Mavili E., ÖZYAZGAN İ.

Tanisal ve girişimsel radyoloji : Tibbi Görüntüleme ve Girişimsel Radyoloji Dernegi yayin organi, vol.10, no.4, pp.268-271, 2004 (Refereed Journals of Other Institutions) identifier identifier

  • Publication Type: Article / Article
  • Volume: 10 Issue: 4
  • Publication Date: 2004
  • Title of Journal : Tanisal ve girişimsel radyoloji : Tibbi Görüntüleme ve Girişimsel Radyoloji Dernegi yayin organi
  • Page Numbers: pp.268-271

Abstract

Gorlin syndrome is a rare autosomal dominant disorder characterized by multiple basal cell carcinomas of the skin, odontogenic keratocysts of the jaw, various skeletal abnormalities, and lamellar falx calsifications. Many associated lesions have been reported. In this report, we present a case of Gorlin syndrome with an osteoma in the maxillary sinus which has never been reported in the literature.