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[Gorlin syndrome with osteoma in the maxillary sinus (case report)].

Authors
  • Sevinç, Halil
  • Oztürk, Mustafa
  • Mavili, Ertuğrul
  • Ozyazgan, Irfan
Type
Published Article
Journal
Tanısal ve girişimsel radyoloji : Tıbbi Görüntüleme ve Girişimsel Radyoloji Derneği yayın organı
Publication Date
Dec 01, 2004
Volume
10
Issue
4
Pages
268–271
Identifiers
PMID: 15611914
Source
Medline
License
Unknown

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.

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