SavedAdd your journal

Journals / Tanısal ve Girişimsel Radyoloji (Yeni Adı: Dİagnostic & Intervent. Radiol) / 2004 / Cilt: 10 - Sayı: 4

Gorlin syndrome with osteoma in the maxillary sinus (Case report)

Gorlin sendromu: Radyolojik bulgular

Halil SEVİNÇ
Mustafa ÖZTÜRK
Ertuğrul MAVİLİ
İRFAN ÖZYAZGAN
Pages
268–271
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

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.

📌 3 Key Takeaways

🎯
Objective & Hypothesis: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.
📊
Key Findings & Data:Many associated lesions have been reported.
💡
Conclusion & Impact: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.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Osteoma · Bazal hücreli nevus sendromu · Radyoloji

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.

Özet

Gorlin sendromu deride bazal hücreli karsinom, çenede odontojenik keratokist, değişik iskelet sistemi anomalileri ve lameller falks kalsifikasyonları ile karakterize otozomal dominant geçişli klinik bir antitedir (1,2). İlgili gen 9q22.3-q31 kromozom lokalizasyonundadı r (3). Gorlin sendromu ile ilişkili olarak değişik sistemlere ait çok sayıda anomali bildirilmiştir (4). Bu çalışmada, Gorlin sendromu bulgularına ilave olarak maksiller sinüsünde osteomu bulunan bir kadın olgu sunulmuştur.

🔖

Cite This Article

SEVİNÇ, H., ÖZTÜRK, M., MAVİLİ, E., ÖZYAZGAN, İ. (2004). Gorlin syndrome with osteoma in the maxillary sinus (Case report). Tanısal ve Girişimsel Radyoloji (Yeni Adı: Dİagnostic & Intervent. Radiol), Cilt: 10 - Sayı: 4, 268–271. https://ajindex.com/articles/364236

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (10)

  1. Gorlin RJ, Goltz RW. Multiple nevoid basal cell epithelioma, jaw cysts and bifid rib syndrome. N Engl J Med 1960; 262:908- 912
  2. Gorlin RJ, Vickers RA, Kelln E, Williamson JJ. The multiple basal-cell nevi syndrome. Cancer 1965; 18:89-110
  3. Farndon PA, Del Mastro FG, Evans DGR, Kilpatrick MW. Location of gene for Gorlin syndrome. Lancet 1992; 339:581-582
  4. Neblett CR, Waltz TA, Anderson DE. Neurological involvement in the nevoid basal cell carcinoma syndrome. J Neurosurg 1971; 35:577-584
  5. Schultz SM, Twickler DM, Wheeler DE, Hogan TD. Ameloblastoma associated with basal cell nevus (Gorlin) syndrome: CT findings. J Comput Assist Tomogr 1987; 11:901-904
  6. Mills J, Foulkes J. Gorlin syndrome: a radiological and cytogenetic study of nine cases. Br J Radiol 1967; 40:366-371
  7. Evans DGR, Ladusans EJ, Rimmer S, Burnell LD, Thakker N, Farndon PA. Complications of the naevoid basal cell carcinoma syndrome: results of a population based study. J Med Genet 1993; 30:460-464
  8. Lovin JD, Talarico CL, Wegert SL, Gaynor LF, Sutley SS. Gorlin’s syndrome with associated odontogenic cysts. Pediatr Radiol 1991; 21:584-587
  9. Iwanaga S, Shimoura H, Shimuzu M, Numaguchi Y. Gorlin syndrome: unusual manifestations in the sella turcica and the sphenoidal sinus. AJNR Am J Neuroradiol 1998; 19:956-958
  10. Harnsberger HR. Handbook of Head and Neck Imaging. 2nd ed. St. Louis: Mosby, 1995; 384-385.