ODONTOGENIC KERATOCYST IN THE MAXILLA: CASE REPORT
DOI:
https://doi.org/10.5335/rfo.v28i1.14204Keywords:
Cisto Odontogênico, Síndrome de Gorlin-Goltz, Odontologia HospitalarAbstract
OJECTIVE: To report the process of diagnosis and treatment of an odontogenic keratocyst (QO) in the maxillary sinus and its importance in the investigation and diagnosis of Gorlin-Goltz Syndrome (GGS). CASE REPORT: A 20-year-old female patient presented at the Dentistry and Stomatology service, referred by the Medical Genetics team to investigate the presence of QO to define the diagnosis of GGS. The patient had only two criteria for the diagnosis of GGS, the diagnosis of multiple basal cell carcinomas (major criterion) and macrocephaly (minor criterion), and therefore, if the presence of OC was detected, GGS would be confirmed. Panoramic radiography was performed and the presence of alterations in the bone trabeculae in the maxillary tuberosity on the left side was verified. For this reason, computed tomography of the maxillary sinuses was also requested and a well-defined lesion was found, occupying almost completely the left maxillary sinus in close contact with the root of tooth 27. Therefore, an incisional biopsy of the lesion was performed, accompanied by puncture of the same. In the puncture, a characteristic caseous content suggestive of keratin was obtained. The histopathological report of the lesion was described by the pathologist as an odontogenic cyst. With this, tooth extraction procedures for tooth 27 and enucleation of the lesion in the maxillary sinus were carried out by the dentistry and otorhinolaryngology teams, respectively, in a surgical center. The histopathological report confirmed the presence of QO, so it was possible to confirm the diagnosis of GGS by the medical genetics team. The patient showed no signs of recurrence or new QO after 2 years of the procedure. FINAL CONSIDERATIONS: GGS requires special dental attention, given the high rate of QO in patients with this syndrome. A thorough dental examination involving clinical examination and radiographic examinations should be performed at follow-up visits.
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References
Padma P, Jayanthi K, Mahesh D. Gorlin-Goltz Syndrome. Case Rep Dent. 2012; 4(2): 279-282.
Guerra LAP, Silva PF, Santos RLO, Silva AMF, Albuquerque DA. Conservative treatment of multiple odontogenic tumors in patients ceratocistics non-syndromic. Rev. Cir. Traumatol. Buco-Maxilofac. 2013; 13(2):43-50.
Silva LP, Rolim LSA, Silva LAB, Pinto LP, Souza LB. The recurrence of odontogenic keratocysts in pediatric patients is associated with clinical findings of Gorlin-Goltz Syndrome. Med Oral Patol Oral Cir Bucal. 2020; 25(1): e56–e60.
Manfredi, M., et al., Nevoid basal cell carcinoma syndrome: a review of the literature. Int J Oral Maxillofac Surg, 2004; 33(2):117-24.
Nilius M, Kohlhase J, Lorenzen J, Lauer G, Schulz MC. Multidisciplinary oral rehabilitation of an adolescent suffering from juvenile Gorlin-Goltz syndrome – a case report. Head Face Med. 2019; 15:5.
MaÅ‚gorzata Kiwilsza, Katarzyna Sporniak-Tutak. Gorlin-Goltz syndrome – a medical condition requiring a multidisciplinary approach. Med Sci Monit. 2012; 18(9):RA145–RA153.
Ortega-García-de Amezaga A, García-Arregui O, Zepeda-Nuño S, Acha-Sagredo A, Aguirre-Urizar JM. Gorlin-Goltz syndrome: Clinicopathologic aspects. Med Oral Patol Oral Cir Bucal. 2008;13(6):E338-43.
Augusto Neto RT, Gabrielli MAC, Gabrielli MFR, Monnazzi MS, Gorla LFO, Costa RR. Tratamento de queratocisto em ângulo e corpo mandibular, apresentando recidiva após 14 meses. Rev Odontol UNESP. 2014; 43(N Especial):196.
Silva EGP, Bedin GL, Brandão BJF. Síndrome de Gorlin-Goltz - Diagnóstico clínico. BWS Journal. 2021; 4:1-7.
Gorlin RJ, Goltz RW. Multiple nevoid basal-cell epithelioma, jaw cysts and bifid rib. A syndrome. N Engl J Med. 1960; 262:908-12.
Chan JKC, El-Naggar AK, Grandis JR, Takata T, Slootweg PJ. WHO Classification of Head and Neck Tumours. World Health Organization, 4th edition; 2017.
Barnes L, Eveson JW, Reichart P, Sidransky D. Pathology and genetics of head and neck tumours. WHO/IARC Classification of Tumours, 3rd edition; 2005.
Tolentino ES. Nova classificação da OMS para tumores odontogênicos: o que mudou? Updated WHO classification for odontogenic tumors: what has changed? RFO. 2018; 23 (1):119-123.
Mendes-Abreu J, Pinto-Gouveia M, Tavares-Ferreira C, Brinca A, Vieira R. Síndrome de Gorlin-Goltz: Diagnóstico e Hipóteses de Tratamento. Acta Médica Portuguesa, 2017; 30(5):418.
Neville BW, Damm DD, Allen CM. et al. Patologia Oral & Maxilofacial. Rio de Janeiro, Guanabara Koogan, 2004.
Pogrel MA, Jordan RCK. Marsupialization as a definitive treatment for the odontogenic Keratocyst. J Oral Maxillofac Surg. 2004; 62(6):651-55.
Chandran S, Marudhamuthu K, Riaz R, Balasubramaniam S. Odontogenic keratocysts in Gorlin–Goltz syndrome: A case report. J Int Oral Health. 2015; 7(1):76-79.
Spadari, F., Pulicari, F., Pellegrini, M. et al. Multidisciplinary approach to Gorlin-Goltz syndrome: from diagnosis to surgical treatment of jawbones. Maxillofac Plast Reconstr Surg. 2022; 44(1):25.
Borghesi A, Nardi C, Giannitto C, Tironi A, Maroldi R, Di Bartolomeo F, Preda L. Odontogenic keratocyst: imaging features of a benign lesion with an aggressive behaviour. Insights Imaging. 2018; 9(5):883-897
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