Koparal M.Alan H.Ağaçayak K.S.Erdoğdu I.H.Gulsun B.2024-08-042024-08-0420172146-2852https://doi.org/10.7126/CUMUDJ.345921https://hdl.handle.net/11616/91903Central giant cell tumours are rare, accounting for less than 7% of all jaw tumours. These tumours are usuallyobserved in women, occur most often in the mandible,and are more common in the second decade of life.Treatment consists of local removal, partial resection, ortotal resection. In this case, a 32-year-old female patientpresented in our clinic with pain in the anterior mandible.No cervical lymphadenopathy was detected uponphysical examination. No ulceration was observed duringthe intraoral examination, but sensitivity was found in thevestibular area. However, no sensation loss in any teethor in the lips was detected. This case report presents a 32-year-old female patient with central giant cell tumourcausing extensive bone loss in the mandible base that wastreated with partial resection © 2017. Cumhuriyet Dental Journal. All Rights Reserved.eninfo:eu-repo/semantics/openAccessGiant cell granulomaMandibleResectionCOMBINED TREATMENT OF A LARGE AGGRESSIVE CENTRAL GIANT CELL GRANULOMA (CASE REPORT)Büyük Agresif Bir Santral Dev Hücreli Granuloma Birlikte Tedavisi (Olgu Sunumu)Article202858910.7126/CUMUDJ.3459212-s2.0-85123020797Q4