Keratocystic Odontogenic Tumor Involving Coronoid Process and Condyle

Uday Shankar Yaga, Prashanth Panta, Ashwini Kumar Mengji, B. Radhika, Swetha Soankamble, Swathi Esther, S. Imran, T. Reddy
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Abstract

Keratocystic odontogenic tumor (KCOT) is a peculiar entity affecting the jaw bones. It is a benign intraosseous neoplasm of jaws that shows a very high recurrence rate. It is locally aggressive and is lined by keratinized stratified squamous epithelium. The most important feature that separates KCOTs and other odontogenic cysts and tumors is the presence of microcysts also called as daughter cysts. Daughter cysts are the main source of recurrence, and they complicate the treatment plan to a great extent. KCOT is commonly seen in the posterior mandible and ramus area and rarely the condyle. In this paper, we present the case of a 25 year old female patient with KCOT involving the condyle and coronoid process along with relevant review of literature. This patient was subjected to marsupialisation, and is followed up once in 3 months.
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累及冠突和髁的角化囊性牙源性肿瘤
角化囊性牙源性肿瘤(KCOT)是一种影响颌骨的特殊肿瘤。它是一种良性颌骨骨内肿瘤,复发率非常高。它是局部侵袭性的,由角化的层状鳞状上皮排列。区分kcot与其他牙源性囊肿和肿瘤的最重要特征是存在微囊肿,也称为子囊肿。子囊肿是复发的主要原因,在很大程度上使治疗方案复杂化。KCOT常见于下颌骨后支区,很少见于髁突。在本文中,我们提出了一个25岁的女性患者KCOT累及髁突和冠突的病例,并对相关文献进行了复习。该患者接受有袋化手术,每3个月随访1次。
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