Chaudhary Seema, Sinha Ashish, Barua Pranamee, Mallikarjuna Rachappa
Department of Pediatric Dentistry, Kothiwal Dental College and Research Centre, Moradabad, Uttar Pradesh, India.
BMJ Case Rep. 2013 Feb 20;2013:bcr2012008741. doi: 10.1136/bcr-2013-008741.
Keratocystic odontogenic tumours are known for their peculiar behaviour, varied origin, debated development, unique tendency to recur and disputed treatment modalities. Thus, it has been the subject of much research over the last 40 years. It was formerly known as odontogenic keratocyst (OKC). OKC received its new title as keratocystic odontogenic tumour (KCOT) by the WHO (2005) in order to suggest its aggressive and recurrent nature. KCOT is a benign intraosseous neoplasm of the jaw. Involvement of the maxillary sinus is an unusual presentation. We present the case of an 11-year-old child with extensive KCOT and an impacted canine in the right maxillary sinus. The cyst was initially misdiagnosed to be a dentigerous cyst based on the clinical and radiographic features though a differential diagnosis of KCOT and adenomatoid odontogenic tumour was made. The histological examination of the specimen finally confirmed it to be a KCOT. The clinical, radiological and histological features of this tumour along with its surgical management have been discussed.
牙源性角化囊性瘤以其独特的行为、多样的起源、有争议的发展、独特的复发倾向和有争议的治疗方式而闻名。因此,在过去40年里,它一直是众多研究的主题。它以前被称为牙源性角化囊肿(OKC)。为了表明其侵袭性和复发性,OKC在2005年被世界卫生组织重新命名为牙源性角化囊性瘤(KCOT)。KCOT是颌骨的一种良性骨内肿瘤。上颌窦受累是一种不常见的表现。我们报告一例11岁儿童,患有广泛的KCOT,且右上颌窦有一颗埋伏尖牙。根据临床和影像学特征,该囊肿最初被误诊为含牙囊肿,不过也对KCOT和腺样牙源性肿瘤进行了鉴别诊断。标本的组织学检查最终证实其为KCOT。本文讨论了该肿瘤的临床、放射学和组织学特征及其手术治疗。