Aithal D, Reddy B S, Mahajan S, Boaz K, Kamboj M
Department of Oral Pathology and Microbiology, College of Dental Surgery, Mangalore, India.
J Oral Pathol Med. 2003 Jul;32(6):376-8. doi: 10.1034/j.1600-0714.2003.00141.x.
Calcifying odontogenic cyst (COC) is an uncommon developmental odontogenic cyst first described by Gorlin in 1962. It is considered as extremely rare and accounts for only 1% of jaw cysts reported. Because of its diverse histopathology, there has always been confusion about its nature as a cyst, neoplasm or hamartoma. Several subclassifications have been proposed. Here, we present a case of calcifying odontogenic cyst with ameloblastic proliferation - an extremely rare histologic variant. The classical histologic features of the lining epithelium in the form of cords and presence of characteristic ghost cells were seen along with ameloblastomatous proliferations. Ameloblastomatous COC microscopically resembles unicystic ameloblastoma except for the ghost cells and calcifications within the proliferative epithelium. The nature of the COC is controversial. The case is presented here for its rarity, and difference between ameloblastomatous COC and ameloblastoma ex COC has been emphasized.
牙源性钙化囊肿(COC)是一种罕见的牙源性发育性囊肿,1962年由戈林首次描述。它被认为极为罕见,在报告的颌骨囊肿中仅占1%。由于其组织病理学表现多样,其作为囊肿、肿瘤或错构瘤的性质一直存在争议。已提出了几种亚分类。在此,我们报告一例伴有成釉细胞增生的牙源性钙化囊肿——一种极为罕见的组织学变异型。可见衬里上皮呈条索状的经典组织学特征以及特征性的影细胞,同时伴有成釉细胞瘤样增生。成釉细胞瘤样牙源性钙化囊肿在显微镜下类似于单囊性成釉细胞瘤,只是增生上皮内存在影细胞和钙化。牙源性钙化囊肿的性质存在争议。本文报告此病例是因其罕见性,并强调了成釉细胞瘤样牙源性钙化囊肿与成釉细胞瘤的区别。