Unicystic ameloblastoma of mandible. Report of 2 cases.
نویسندگان
چکیده
منابع مشابه
Multilocular Unicystic Ameloblastoma of Mandible
Introduction. We report a rare case of unicystic ameloblastoma (UA) of mandible which showed multilocular radiolucency on the left side of mandible on radiographic examination which is very unusual, and the majority of the cases of UAs till date has been reported of unilocular radiolucency. On histopathological examination, an odontogenic cystic lining that proliferates that intraluminally rese...
متن کاملUnicystic ameloblastoma of the mandible.
The aim of this work was to describe a case of unicystic ameloblastoma located in the left posterior mandibular body and angle of a 14-year-old Caucasian male. The tumour was described at clinical and histological level; moreover, its histopathological phenotype was depicted. Finally, the problems of differential diagnosis with odontogenic or congenital cyst and the most appropriate therapeutic...
متن کاملUnicystic ameloblastoma of the mandible - an unusual case report and review of literature
Ameloblastoma is a true neoplasm of odontogenic epithelial origin. It is the second most common odontogenic neoplasm, and only odontoma outnumbers it in reported frequency of occurrence. Its incidence, combined with its clinical behavior, makes ameloblastoma the most significant odontogenic neoplasm. Unicystic ameloblastoma (UA) refers to those cystic lesions that show clinical, radiographic, o...
متن کاملUnicystic Mural Ameloblastoma: An Unusual Case Report
Ameloblastoma is a benign odontogenic neoplasm which frequently affects the mandible. The term ameloblastoma includes several clinicoradiological and histological types. Apart from the most commonly encountered clinicopathologic models, there are few variants, whose biological profile is unknown or not elicited. Among these types, unicystic ameloblastoma is the least encountered variant of the ...
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ژورنال
عنوان ژورنال: Journal of Japan Society for Oral Tumors
سال: 1999
ISSN: 0915-5988,1884-4995
DOI: 10.5843/jsot.11.122