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<ArticleSet><Article><Journal><PublisherName>Isfahan University of Medical Sciences</PublisherName><JournalTitle>Dental Research Journal</JournalTitle><Issn>1735-3327</Issn><Volume>9</Volume><Issue>3</Issue><PubDate PubStatus="epublish"><Year>2012</Year><Month>08</Month><Day>21</Day></PubDate></Journal><ArticleTitle>Hemangiomatous ameloblastoma in maxilla: A report of a very rare case</ArticleTitle><FirstPage>1096</FirstPage><LastPage>1096</LastPage><Language>EN</Language><AuthorList><Author><FirstName>Vivek</FirstName><LastName>Kumar Sharma</LastName></Author><Author><FirstName>Sanjeev</FirstName><LastName>K. Verma</LastName></Author><Author><FirstName>Lata</FirstName><LastName>Goyal</LastName><Affiliation>Department of Periodontics and Community Dentistry, Dr. Z. A. Dental College, Aligarh&#13;
Muslim University, Aligarh, Uttar Pradesh, India. latagoyal83@gmail.com</Affiliation></Author><Author><FirstName>Prabhat</FirstName><LastName>Kumar Chaudhary</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2012</Year><Month>08</Month><Day>21</Day></PubDate></History><Abstract>Hemangiomatous ameloblastoma (HA), which is a rare ameloblastic variant, is presented in a15-year-old boy in the maxillary right molar region associated with unerupted canine and premolars.Radiologic and computed tomographic analysis was suggestive of cystic lesion. An histology pictureconfirmed the diagnosis of HA. There are less than eight cases documented in the literature andmostly are in the middle age with mandibular location. This is first ever reported case of HA ina 15-year-old boy with maxillary location. Due to less number of documented cases and no longtermfollow-ups, clinical behavior and prognosis of this lesion are uncertain. In this case report, theclinical, histological, and radiographic features of HA are presented.Key Words: Ameloblastoma variants, hemangiomas, unilocular radiolucency, vascularameloblastoma</Abstract></Article></ArticleSet>
