1998
DOI: 10.1016/s0278-2391(98)90118-5
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Ameloblastic fibroma in a 7-week-old infant: A case report and review of the literature

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Cited by 37 publications
(36 citation statements)
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“…Lysell and Sund [13] proposed the incomplete primary removal as a reason of recurrence in their cases. This was supported by Mosby et al [14] explaining that after the complete removal of a tumour clinically, this could not be stated at a cellular level. They suggested conservative removal of AF and modified block resection of any recurrence.…”
Section: Discussionmentioning
confidence: 80%
“…Lysell and Sund [13] proposed the incomplete primary removal as a reason of recurrence in their cases. This was supported by Mosby et al [14] explaining that after the complete removal of a tumour clinically, this could not be stated at a cellular level. They suggested conservative removal of AF and modified block resection of any recurrence.…”
Section: Discussionmentioning
confidence: 80%
“…Ameloblastic fibroma is a rare tumor, accounting for only 2.5% of odontogenic tumors 2,5) . The average age of presentation is in the teenage years 2,5) .…”
Section: ⅲ Discussionmentioning
confidence: 99%
“…AF exhibits somewhat slow clinical growth, is well encapsulated and shows an innocuous benign behavior, according to most studies [3][4][5] . A conservative treatment strategy, such as enucleation and curettage, is generally the treatment of choice, and the prognosis of these tumors is reported to be good 3,5) .…”
Section: ⅰ Introductionmentioning
confidence: 99%
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“…AF has been reported in patients aged 7 weeks to 51 years (6,7), but the tumor is considered a tumor of childhood and adolescence and occur almost exclusively in the first and second decades of life (6,(8)(9)(10)(11)(12)(13). In the majority of cases, the lesion arises in the mandible and patients present as a slow-growing, painless lesion and/or failure of the tooth eruption (8)(9)(10)(11)(12).…”
Section: Introductionmentioning
confidence: 99%