2015
DOI: 10.1371/journal.pone.0117789
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Incidence and Overall Survival of Malignant Ameloblastoma

Abstract: BackgroundMalignant ameloblastoma, comprising metastasizing ameloblastoma and ameloblastic carcinoma, represents 1.6–2.2% of all odontogenic tumors. Due to its rare nature, malignant ameloblastoma has only been reported in the literature in small case series or case reports. Using the Surveillance, Epidemiology and End-Results (SEER) database, we have performed a population-based study to determine the incidence rate and the absolute survival of malignant ameloblastoma.MethodUsing the International Classificat… Show more

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Cited by 56 publications
(49 citation statements)
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References 25 publications
(23 reference statements)
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“…[4] Additionally, malignant ameloblastomas, which can arise de novo or from a preexisting ameloblastoma, occur in 1.6%-2.2% of all ameloblastomas. [5] Ameloblastic carcinomas arising from peripheral ameloblastomas are exceedingly rare, with only approximately eleven cases of peripheral ameloblastic carcinoma having been reported to date, including one case of an initially benign appearing peripheral ameloblastoma recurring as ameloblastic carcinoma. [4,[6][7][8][9][10] Although there have been no prior studies demonstrating the relationship between non-Hodgkin lymphoma or radiation and the development of peripheral ameloblastoma, a retrospective study evaluating 322 non-Hodgkin lymphoma cases found a significantly increased risk for head and neck cancers among patients receiving radiation therapy for early-stage non-Hodgkin lymphoma.…”
Section: Discussionmentioning
confidence: 99%
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“…[4] Additionally, malignant ameloblastomas, which can arise de novo or from a preexisting ameloblastoma, occur in 1.6%-2.2% of all ameloblastomas. [5] Ameloblastic carcinomas arising from peripheral ameloblastomas are exceedingly rare, with only approximately eleven cases of peripheral ameloblastic carcinoma having been reported to date, including one case of an initially benign appearing peripheral ameloblastoma recurring as ameloblastic carcinoma. [4,[6][7][8][9][10] Although there have been no prior studies demonstrating the relationship between non-Hodgkin lymphoma or radiation and the development of peripheral ameloblastoma, a retrospective study evaluating 322 non-Hodgkin lymphoma cases found a significantly increased risk for head and neck cancers among patients receiving radiation therapy for early-stage non-Hodgkin lymphoma.…”
Section: Discussionmentioning
confidence: 99%
“…[12,13] Peripheral ameloblastomas vary in size but are usually limited to the gingiva without invading the underlying bone. [5] Differential diagnosis includes peripheral giant cell granuloma, peripheral odontogenic fibroma, peripheral ossifying fibroma, papilloma, pyogenic granuloma, epulis, and fibroma. [13][14][15] Radiological examination may demonstrate superficial cortical bone erosion or depression, which are known as "cupping" or "saucerization".…”
Section: Discussionmentioning
confidence: 99%
“…MA represents 1.6-2.2% of all odontogenic tumors (8). There is one report, by Rizzitelli et al in 2014, on the incidence of MA and its survival rate (9). Unfortunately, that study did not calculate the rate of MA and AC separately; instead, they were calculated as a single percentage.…”
Section: Discussionmentioning
confidence: 99%
“…The overall survival rate is 17.6 years -despite being metastatic, the disease has an indolent course. The peak incidence is between the third and fifth decade (9).…”
Section: Discussionmentioning
confidence: 99%
“…Malignant odontogenic tumors with the histological features of ameloblastoma represent 1.6–2.2% of all odontogenic tumors (1), and may be classified as metastasizing ameloblastoma or ameloblastic carcinoma (AC); it is generally agreed that the term ‘malignant ameloblastoma’ refers to tumors exhibiting features of a benign ameloblastoma, while the term ‘ameloblastic carcinoma’ indicates tumors that are still recognizable as ameloblastoma but possess histological features of malignancy. AC, which seems to be more frequent than malignant ameloblastoma (2), is considered to be a rare tumor, as few cases have been published.…”
Section: Introductionmentioning
confidence: 99%