2015
DOI: 10.1016/j.oooo.2015.05.011
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Adenoid ameloblastoma: clinicopathologic description of five cases and systematic review of the current knowledge

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Cited by 42 publications
(66 citation statements)
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“…Perhaps, many cases of AAD might be overlooked by pathologists as AM or AOT depending on the predominance of either entity in the microscopic examination. This possibility is supported by the fact that 4/45 cases of AM were re-assessed and re-classified as AAD in a retrospective study by Loyola et al [13]. Therefore, the actual number of cases might be much greater than those reported in the literature.…”
Section: Resultsmentioning
confidence: 96%
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“…Perhaps, many cases of AAD might be overlooked by pathologists as AM or AOT depending on the predominance of either entity in the microscopic examination. This possibility is supported by the fact that 4/45 cases of AM were re-assessed and re-classified as AAD in a retrospective study by Loyola et al [13]. Therefore, the actual number of cases might be much greater than those reported in the literature.…”
Section: Resultsmentioning
confidence: 96%
“…Adorno-Farias et al demonstrated pseudoducts with PAS-positive material [24]. Loyola et al [13] stated that although basophilic mucoid material may be observed within the duct-like spaces, secretory component was not detected. In the most recent case of AAD reported by Arruda et al, Alcian blue staining revealed a significant amount of basophilic material and scarce PAS-positive eosinophilic material in duct-like spaces, indicating its mucoid nature [25].…”
Section: Resultsmentioning
confidence: 99%
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“…In 2015, a more recent article by Loyola et al brought adenoid ameloblastoma to the forefront presenting 5 additional cases and, to date, less than 40 cases have been reported with numerous reports occurring in the last five years [28][29][30][31][32][33][34][35][36][37][38][39][40][41][42]. Given the small number of cases, it is difficult to draw conclusions, but these tumors appear to present in a wide age range (19-79, mean 43 years), as large tumors with a mean size of 4.4 cm, with a maxillary predilection (67%), and have a relatively high recurrence rate (10/13, 77%) [28,[32][33][34][35][36][37][38][39][40][41][42]. The histologic features include a cribriform architecture with duct-like structures, peripheral columnar cells with reverse polarity, clear cells, ghost cells (that may calcify), variable amounts of dentinoid/ osteoid, increased mitotic activity, pseudopapillary areas, and distinctive whorls/morules ( Fig.…”
Section: Uncommon/diagnostically Challenging Odontogenic Tumorsmentioning
confidence: 99%