dc.contributor.author |
Robinson, Liam
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|
dc.contributor.author |
Abreu, Lucas Guimaraes
|
|
dc.contributor.author |
Fonseca, Felipe Paiva
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|
dc.contributor.author |
Hunter, K.D. (Keith)
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|
dc.contributor.author |
Ambele, Melvin Anyasi
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|
dc.contributor.author |
Van Heerden, Willem Francois Petrus
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|
dc.date.accessioned |
2024-08-07T07:34:00Z |
|
dc.date.available |
2024-08-07T07:34:00Z |
|
dc.date.issued |
2024-03 |
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dc.description |
DATA AVAILABILITY STATEMENT : The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions. |
en_US |
dc.description |
SUPPLEMENTARY TABLE 1. Data from included studies. |
en_US |
dc.description.abstract |
BACKGROUND :
Ameloblastic carcinoma (AC) is the most common odontogenic malignancy, constituting approximately 30% of cases in this category. Literature is sparse on malignant odontogenic neoplasms, with a large proportion of current knowledge derived from case reports or small case series.
METHODS :
A systematic review of case series/case reports of AC was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) Statement guidelines. Demographic and clinical information, including duration of the lesion, location, clinical presentation and radiologic features, were analysed. Additionally, the origin of the lesion (primary/secondary), Ki-67 proliferation index, treatment performed, metastasis, tumour recurrence and prognosis were collected for analysis.
RESULTS :
A total of 126 studies, including 285 individual cases of AC, were included in this review. Patients presented with a near-equal distribution of painless and painful swellings. ACs presented at a median age of 45 years, with a male-to-female ratio of 1:2. The mandible was most frequently involved, with rare cases extending to involve more than one region, including crossing the midline. Although most lesions presented with poorly-demarcated borders (52.6%), unilocular lesions with well-demarcated borders (47.4%) comprised a substantial number in the sample. The proliferation index was only reported in 27 cases, with a mean score of 42% and a wide range. The probability of tumour recurrence increased, and the survival probability decreased with prolonged follow-up duration.
CONCLUSION :
This study provides more comprehensive, up-to-date descriptive data on these rare odontogenic malignancies, aiding clinicians and Pathologists with the diagnosis and surgeons in their management of cases. |
en_US |
dc.description.department |
Oral Pathology and Oral Biology |
en_US |
dc.description.librarian |
hj2024 |
en_US |
dc.description.sdg |
SDG-03:Good heatlh and well-being |
en_US |
dc.description.uri |
http://wileyonlinelibrary.com/journal/jop |
en_US |
dc.identifier.citation |
Robinson, L., Abreu, L.G., Fonseca, F.P., Hunter, K.D., Ambele, M.A. & Van Heerden, W.F.P. Ameloblastic carcinoma: A systematic review. Journal of Oral Pathology and Medicine 2024; 53 (3) : 174‐181. doi: 10.1111/jop.13517. |
en_US |
dc.identifier.issn |
0904-2512 (print) |
|
dc.identifier.issn |
1600-0714 (online) |
|
dc.identifier.other |
10.1111/jop.13517. |
|
dc.identifier.uri |
http://hdl.handle.net/2263/97477 |
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dc.language.iso |
en |
en_US |
dc.publisher |
Wiley |
en_US |
dc.rights |
© 2024 The Authors. Journal of Oral Pathology & Medicine published by John Wiley & Sons Ltd.
This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License. |
en_US |
dc.subject |
Ameloblastic carcinoma |
en_US |
dc.subject |
Preferred reporting items for systematic review and meta-analysis (PRISMA) |
en_US |
dc.subject |
Head and neck cancer |
en_US |
dc.subject |
Odontogenic neoplasms |
en_US |
dc.subject |
Recurrence rates |
en_US |
dc.subject |
Survival probability |
en_US |
dc.subject |
SDG-03: Good health and well-being |
en_US |
dc.title |
Ameloblastic carcinoma : a systematic review |
en_US |
dc.type |
Article |
en_US |