ReviewHead and neck pathology2022
Diagnostic Enigma of Adenoid Ameloblastoma: Literature Review Based Evidence to Consider It as a New Sub Type of Ameloblastoma.
Review in Head and neck pathology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.
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Who cites it
19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 39 citations in OpenAlex.
- A Systematic Review of Adenoid Ameloblastoma: A Newly Recognized Entity.Head and neck pathology · 2023Pooled it
- Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Odontogenic and Maxillofacial Bone Tumours.Head and neck pathology · 2022Pooled it
- Evidence from intra-patient progression indicates adenoid ameloblastoma as a phenotypic variant of dentinogenic ghost cell tumor.Virchows Archiv : an international journal of pathology · 2026Article
- Adenoid ameloblastoma of the mandible: report of a new case of a distinct type of odontogenic neoplasms.BMC oral health · 2026Article
- Adenoid ameloblastoma: Conservative approach in a rare odontogenic lesion.Oral and maxillofacial surgery · 2026Article
- Adenoid Ameloblastoma: A Case Report on this Newly Recognized Under-Treated Odontogenic Tumour.Journal of maxillofacial and oral surgery · 2025Article
- Article
- Ameloblastoma with adenoid features with multiple local recurrences: report of a case with clinicopathologic and immunohistochemical studies.International journal of clinical and experimental pathology · 2025Article
- Morphological Features of the Spectrum of Ghost Cell Odontogenic Lesions.Head and neck pathology · 2024Article
- Imaging approach for jaw and maxillofacial bone tumors with updates from the 2022 World Health Organization classification.World journal of radiology · 2024Review
- Histopathological Insight of a Case of Adenoid Ameloblastoma: A Rare Odontogenic Tumor.Case reports in dentistry · 2024Article
- Demystifying Histologic Conundrum of Adenoid Ameloblastoma: Case Report with Literature Review.Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India · 2023Article
- Adenoid Ameloblastoma with BRAF p.V600E Mutation Revealing Ameloblastomatous Origin: A First Case Report.Head and neck pathology · 2023Article
- A Curious Case of Hybrid Ameloblastoma.Cureus · 2023Article
- [The new WHO classification of jaw tumours].Pathologie (Heidelberg, Germany) · 2023Review
- Proceedings of the 2023 North American Society of Head and Neck Pathology Companion Meeting, New Orleans, LA, March 12, 2023: Odontogenic Tumors: Have We Achieved an Evidence-Based Classification.Head and neck pathology · 2023Review
- Review
- Adenoid Ameloblastoma: The Histological Paradox.Head and neck pathology · 2022Article
- The World Health Organization Classification of Odontogenic Lesions: A Summary of the Changes of the 2022 (5th) Edition.Turk patoloji dergisi · 2022Review
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Authors and funding
5 authors at 2 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Adenoid ameloblastoma is a hybrid odontogenic tumour showing histopathological features of both ameloblastoma and adenomatoid odontogenic tumour (AOT), with approximately 40 cases reported in the literature. The aims of the report are to illustrate the diagnostic challenges of adenoid ameloblastoma using three new cases and to analyze evidence in literature to consider adenoid ameloblastoma as a new sub type of ameloblastoma. A literature review was performed with the key words-adenoid ameloblastoma, hybrid/composite odontogenic tumours, hybrid ameloblastoma and adenomatoid odontogenic tumour, ameloblastoma with inductive changes, dentinoid and dentinoma to select the cases compatible with the diagnosis of adenoid ameloblastoma. Out of the 40 cases reported in literature, 31 cases with sufficient information and 3 new cases were analyzed. Out of the 34 adenoid ameloblastomas majority of tumours (76.5%) occurred in adults with age ranging from 25 to 55 years. Slight female predilection with a male:female ratio of 0.9:1 was observed. Approximately, 64.7% occurred in the mandible. Radiologically, 82.4% of adenoid ameloblastomas presented as radiolucent lesions while 47.1% occurred with ill-defined margins and cortical perforation at diagnosis. Histopathologically, 70.8% of tumours presented as plexiform ameloblastomas, while duct like structures/glandular structures were the commonest feature supportive of adenomatoid odontogenic tumour observed in overwhelming majority of 95.9% of adenoid ameloblastomas. 91.6% of tumours showed inductive change in the form of dentinoid. Further, 45.4% of the tumours developed at least one recurrence following surgical excision. The report presents literature review based evidence to show the existence of adenoid ameloblastoma, which is demographically similar to conventional ameloblastoma but with histopathological differences and presenting with higher rate/multiple recurrences, indicating its biological aggressiveness. Thus, we would like to propose the inclusion of adenoid ameloblastoma as a sub type of ameloblastoma in the next revision of the WHO odontogenic tumour classification.
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