Rare Case of Maxillary Ameloblastoma: A Challenging Entity

Maxillary ameloblastoma is a rare benign, locally aggressive extragnathic sinonasal tract epithelial odontogenic neoplasm that arises from remnants of odontogenic epithelium, the lining of odontogenic cysts, basal cells of the oral mucosa, rests of the dental lamina, or heterotopic embryonic organ epithelium. It has an unusual incidence of 0.5 cases per million person-years worldwide, with no gender predilection, and is most commonly found in individuals in their 6th to 7th decades of life. In the present case report, the authors presented a case of a 77-year-old male who presented with a history of right-sided nasal obstruction for 15 days. Anterior rhinoscopic examination revealed a soft-tissue nasal mass covering the entire nasal cavity, protruding as a nasal polyp, while posterior rhinoscopy examination was found to be normal. A Computed Tomography (CT) scan of the paranasal sinuses showed evidence of a soft-tissue density mass with internal hyperdensities noted in the right maxillary sinus. The patient underwent endoscopic medial maxillectomy, and gross examination revealed multiple grey-brown soft-tissue fragments with haemorrhagic areas. Microscopic analysis showed a neoplasm arranged in cords lined by columnar epithelial cells exhibiting reversal of polarity, with a central stellate reticulum. No bony fragments, atypical mitosis, or necrosis were identified. The diagnosis was established through histological analysis. Although maxillary ameloblastoma is a benign tumour, it requires aggressive treatment to prevent recurrence and local invasion. Early diagnosis using histopathological and radiological methods is crucial for optimal treatment planning and follow-up of the patient. The present case is presented due to its rarity and the diagnostic challenges it poses, including the lack of definite clinical presentation and radiological dilemmas. It also aimed to examine the key features of ameloblastoma in the maxillary region, emphasising their clinical, radiological and histological characteristics.

Authors

Publication Details

Journal
National Journal of Laboratory Medicine
Published
2025-04-01
DOI
https://doi.org/10.7860/njlm/2025/77583.2908
Primary Topic
Oral and Maxillofacial Pathology
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Rare Case of Maxillary Ameloblastoma: A Challenging Entity

Kavitha Swaminathan, Kavita Vani, Deepa Anumala, A. R. Nataraj et al.
National Journal of Laboratory Medicine
Oral and Maxillofacial Pathology
article

Rare Case of Maxillary Ameloblastoma: A Challenging Entity

Kavitha Swaminathan, Kavita Vani, Deepa Anumala, A. R. Nataraj, R Padmavathi
article en

Abstract

Maxillary ameloblastoma is a rare benign, locally aggressive extragnathic sinonasal tract epithelial odontogenic neoplasm that arises from remnants of odontogenic epithelium, the lining of odontogenic cysts, basal cells of the oral mucosa, rests of the dental lamina, or heterotopic embryonic organ epithelium. It has an unusual incidence of 0.5 cases per million person-years worldwide, with no gender predilection, and is most commonly found in individuals in their 6th to 7th decades of life. In the present case report, the authors presented a case of a 77-year-old male who presented with a history of right-sided nasal obstruction for 15 days. Anterior rhinoscopic examination revealed a soft-tissue nasal mass covering the entire nasal cavity, protruding as a nasal polyp, while posterior rhinoscopy examination was found to be normal. A Computed Tomography (CT) scan of the paranasal sinuses showed evidence of a soft-tissue density mass with internal hyperdensities noted in the right maxillary sinus. The patient underwent endoscopic medial maxillectomy, and gross examination revealed multiple grey-brown soft-tissue fragments with haemorrhagic areas. Microscopic analysis showed a neoplasm arranged in cords lined by columnar epithelial cells exhibiting reversal of polarity, with a central stellate reticulum. No bony fragments, atypical mitosis, or necrosis were identified. The diagnosis was established through histological analysis. Although maxillary ameloblastoma is a benign tumour, it requires aggressive treatment to prevent recurrence and local invasion. Early diagnosis using histopathological and radiological methods is crucial for optimal treatment planning and follow-up of the patient. The present case is presented due to its rarity and the diagnostic challenges it poses, including the lack of definite clinical presentation and radiological dilemmas. It also aimed to examine the key features of ameloblastoma in the maxillary region, emphasising their clinical, radiological and histological characteristics.

National Journal of Laboratory Medicine
Openalex Percentile: Top 89%
Oral and Maxillofacial Pathology
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.