Retrospective Study
Copyright ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Radiol. Sep 28, 2022; 14(9): 329-341
Published online Sep 28, 2022. doi: 10.4329/wjr.v14.i9.329
Contrast-enhanced multidetector computed tomography features and histogram analysis can differentiate ameloblastomas from central giant cell granulomas
Adarsh Ghosh, Meyyappan Lakshmanan, Smita Manchanda, Ashu Seith Bhalla, Prem Kumar, Ongkila Bhutia, Asit Ranjan Mridha
Adarsh Ghosh, Department of Radiology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, United States
Meyyappan Lakshmanan, Smita Manchanda, Department of Radiology, All India Institute of Medical Sciences, New Delhi 110029, India
Ashu Seith Bhalla, Department of Radiodiagnosis, All India Institute of Medical Sciences, New Delhi 110029, India
Prem Kumar, Ongkila Bhutia, Department of Oral & Maxillofacial Surgery, All India Institute of Medical Sciences, New Delhi 110029, India
Asit Ranjan Mridha, Department of Pathology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi 110029, India
Author contributions: Ghosh A contributed to methodology, software; Ghosh A and Lakshmanan M contributed to writing - original draft; Lakshmanan M contributed to investigation; Bhalla AS and Manchanda S contributed to conceptualization; Bhalla AS, Manchanda S, Kumar P, Bhutia O, and Mridha AR contributed to writing - review & editing, supervision; Kumar P, Bhutia O, and Mridha AR contributed to resources.
Institutional review board statement: The study was reviewed and approved by the All India Institute of Medical Science, New Delhi Institutional Review Board [(Approval No.IEC-622/03.07.2020, RP-31/2020)].
Informed consent statement: The requirement of signed consent forms was waived by the Institutional Ethics Board.
Conflict-of-interest statement: All the authors declare that they have no conflict of interest.
Data sharing statement: No additional data are available.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Ashu Seith Bhalla, MD, Professor, Department of Radiodiagnosis, All India Institute of Medical Sciences, New Delhi 110029, India. ashubhalla1@yahoo.com
Received: March 19, 2022
Peer-review started: March 19, 2022
First decision: June 16, 2022
Revised: July 5, 2022
Accepted: September 2, 2022
Article in press: September 2, 2022
Published online: September 28, 2022
ARTICLE HIGHLIGHTS
Research background

Contrast-enhanced multidetector computed tomography (MDCT) can provide unique information about ameloblastomas and central giant cell granulomas (CGCGs).

Research motivation

To evaluate contrast-enhanced multidetector computed tomography (MDCT) features of ameloblastomas and CGCGs.

Research objectives

To describe differentiating MDCT features in CGCGs and ameloblastomas and to compare the differences in the enhancement of these two lesions qualitatively and using histogram analysis.

Research methods

MDCTs of CGCGs and ameloblastomas were retrospectively reviewed to evaluate qualitative imaging descriptors. Histogram analysis was used to compare the extent of enhancement of the soft tissue. Fisher’s exact test and Mann–Whitney U test were used for statistical analysis (P < 0.05).

Research results

Twelve CGCGs and 33 ameloblastomas were reviewed. Ameloblastomas had a predilection for the posterior mandible with none of the CGCGs involving the angle. CGCGs were multilocular (58.3%), with a mixed lytic sclerotic appearance (75%). Soft tissue component was present in 91% of CGCGs, which showed hyperenhancement (compared to surrounding muscles) in 50% of cases, while the remaining showed isoenhancement. Matrix mineralisation was present in 83.3% of cases. Ameloblastomas presented as a unilocular (66.7%), lytic (60.6%) masses with solid components present in 81.8% of cases. However, the solid component showed isoenhancement in 63%. No matrix mineralisation was present in 69.7% of cases. Quantitatively, the enhancement of soft tissue in CGCGs was significantly higher than in ameloblastomas on histogram analysis (P < 0.05), with a minimum enhancement of > 49.05 HU in the tumour, providing 100% sensitivity and 85% specificity in identifying CGCG.

Research conclusions

A multilocular, lytic sclerotic lesion with significant hyperenhancing soft tissue component, which spares the angle of the mandible and has matrix mineralisation, should indicate a prospective diagnosis of CGCG.

Research perspectives

Future studies can evaluate the role of perfusion imaging for differentiating these two tumour types.