AI Article Synopsis

  • The study focused on differentiating between ameloblastomas and central giant cell granulomas (CGCGs) using multidetector CT (MDCT) imaging, as no previous analyses had been conducted.
  • Researchers reviewed 12 CGCGs and 33 ameloblastomas, finding distinct features such as CGCGs being multilocular with hyperenhancement, while ameloblastomas were usually unilocular with less enhancement.
  • The analysis concluded that specific characteristics, particularly a multilocular structure with significant hyperenhancement in soft tissue and matrix mineralization, can help in accurately diagnosing CGCGs.

Article Abstract

Background: No qualitative or quantitative analysis of contrast-enhanced computed tomography (CT) images has been reported for the differentiation between ameloblastomas and central giant cell granulomas (CGCGs).

Aim: To describe differentiating multidetector CT (MDCT) features in CGCGs and ameloblastomas and to compare differences in enhancement of these lesions qualitatively and using histogram analysis.

Methods: MDCT of CGCGs and ameloblastomas was retrospectively reviewed to evaluate qualitative imaging descriptors. Histogram analysis was used to compare the extent of enhancement of the soft tissue. Fisher's exact tests and Mann-Whitney test were used for statistical analysis ( < 0.05).

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 mineralization 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 mineralization was present in 69.7% of cases. Quantitatively, the enhancement of soft tissue in CGCG was significantly higher than in ameloblastoma on histogram analysis ( < 0.05), with a minimum enhancement of > 49.05 HU in the tumour providing 100% sensitivity and 85% specificity in identifying a CGCG.

Conclusion: A multilocular, lytic sclerotic lesion with significant hyperenhancement in soft tissue, which spares the angle of the mandible and has matrix mineralization, should indicate prospective diagnosis of CGCG

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9521432PMC
http://dx.doi.org/10.4329/wjr.v14.i9.329DOI Listing

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