对比增强多检测器计算机断层扫描特征和直方图分析可以区分成釉细胞瘤和中央巨细胞肉芽肿。

IF 1.4 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Adarsh Ghosh, Meyyappan Lakshmanan, Smita Manchanda, Ashu Seith Bhalla, Prem Kumar, Ongkila Bhutia, Asit Ranjan Mridha
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引用次数: 0

摘要

背景:对比增强计算机断层扫描(CT)图像尚未报道成釉细胞瘤和中央巨细胞肉芽肿(cgcg)鉴别的定性或定量分析。目的:描述cgcggs和成釉细胞瘤的多探头CT (MDCT)特征的鉴别,并利用直方图分析比较这两种病变在增强上的定性差异。方法:回顾性分析cgcggs和成釉细胞瘤的MDCT表现,评价其定性影像学描述。采用直方图分析比较软组织增强程度。采用Fisher精确检验和Mann-Whitney U检验进行统计学分析(P < 0.05)。结果:回顾了12例cgcg和33例成釉细胞瘤。成釉细胞瘤倾向于后下颌,没有任何ccggs涉及角度。cgcg多房性(58.3%),混合溶性硬化(75%)。91%的cgcg中存在软组织成分,50%的cgcg表现为高增强(与周围肌肉相比),其余cgcg表现为等增强。83.3%的病例存在基质矿化。成釉细胞瘤表现为单眼(66.7%),溶解性(60.6%)肿块,81.8%的病例存在固体成分。63%的固相成分表现为等增强。69.7%的病例无基质矿化。定量地,在直方图分析中,CGCG中软组织的增强显著高于成膜细胞瘤(P < 0.05),肿瘤中最小增强> 49.05 HU,提供了100%的敏感性和85%的特异性来识别CGCG。结论:多室、溶解性硬化病变伴明显的软组织高强化,保留下颌骨的角度并有基质矿化,应提示CGCG的前瞻性诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Contrast-enhanced multidetector computed tomography features and histogram analysis can differentiate ameloblastomas from central giant cell granulomas.

Contrast-enhanced multidetector computed tomography features and histogram analysis can differentiate ameloblastomas from central giant cell granulomas.

Contrast-enhanced multidetector computed tomography features and histogram analysis can differentiate ameloblastomas from central giant cell granulomas.

Contrast-enhanced multidetector computed tomography features and histogram analysis can differentiate ameloblastomas from central giant cell granulomas.

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 U test were used for statistical analysis (P < 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 (P < 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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来源期刊
World journal of radiology
World journal of radiology RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
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