Liu Jun-Hua, Qi Meng, Sha Yan, Zhang Fang
Department of Radiology, Eye and ENT Hospital, Fudan University, Shanghai, China.
Curr Med Imaging. 2023 Mar 28. doi: 10.2174/1573405620666230328090514.
Chondrosarcoma in the mastoid is extremely rare, and it is easily misdiagnosed as a facial nerve schwannoma.
To identify and compare computed tomography (CT) and magnetic resonance imaging (MRI) features of chondrosarcoma in the mastoid involving the facial nerve, including diffusion-weighted MRI characteristics, with those of facial nerve schwannoma.
CT and MRI features of 11 chondrosarcomas in the mastoid involving the facial nerve and 15 facial nerve schwannomas, confirmed by histopathology, were retrospectively reviewed. The tumor location, size, morphological features, bone change, calcification, signal intensity, texture, enhancement characteristics, the extent of lesions, and apparent diffusion coefficients (ADCs) were evaluated.
On CT imaging, calcification could be found in 81.8% of chondrosarcomas (9/11) and 33.3% of facial nerve schwannomas (5/15). Chondrosarcoma in the mastoid appeared significantly hyperintense on T2-weighted images (T2WI) with low signal intensity septa in eight patients (72.7%, 8/11). After contrast, all chondrosarcomas showed inhomogeneous enhancement, and septal and peripheral enhancement could be found in six cases (54.5%, 6/11). Facial nerve schwannoma demonstrated inhomogeneous hyperintensity on T2WI in 12 cases (80%, 12/15), with obvious hyperintense cystic changes in seven cases. There were significant differences in calcification (P=0.014), T2 signal intensity (P=0.006), and septal and peripheral enhancement (P=0.001) between chondrosarcomas and facial nerve schwannomas. The ADCs of chondrosarcoma were significantly higher than those of facial nerve schwannomas (P<0.001).
CT and MRI with ADCs had the potential to improve the diagnostic accuracy of chondrosarcoma in the mastoid involving the facial nerve.
乳突部软骨肉瘤极为罕见,且极易被误诊为面神经鞘瘤。
识别并比较累及面神经的乳突部软骨肉瘤的计算机断层扫描(CT)和磁共振成像(MRI)特征,包括弥散加权MRI特征,与面神经鞘瘤的特征。
回顾性分析经组织病理学证实的11例累及面神经的乳突部软骨肉瘤和15例面神经鞘瘤的CT和MRI特征。评估肿瘤的位置、大小、形态特征、骨质改变、钙化、信号强度、质地、强化特征、病变范围及表观扩散系数(ADC)。
在CT成像上,81.8%(9/11)的软骨肉瘤和33.3%(5/15)的面神经鞘瘤可见钙化。8例(72.7%,8/11)乳突部软骨肉瘤在T2加权像(T2WI)上呈明显高信号,伴有低信号分隔。增强后,所有软骨肉瘤均表现为不均匀强化,6例(54.5%,6/11)可见分隔及周边强化。12例(80%,12/15)面神经鞘瘤在T2WI上呈不均匀高信号,7例有明显的高信号囊性改变。软骨肉瘤与面神经鞘瘤在钙化(P=0.014)、T2信号强度(P=0.006)及分隔和周边强化(P=0.001)方面存在显著差异。软骨肉瘤的ADC值显著高于面神经鞘瘤(P<0.001)。
CT、MRI及ADC值有助于提高累及面神经的乳突部软骨肉瘤的诊断准确性。