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首页> 外文期刊>AJNR. American journal of neuroradiology >Pineocytoma mimicking a pineal cyst on imaging: true diagnostic dilemma or a case of incomplete imaging?
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Pineocytoma mimicking a pineal cyst on imaging: true diagnostic dilemma or a case of incomplete imaging?

机译:松果细胞瘤在影像学上模拟松果体囊肿:真正的诊断难题还是影像不完整?

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BACKGROUND AND PURPOSE: Pineocytomas have been described as well-circumscribed, homogeneously enhancing masses. However, there is considerable variability in this appearance, and certain pineocytomas may have a predominantly cystic appearance on imaging. This has led some to suggest that differentiation between pineocytomas and pineal cysts may not be possible. We have attempted to determine if cystic pineocytomas could be found in a series of these tumors evaluated by CT and MR imaging. MATERIALS AND METHODS: We searched the radiology literature as well as the medical records from our own institution for pathologically proved pineocytomas with available preoperative imaging or imaging reports, with specific focus on whether postcontrast MR imaging was included. In cases in which images were available, they were evaluated by a Certificate of Added Qualification (CAQ)-certified neuroradiologist and a radiology resident, who attempted to determine if the pineocytomas had any MR imaging characteristics oftypical pineal cysts. To be considered a typical pineal cyst, an area of signal-intensity abnormality must be centered on the pineal recess, demonstrating internal homogeneity on T2-weighted imaging, following CSF signal intensity on T1- and T2-weighted images, without any marginal lobularity or nodular contrast enhancement and a wall thickness of <2 mm. In cases in which imaging was not available, radiology reports and/or descriptions provided in the radiology literature were reviewed by a CAQ-certified neuroradiologist. For any lesion described as cystic, we again attempted to elucidate the exact extent of imaging that was performed, note specific lesion characteristics, and determine if the lesion met the criteria described previously. Finally, for tumors in which image size was provided, the mean value of maximal tumor dimension, SD, median, and range were calculated. RESULTS: Forty-four pathologically proved cases of pineocytomas from the radiology literature, as well as 8 pathologically proved cases of pineocytomas from our institution with available imaging studies and/or reports, were reviewed. Of these, 23 were solid masses, and 7 were partially solid and cystic, whereas 14 tumors could not be completely characterized due to incomplete imaging evaluation. Eight were primarily cystic; however, none of these could be confidently characterized as meeting the criteria for a typical cyst. CONCLUSION: In our analysis, no truly cystic pineocytomas were identified.
机译:背景和目的:松果细胞瘤已被描述为界限清楚,质量均一的肿块。但是,这种外观有相当大的可变性,某些松​​细胞瘤在成像时可能主要具有囊性外观。这导致一些人认为,可能无法区分皮细胞瘤和松果体囊肿。我们试图确定在通过CT和MR成像评估的一系列此类肿瘤中是否可以发现囊性皮细胞瘤。材料与方法:我们从放射治疗的文献资料以及我们机构的病历中检索了经病理证实的皮细胞瘤,并有术前影像学检查或影像学报告,特别侧重于是否包括造影后MR成像。在有图像的情况下,由具有附加资格证书(CAQ)的神经放射科医生和放射科住院医师对图像进行评估,他们试图确定松果细胞瘤是否具有典型的松果体囊肿的任何MR成像特征。要被认为是典型的松果体囊肿,信号强度异常区域必须以松果体凹处为中心,在T1和T2加权图像上的CSF信号强度之后,在T2加权成像上表现出内部均匀性,而没有任何边缘小叶或结节状对比度增强,壁厚<2 mm。如果无法获得影像,则由CAQ认证的神经放射科医生审查放射学报告和/或放射学文献中提供的描述。对于描述为囊性的任何病变,我们再次尝试阐明所进行成像的确切程度,注意特定的病变特征,并确定病变是否符合前述标准。最后,对于提供图像尺寸的肿瘤,计算最大肿瘤尺寸,SD,中位数和范围的平均值。结果:回顾了放射学文献中的44例经病理学证实的胞浆瘤病例,并回顾了本院已有影像学研究和/或报道的8例经病理学证实的胞浆瘤病例。其中,有23个为实性肿块,有7个为部分实性和囊性肿块,而14个肿瘤由于成像评估不完整而无法完全鉴定。八个主要是囊性的。然而,这些都不能确定地符合典型囊肿的标准。结论:在我们的分析中,没有发现真正的囊性松果细胞瘤。

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