Can I Diagnose a Vestibular Schwannoma Using Non-Contrast Imaging?

N. Yang
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Abstract

“I have an adult patient with new-onset unilateral sensorineural hearing loss. I would like to rule out a vestibular schwannoma by performing an MRI exam. However, the patient has a kidney problem that prevents him from receiving contrast material. Can I still diagnose a vestibular schwannoma using a non-contrast imaging study?” The answer to this question is ... YES! At the current time, gadolinium-enhanced T1-weighted magnetic resonance imaging (MRI) is considered the gold standard for the diagnosis of vestibular schwannomas.1 However, the use of gadolinium-based contrast material may be contraindicated in patients with impaired renal function, in those who have had an allergic reaction to such contrast material, and in patients who are or may be pregnant. High-resolution T2-weighted MR sequences as a means of visualizing the fluid-filled inner ear and the 7th and 8th cranial nerves in the internal auditory canal and cerebellopontine angle cistern was described in the early 1990’s.2 These steady-state imaging sequences currently include various manufacturer-specific sequences such as CISS (Constructive Interference into Steady State, Siemens), FIESTA-C (Fast Imaging Employing Steady-state Acquisition Cycled Phases, GE), DRIVE (Driven Equilibrium Radiofrequency Reset Pulse, Philips), bFFE (Balanced Fast Field Echo, Philips) and SPACE (Sampling Perfection with Application optimized Contrasts using different flip angle Evolutions, Siemens).3 The submillimeter-resolution images from these sequences can be manipulated on computer-based DICOM imaging software to provide reformatted images in non-orthogonal planes that allow visualization of the entire 8th cranial nerve, from the brainstem to the fundus of the internal auditory canal. In these sequences, cerebrospinal fluid (CSF) displays a high signal intensity that provides an excellent contrasting background to the inherent low signal intensity of the 7th and 8th cranial nerves. (Figure 1) Similar to the nerves, a vestibular schwannoma will appear as a low-intensity (dark) filling defect that may be nodular, oblong, or ice cream cone-shaped, and located in the internal auditory canal and/or the cerebellopontine angle cistern immediately adjacent to it. (Figure 2) In evaluating a patient for the presence of a vestibular schwannoma, the current medical literature indicates that high-resolution T2- weighted imaging sequences have a high sensitivity and specificity compared to gadolinium-enhanced T1-weighted imaging. However, T2-weighted imaging alone may not detect inflammatory, infectious or malignant conditions that may also present with sensorineural hearing loss.1 As such, a gadolinium-enhanced T1-weighted sequence will be needed when such conditions are suspected. Finally, local experience with institutions that perform imaging of the internal auditory canal and cerebellopontine angle shows that not all centers routinely perform the high-resolution T2-weighted imaging sequences. Therefore, it would be prudent to specifically indicate the need for “a T2-weighted imaging sequence with submillimeter- resolution, such as the CISS or FIESTA-C sequence” in the imaging request, in order to ensure the performance of the appropriate imaging strategy.
非对比成像能诊断前庭神经鞘瘤吗?
“我有一个新发单侧感音神经性听力损失的成年患者。我想通过核磁共振检查排除前庭神经鞘瘤的可能性。然而,患者的肾脏有问题,使他无法接受造影剂。我还能通过非对比成像研究来诊断前庭神经鞘瘤吗?”这个问题的答案是……是的!目前,钆增强t1加权磁共振成像(MRI)被认为是诊断前庭神经鞘瘤的金标准然而,肾功能受损的患者、对此类造影剂有过敏反应的患者以及怀孕或可能怀孕的患者可能忌用钆基造影剂。在20世纪90年代初,高分辨率t2加权MR序列作为一种显示充满液体的内耳、内耳道和桥小脑角池内的第7和第8脑神经的手段被描述这些稳态成像序列目前包括各种制造商特定的序列,如CISS(构建稳态干涉,西门子),fista - c(采用稳态采集循环相位的快速成像,GE), DRIVE(驱动平衡射频复位脉冲,飞利浦),bFFE(平衡快速场回波,飞利浦)和SPACE(使用不同翻转角度演化的应用优化对比的采样完美,西门子)来自这些序列的亚毫米分辨率图像可以在基于计算机的DICOM成像软件上进行操作,以提供非正交平面的重新格式化图像,从而使从脑干到内耳道底的整个第8脑神经可视化。在这些序列中,脑脊液(CSF)显示高信号强度,与第7和第8脑神经固有的低信号强度提供了极好的对比背景。(图1)与神经相似,前庭神经鞘瘤表现为低强度(深色)充盈缺损,可呈结节状、椭圆形或冰淇淋锥状,位于内耳道和/或紧邻的桥小脑角池。(图2)在评估患者是否存在前庭神经鞘瘤时,目前的医学文献表明,与钆增强t1加权成像相比,高分辨率T2加权成像序列具有更高的灵敏度和特异性。然而,单独的t2加权成像可能无法检测到炎症、感染性或恶性疾病,这些疾病也可能伴有感音神经性听力损失因此,当怀疑这种情况时,需要钆增强t1加权序列。最后,当地进行内耳道和桥小脑角成像的机构的经验表明,并非所有中心都常规进行高分辨率t2加权成像序列。因此,在成像请求中明确指出需要“亚毫米分辨率的t2加权成像序列,如CISS或fista - c序列”是谨慎的,以确保适当的成像策略的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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