Shin M S, McElvein R B, Reeves R C, Ho K J
Department of Radiology, School of Medicine, University of Alabama, Birmingham 35233.
J Comput Tomogr. 1988 Jan;12(1):57-60. doi: 10.1016/0149-936x(88)90032-x.
A rare case of solitary neurofibroma of the vagus nerve in the aortopulmonary window masquerading as a developmental cyst is reported. Its computed tomographic characteristics and magnetic resonance imaging are described and correlated with pathologic findings. Although the features of such imaging modalities are quite characteristic for a neurofibroma, its differentiation from "atypical" developmental cysts may be difficult.
报告了一例罕见的主动脉肺动脉窗迷走神经孤立性神经纤维瘤，其伪装成发育性囊肿。描述了其计算机断层扫描特征和磁共振成像，并与病理结果相关联。尽管这些成像方式的特征对神经纤维瘤来说颇具特异性，但其与“非典型”发育性囊肿的鉴别可能存在困难。
