Uglietta J P, Boyko O B, Rippe D J, Fuller G N, Schiff S J, Heinz E R
Department of Radiology, Duke University Medical Center, Durham, NC 27710.
J Comput Assist Tomogr. 1989 Nov-Dec;13(6):1061-4. doi: 10.1097/00004728-198911000-00021.
We report on a 46-year-old man with a congenital nasal dermoid cyst that extended intracranially to form large bifrontal intraaxial dermoid cysts, which became secondarily infected through a nasal dermal sinus tract. Computed tomography demonstrated bilateral frontal lobe ring enhancing cystic masses containing fat-fluid levels consistent with dermoid cyst abscesses. Axial and coronal CT of the skull base and nose demonstrated a midline bony canal extending from two dimples on the dorsum of the patient's nose to the base of the anterior cranial fossa. The clinical, CT, and surgical findings are reviewed as well as the embryogenesis of congenital nasal dermoid cysts.
我们报告了一名46岁男性,患有先天性鼻皮样囊肿,该囊肿向颅内延伸形成巨大的双侧额叶轴内皮样囊肿,并通过鼻皮窦道继发感染。计算机断层扫描显示双侧额叶环形强化囊性肿块,内含脂肪-液平面,符合皮样囊肿脓肿表现。颅底和鼻部的轴向及冠状位CT显示一条中线骨性管道,从患者鼻背部的两个凹陷延伸至前颅窝底部。本文回顾了临床、CT及手术 findings 以及先天性鼻皮样囊肿的胚胎发生。 (注:原文中“findings”未翻译,可能是笔误,正常应完整翻译,因未明确要求对其进行处理,故保留原文形式。)