Sayama Christina M, MacDonald Joel D
Department of Neurosurgery, University of Utah, Salt Lake City, UT 84132, USA.
Pediatr Neurosurg. 2010;46(4):308-12. doi: 10.1159/000322016. Epub 2010 Dec 30.
Aneurysmal bone cysts (ABC) were originally described by Jaffe and Lichtenstein [Arch Surg 1942;44:1004-1025] in 1942 as nonneoplastic benign lesions with obscure pathogenesis. ABC occurring in the temporal bone are uncommon. Those arising from the petrous portion of the temporal bone are exceedingly rare. We report a right petrous ABC in a 16-year-old girl who presented clinically with hearing loss, facial weakness, and facial numbness and tingling. Her symptoms were preceded by a coincidental traumatic concussion 4 months earlier. Preoperative magnetic resonance imaging and computed tomography findings were both consistent with an ABC, although the lesion was noted to be in a very unusual location. Surgical resection was performed with adjuvant preoperative embolization. The patient recovered complete facial sensation and movement, and follow-up imaging documented complete resection.
动脉瘤样骨囊肿(ABC)最初由贾菲和利希滕斯坦于1942年描述为发病机制不明的非肿瘤性良性病变。发生于颞骨的ABC并不常见。起源于颞骨岩部的则极为罕见。我们报告一例16岁女孩的右侧岩部ABC,其临床症状为听力丧失、面部无力以及面部麻木和刺痛感。4个月前她曾意外遭受脑震荡,之后出现了这些症状。术前磁共振成像和计算机断层扫描结果均与ABC相符,尽管该病变位于一个非常不寻常的位置。手术切除前进行了辅助性栓塞。患者面部感觉和运动功能完全恢复,随访影像学检查证实病变已完全切除。