Klimo Paul, Jha Tushar, Choudhri Asim F, Joyner Royce, Michael L Madison
Murphey Neurologic & Spine Institute, Semmes, Memphis, Tennessee, United States ; Le Bonheur Children's Hospital, Memphis, Tennessee, United States ; Department of Neurosurgery, University of Tennessee Health Science Center, Memphis, Tennessee, United States ; St. Jude Children's Research Hospital, Memphis, Tennessee, United States.
J Neurol Surg Rep. 2013 Dec;74(2):105-10. doi: 10.1055/s-0033-1351115. Epub 2013 Jul 30.
Purpose Fibromyxomas and myxomas are benign tumors of mesenchymal origin usually found outside the nervous system, most commonly in the atrium of the heart. They can also arise in the mandible or maxilla, but it is exceedingly rare to find them within the skull base. The history, histologic features, and the literature, with emphasis on other pediatric cases, are reviewed for this uncommon skull base neoplasm. Methods We describe the case of a 13-year-old girl who presented with a 1-year history of facial weakness, numbness, and hearing loss. A large locally destructive tumor centered in the petrous bone was found on magnetic resonance imaging. Results A mastoidectomy combined with a middle fossa craniotomy was performed for gross total resection. The child is disease free 12 months after surgery. Conclusion Diagnosis could not be made solely on radiographic studies because of the lack of pathognomonic imaging features. Radical resection provided the patient the best chance of cure. Long-term surveillance is necessary to monitor for tumor recurrence.
纤维黏液瘤和黏液瘤是间叶组织起源的良性肿瘤,通常见于神经系统以外,最常见于心脏心房。它们也可发生于下颌骨或上颌骨,但在颅底发现极为罕见。本文回顾了这一罕见的颅底肿瘤的病史、组织学特征及相关文献,重点关注其他儿科病例。方法:我们描述了一名13岁女孩的病例,她有1年面部无力、麻木和听力丧失的病史。磁共振成像发现一个以岩骨为中心的巨大局部侵袭性肿瘤。结果:行乳突切除术联合中颅窝开颅术以实现肿瘤全切。患儿术后12个月无疾病复发。结论:由于缺乏特征性影像学表现,仅靠影像学检查无法确诊。根治性切除为患者提供了最佳治愈机会。需要长期监测以监测肿瘤复发。