Shi Zhenshan, Zhuang Qian, Cao Dairong
Department of Radiology, First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, PR China.
Department of Pharmacy, Union Hospital of Fujian Medical University, Fuzhou, Fujian, PR China.
Acta Radiol Open. 2015 Dec 12;4(12):2058460115608660. doi: 10.1177/2058460115608660. eCollection 2015 Dec.
We report an extremely rare case of intramastoid neurofibroma. A mass with destruction of the mastoid bone of a 51-year-old woman was examined with computed tomography. Subsequent magnetic resonance imaging demonstrated an ill-defined soft tissue mass with the opacification of mastoid air cells that had a mass effect in the same area. The patient underwent left subtotal temporal bone resection, and histological and immunohistochemical findings confirmed the lesion to be a neurofibroma. Given that similar imaging features of neurofibroma have been reported previously elsewhere in the head/neck and extremities, we suggest that it may be possible to include this tumor in the preoperative differential diagnosis.
我们报告了一例极其罕见的乳突内神经纤维瘤病例。对一名51岁女性乳突骨破坏的肿块进行了计算机断层扫描检查。随后的磁共振成像显示,乳突气房混浊,存在边界不清的软组织肿块,在同一区域有占位效应。患者接受了左侧颞骨次全切除术,组织学和免疫组化结果证实该病变为神经纤维瘤。鉴于此前在头颈部和四肢其他部位已报道过神经纤维瘤的类似影像学特征,我们建议在术前鉴别诊断中可能可以考虑这种肿瘤。