Yang Guang, Li Chenguang, Chen Xin, Liu Yaohua, Han Dayong, Gao Xin, Kawamoto Keiji, Zhao Shiguang
Department of Neurosurgery, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, P.R. China ; Institute of Brain Science, Harbin Medical University, Harbin, Heilongjiang, P.R. China.
Computer, Electrical and Mathematical Sciences and Engineering Division, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia.
Oncol Lett. 2014 Jul;8(1):183-186. doi: 10.3892/ol.2014.2143. Epub 2014 May 13.
The present study reports a rare case of large capillary hemangioma of the temporal bone with a dural tail sign. A 57-year-old female presented with pulsatile tinnitus and episodic vertigo associated with a ten-year history of an intermittent faint headache. Magnetic resonance imaging revealed a mass in the right petrous bone, which was hypointense on T1-weighted images and heterogeneously hyperintense on T2-weighted images, and showed a dural tail sign following gadolinium administration. Pre-operatively, this tumor was believed to be a meningioma. During surgery, the vascular tumor was removed by a modified pterional approach. A histopathological examination indicated that the tumor was a capillary hemangioma. Although intraosseous capillary hemangiomas are rare, they most frequently affect the temporal bone. Hemangiomas of the temporal bone may mimic other more common basal tumors. The diagnosis is most often made during surgical resection. The dural tail sign is not specific for meningioma, as it also occurs in other intracranial or extracranial tumors. The treatment of intratemporal hemangiomas is complete surgical excision, with radiotherapy used for unresectable lesions. To the best of our knowledge, the present study is the fourth case of intraosseous intracranial capillary hemangioma, but the largest intratemporal hemangioma to be reported in the literature to date.
本研究报告了一例罕见的颞骨大毛细血管瘤伴硬脑膜尾征病例。一名57岁女性,有搏动性耳鸣和发作性眩晕,伴有间歇性轻度头痛10年病史。磁共振成像显示右侧岩骨有一肿块,在T1加权图像上呈低信号,在T2加权图像上呈不均匀高信号,注射钆后显示硬脑膜尾征。术前,该肿瘤被认为是脑膜瘤。手术中,通过改良翼点入路切除了血管性肿瘤。组织病理学检查表明该肿瘤为毛细血管瘤。虽然骨内毛细血管瘤罕见,但最常累及颞骨。颞骨血管瘤可能类似其他更常见的颅底肿瘤。诊断大多在手术切除时做出。硬脑膜尾征并非脑膜瘤所特有,因为它也见于其他颅内或颅外肿瘤。颞骨内血管瘤的治疗是完整手术切除,不可切除的病变则采用放射治疗。据我们所知,本研究是第四例骨内颅内毛细血管瘤病例,但却是迄今为止文献报道中最大的颞骨内血管瘤。