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Large capillary hemangioma of the temporal bone with a dural tail sign: A case report

机译:颞骨大毛细血管血管瘤伴硬脑膜尾征:1例

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摘要

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.
机译:本研究报告少见的颞骨大毛细血管血管瘤伴硬脑膜尾征。一位57岁的女性出现搏动性耳鸣和发作性眩晕,伴有间歇性微弱头痛的十年病史。磁共振成像显示右岩骨有一块肿块,在T1加权图像上呈低点,在T2加权图像上呈异质性超强,并在施用administration后出现硬脑膜尾征。术前,该肿瘤被认为是脑膜瘤。在手术过程中,通过改良的翼状动脉入路切除了血管肿瘤。组织病理学检查表明该肿瘤是毛细血管瘤。尽管骨内毛细血管瘤很少见,但它们最常影响颞骨。颞骨血管瘤可模仿其他更常见的基底肿瘤。诊断通常是在手术切除过程中做出的。硬脑膜尾征对脑膜瘤不是特异性的,因为它也出现在其他颅内或颅外肿瘤中。颞内血管瘤的治疗是完全手术切除,放疗用于无法切除的病变。据我们所知,本研究是骨内颅内毛细血管瘤的第四例,但迄今为止文献中报道的最大的颞内血管瘤。

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