首页> 外文期刊>Journal of neurosurgery. >Multifocal cavernous hemangioma of the jugular foramen: a rare skull base vascular malformation
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Multifocal cavernous hemangioma of the jugular foramen: a rare skull base vascular malformation

机译:颈颈孢子型多灶性海绵状血管瘤:罕见的头骨基血管畸形

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摘要

Jugular foramen cavernous hemangiomas are extremely rare vascular malformations, and, to the best of the authors' knowledge, their occurrence as multifocal lesions involving both intra- and extracranial compartments has never been reported before. Here, the authors describe the case of a 60-year-old woman with a complex multifocal jugular foramen cavernous hemangioma. The patient presented with signs and symptoms concerning for jugular foramen syndrome, as well as a right neck mass. Surgical extirpation of the lesion was achieved by a multidisciplinary team via a right infratemporal fossa approach (Fisch type A) with concurrent high neck dissection and a closure buttressed with an autologous fat graft and a temporoparietal fascial flap. Although rare, cavernous hemangiomas should be included in the differential diagnosis of jugular foramen masses.
机译:颈神经孢子血管血管瘤是极其罕见的血管畸形,并且据作者的知识,他们以前从未报道过的涉及和颅外隔室的多焦点病变。 在这里,作者描述了一个60岁女性的案例,具有复杂的多焦点颈神经孢子血管瘤。 患者患有关于颈颈综合征的症状和症状,以及右颈部质量。 由多学科团队通过右颞型窝(FISCH A型)通过并发高颈部剖面和闭合,用自体脂肪移植和临时粉状襟翼和临时粉状襟翼,通过右颞型窝(FISCH A型)来实现病变的外科突出。 虽然罕见的血管瘤应该被列入颈颈孢子群的鉴别诊断。

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