首页> 外文期刊>The Canadian Journal of Neurological Sciences: le Journal Canadien des Sciences Neurologiques >A Child with Intra-orbital Oculomotor Nerve Schwannoma without Neurofibromatosis
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A Child with Intra-orbital Oculomotor Nerve Schwannoma without Neurofibromatosis

机译:一例眼眶动眼神经神经鞘瘤而无神经纤维瘤病的儿童

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摘要

Orbital tumors constitute a heterogeneous array of lesions and pose numerous challenges in terms of diagnosis, imaging and treatment. The bony orbit contains an extremely complicated anatomical architecture composed of II, III, IV, VI cranial nerves, vessels, extra ocular muscles and the globe. Schwannoma of cranial nerves represent less than 8% of all intracranial neoplasms usually arising from the vestibulocochlear nerve. These tumors are commonly seen in association, with Neurofibromatosis and constitute approximately 1% of all orbital tumors. To date there are only 38 reported cases of orbital tumors arising from the oculomotor nerve, and only four arising within the orbit.
机译:眼眶肿瘤构成病变的异质性阵列,并且在诊断,成像和治疗方面提出了许多挑战。骨轨道包含一个非常复杂的解剖结构,该结构由II,III,IV,VI颅神经,血管,眼外肌和球体组成。在所有颅内肿瘤中,通常由前庭耳蜗神经引起的颅神经神经鞘瘤占不到8%。这些肿瘤通常与神经纤维瘤病有关,约占所有眼眶肿瘤的1%。迄今为止,仅报道了38例由动眼神经引起的眼眶肿瘤病例,而在眼眶内仅发生了4例。

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