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原发性眼眶脑膜瘤:41例患者的放射学研究综述

Primary orbital meningioma: a review of 41 patients investigated radiologically.

作者信息

Lloyd G A

出版信息

Clin Radiol. 1982 Mar;33(2):181-7. doi: 10.1016/s0009-9260(82)80057-3.

Abstract

The X-ray features in 41 patients with histologically verified primary meningiomas in the orbit are reviewed. These tumours arise from the sheath of the optic nerve (78%) or extradurally within the orbit, remote from the nerve (22%). Sheath meningiomas occur predominantly in middle-aged women. Characteristically they give little sign of their presence on plain X-rays, but may show minor variations in the size of the optic canal (22%) or calcification in the tumour (12.5%). The radiological diagnosis is based upon the computed tomography (CT) findings. Visual deterioration in a middle-aged or elderly patient with obvious optic nerve enlargement on CT and minimal or no enlargement of the optic canal is virtually diagnostic of a sheath meningioma. Primary extradural meningiomas in the orbit usually present with proptosis before compressing the optic nerve. The majority of these show some plain X-ray evidence of their presence such as localised or generalised orbital enlargement, hyperostosis of the orbital walls, or changes in the adjacent sinuses. In this group the tumour may be located inside or outside the rectus muscle cone and the CT changes are usually non-specific.

摘要

回顾了41例经组织学证实的眼眶原发性脑膜瘤患者的X线特征。这些肿瘤起源于视神经鞘(78%)或眼眶硬膜外、远离神经的部位(22%)。鞘膜脑膜瘤主要发生于中年女性。其特征是在普通X线片上几乎没有显示存在的迹象,但可能显示视神经管大小有轻微变化(22%)或肿瘤内钙化(12.5%)。放射学诊断基于计算机断层扫描(CT)结果。对于中老年患者,若CT显示视神经明显增粗而视神经管增粗轻微或无增粗,同时伴有视力减退,则几乎可诊断为鞘膜脑膜瘤。眼眶原发性硬膜外脑膜瘤在压迫视神经之前通常先出现眼球突出。其中大多数在普通X线片上有一些显示存在的证据,如局限性或普遍性眼眶扩大、眶壁骨质增生或相邻鼻窦改变。在这一组中,肿瘤可位于直肌圆锥内或外,CT改变通常不具有特异性。

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