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Oculomotor nerve: Clinical anatomy

机译:动眼神经:临床解剖

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In this article, we illustrate and briefly describe a medial approach, in the sagittally sectioned preserved human brain, to display the oculomotor nerve, in situ and in continuity. The method has been successfully used by Milanes-Rodriguez for several cohorts of our second-year medical students, and can be completed within a 90-min dissecting session. We also review the most common clinical manifestation of oculomotor disorder Introduction Despite congenital anomaly of oculomotor nerve is a rare condition some reports about oculomotor disorders due to nerve fenestration [1,2,3], abnormal course [4], hypoplasia in congenital fibrosis of the extraocular muscles [5,6,7], in Duane-Radial Ray Syndrome [8] in congenital extraocular muscle misinnervation [9], among others have been published [10,11,12,13,14]The third, fourth, and sixth cranial nerves innervate the extraocular muscles that position the globes in the orbits. Extraocular muscle paralysis resulting from destructive lesions in one or all of these cranial nerves results in failure of one or both eyes to rotate in concert with the other eye.CN III is the only cranial nerve with a subnuclear complex that arises in the dorsal mesencephalon at the level of the superior colliculus. Fascicles pass through the parenchyma of the midbrain via the red nucleus and corticospinal tract. They exit the mesencephalon and emerge into the subarachnoid space between the cerebral peduncles.The primary symptom is diplopia from misalignment of the visual axes, and the pattern of image separation is the key to diagnosing which particular cranial nerve (and extraocular muscle) is involved. With unilateral third cranial nerve palsy, the involved eye usually is deviated down and out (infraducted, abducted), and there is ptosis, which may be severe enough to cover the pupil. In addition, pupillary dilatation can cause symptomatic glare in bright light (if the ptotic lid does not cover the pupil), and paralysis of accommodation causes blurred vision for near objects [12,15,16,17,18].The oculomotor nerve arises from the anterior aspect of mesencephalon (midbrain). There are two nuclei for the oculomotor nerve: The oculomotor nucleus originates at the level of the superior colliculus. The muscles it controls are the ciliary muscle (affecting accommodation), and all extraocular muscles except for the superior oblique muscle and the lateral rectus muscle. The Edinger-Westphal nucleus supplies parasympathetic fibres to the eye via the ciliary ganglion, and thus controls pupil constriction. On emerging from the brain, the nerve is invested with a sheath of pia mater, and enclosed in a prolongation from the arachnoid.It passes between the superior cerebellar (below) and posterior cerebral arteries (above), and then pierces the dura mater in front of and lateral to the posterior clinoid process, passing between the free and attached borders of the tentorium cerebelli.It runs along the lateral wall of the cavernous sinus, above the other orbital nerves, receiving in its course one or two filaments from the cavernous plexus of the sympathetic, and a communicating branch from the ophthalmic division of the trigeminal.It then divides into two branches, which enter the orbit through the superior orbital fissure, between the two heads of the lateral rectus.Here the nerve is placed below the trochlear nerve and the frontal and lacrimal branches of the ophthalmic nerve, while the nasociliary nerve is placed between its two rami: superior branch of oculomotor nerve inferior branch of oculomotor nerve As mentioned before the oculomotor nerve or cranial nerve number III is one of the cranial nerve that together with the trochlear (IV) and abducent (VI) supplies the extra ocular muscles that position the globes in the orbital cavity. Extraocular muscles paralyses result in failure of one eye to rotate in concern with the other producing misalignment of the visual axis with the resulting diplopia as a primary symptom[19
机译:在本文中,我们说明并简要描述了一种矢状切面保存的人脑的内侧方法,该方法可以原位连续地显示动眼神经。 Milanes-Rodriguez已成功地将该方法用于我们的二年级医学生的多个队列,并且可以在90分钟的解剖过程中完成。我们还回顾了动眼障碍的最常见临床表现简介尽管先天性动眼神经异常是一种罕见病,但有关神经开窗[1,2,3],病程异常[4],先天性纤维化发育不全的一些有关动眼障碍的报道。先天性眼外肌神经支配[9]中的Duane-Radial Ray综合征[8]中的眼外肌[5,6,7]等[10,11,12,13,14]第三,第四,第六颅神经支配眼球,将眼球定位在眼眶中。其中一只或所有这些颅神经的破坏性病变导致眼外肌麻痹导致一只或两只眼睛无法与另一只眼睛协调旋转.CN III是唯一在下背部中脑出现的具有亚核复合物的颅神经上丘的水平。束通过红色核和皮质脊髓束穿过中脑薄壁组织。它们离开中脑并进入脑梗之间的蛛网膜下腔。主要症状是视轴未对准引起的复视,图像分离的模式是诊断涉及特定颅神经(和眼外肌)的关键。单侧第三颅神经麻痹时,受累眼通常向下和向外偏斜(偏斜,外展),并有上睑下垂,可能足以遮盖瞳孔。此外,瞳孔扩张会在强光下导致症状性眩光(如果眼睑盖未覆盖瞳孔),并且房颤麻痹会导致附近物体的视物模糊[12,15,16,17,18]。动眼神经出现从中脑(中脑)的前面看。动眼神经有两个核:动眼核起源于上丘的水平。它控制的肌肉是睫状肌(影响调节),以及除上斜肌和直肌外侧肌以外的所有眼外肌。爱丁格-威斯特法尔核通过睫状神经节向神经提供副交感纤维,从而控制瞳孔收缩。在从大脑出来时,神经被皮亚鞘覆盖,并被蛛网膜延长而封闭,它穿过小脑上侧(下)和大脑后动脉(上)之间,然后刺穿硬脑膜后斜突的前部和外侧,在小脑腱的自由边界和附着边界之间穿过,沿着海绵窦的侧壁,在其他眶神经上方延伸,在此过程中从海绵体中接收一两根细丝交感神经丛,从三叉神经的眼科分裂而来的是一个连通分支,然后分成两个分支,通过上眼眶裂孔进入外侧直肌的两个头之间的轨道,这里的神经被置于滑车神经和眼神经的额,泪分支,而鼻睫状神经位于其两个分支之间:动眼神经的上分支,下分支o动眼神经如前所述,眼动神经或颅神经是颅神经之一,与滑车(IV)和外展肌(VI)一起提供了将眼球定位在眼眶内的眼外肌。眼外肌麻痹导致一只眼睛无法旋转,而另一只眼睛旋转则导致视轴错位,从而导致复视为主要症状[19]。

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