Kim Seung-Hyun, Yi Sung-Tae, Cho Yoonae A, Uhm Chang-Sub
Department of Ophthalmology, Korea University College of Medicine, Seoul, South Korea.
Acta Ophthalmol Scand. 2006 Apr;84(2):182-7. doi: 10.1111/j.1600-0420.2005.00556.x.
To investigate the ultrastructures of tendon axonal profiles in infantile and intermittent exotropia. Tendon axonal profiles are composed of myotendinous nerve endings that are presumed to serve as sensorial receptors in ocular proprioception.
The study subjects included 10 patients with exotropia who had undergone surgery in one eye (recession and resection). They were divided into two equal groups. Five patients with infantile exotropia that had developed at under 12 months of age were allocated to group A. Another five, with intermittent exotropia that had developed at over 12 months of age, were allocated to group B. In all patients, medial recti were resected by 3-4 mm in order to obtain tissue samples, which were then examined under an electron microscope.
In group A, we noted many axonal degenerative findings, such as the retraction of axons from myelin sheaths with considerable shrinkage, axonal disintegration, and Schwann cell proliferation. On the other hand, we identified three unique findings in group B: intact axons with incomplete Schwann cell wrapping; intact Schwann cells not associated with axons, and disorganized Schwann cells with shrunken axons.
Different patterns of tendon axonal profiles were seen in association with the two types of exotropia. These differences may be related to the pathogenesis of these exotropia types.
研究婴儿型和间歇性外斜视中肌腱轴突轮廓的超微结构。肌腱轴突轮廓由肌-腱神经末梢组成,推测其在眼本体感觉中起感觉受体的作用。
研究对象包括10例单眼接受过手术(后徙和切除)的外斜视患者。他们被分为两组,每组5例。5例12个月龄以下发病的婴儿型外斜视患者被分配到A组。另外5例12个月龄以上发病的间歇性外斜视患者被分配到B组。所有患者均切除3-4mm内直肌以获取组织样本,然后在电子显微镜下进行检查。
在A组中,我们观察到许多轴突退变表现,如轴突从髓鞘中回缩并伴有明显萎缩、轴突崩解和雪旺细胞增殖。另一方面,我们在B组中发现了三个独特的表现:轴突完整但雪旺细胞包裹不完全;雪旺细胞完整但与轴突不相关;雪旺细胞紊乱且轴突萎缩。
在两种类型的外斜视中观察到肌腱轴突轮廓的不同模式。这些差异可能与这些类型外斜视的发病机制有关。