先天性上斜肌麻痹患者的手术效果:临床诊断与放射学诊断的比较

Maryam Saatchi , Shervin Sharif Kashani , Anita Ebrahimpour , Motahereh Sadegi , Mohammadreza Akbari , Arash Mirmohammadsadegi , Babak Masoomian , Masoud Aghsaei Fard
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摘要

目的 上斜肌麻痹(SO)的诊断可通过检查放射学和临床特征来实现。尽管放射学方法和临床方法都很有用,但两者并不总是一致的。方法通过临床评估或放射成像诊断出SO麻痹后,根据临床测量和核磁共振成像结果将患者分为三组。第一组患者的临床测量结果和核磁共振成像结果一致,显示为SO麻痹;第二组患者的临床测量结果未经核磁共振成像证实。相反,第 3 组的测量结果不确定,但核磁共振扫描显示有萎缩迹象。患者接受了下斜(IO)肌切除术,同时进行或不进行对侧下直肌回缩术,并收集了下斜肌切除术前后的眼球偏斜情况。在三阶段测试均呈阳性的 35 名患者中,有 15 人的核磁共振成像结果未显示明显的肌肉萎缩。相比之下,在核磁共振成像扫描中显示肌肉萎缩的患者中,58.8%的患者在三步评估的所有步骤中均呈阳性结果。第一组和第三组患侧肌肉体积缩小,分别为 110.988 ± 42.49 mm³ 和 91.5 ± 56.8 mm³。第 2 组患侧肌肉体积为 184.1 ± 44.64 立方毫米。在接受 IO 肌肉切除术的三组 SO 麻痹眼患者中,原位眼球肥大均有所减轻,组间差异无统计学意义(P = 0.1)。接受 IO myectomy 切除术并伴有对侧下直肌后退的 5 位 SO 麻痹患者均被归入第 3 组,他们术后的眼球后凸明显减轻。
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Surgical outcomes in patients with congenital superior oblique palsy: A comparison between clinical and radiological diagnosis

Purpose

The diagnosis of superior oblique (SO) palsy can be achieved by examining the radiological and clinical characteristics. Despite their usefulness, the radiological and clinical methods are not always aligned to each other. The objective of this research is to analyze the surgical results of eyes with SO palsy, based on whether the diagnosis was made radiologically or clinically.

Design

A prospective study, conducted at a single tertiary hospital.

Methods

Following the diagnosis of SO palsy, either through clinical assessment or radiological imaging, the patients were categorized into three distinct groups according to their clinical measurements and MRI findings. Group 1 exhibited consistent clinical measurements and MRI findings indicating SO palsy, whereas Group 2 displayed clinical measurements without MRI confirmation. In contrast, Group 3 presented inconclusive measurements, but MRI scans revealed signs of atrophy. Patients underwent inferior oblique (IO) myectomy with and without contralateral inferior rectus recession and ocular deviation before and after myectomy were collected.

Results

The study included 49 patients with congenital unilateral SO palsy (average age: 30 years). Out of 35 patients who tested positive across all three stages of the test, 15 did not show notable muscle atrophy in their MRI findings. In contrast, among those who displayed muscle atrophy in their MRI scans, 58.8 % had positive outcomes in all steps of the three-step assessment. Group 1 and 3 displayed a reduced muscle volume measuring 110.988 ± 42.49 mm³ and 91.5 ± 56.8 mm³, respectively, on the affected side. Group 2 showcased a muscle volume of 184.1 ± 44.64 mm³ on the affected side. In all three groups with SO palsy eyes who underwent IO myectomy, there was a reduction in hypertropia in the primary position, with no statistically significant differences observed among the groups (P = 0.1). All five patients with SO palsy who underwent IO myectomy with contralateral inferior rectus recession were classified in group 3, and they exhibited a significant reduction in hypertropia postoperatively.

Conclusion

Comparable results can be attained through IO surgery in patients with SO palsy, regardless of whether they are diagnosed through clinical or radiological means.

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