奥斯古德-施洛特病髌骨肌腱的超声弹性图表现

Anatomy Pub Date : 2022-04-20 DOI:10.2399/ana.21.9153256
M. Balaban, S. İkiz, I. Idilman
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引用次数: 0

摘要

目的:奥斯古德-谢尔特病有明确的超声表现。然而,该疾病的超声弹性图表现尚未明确。本研究的目的是评价奥斯古德-施拉特病(OSD)患者髌骨肌腱的b超(US)、彩色多普勒超声(CDUS)和超声弹性成像(SEL)的表现,并与健康人进行比较。方法:采用US、CDUS和SEL对12例OSD患者和10例健康人的36条髌骨肌腱进行评估。评估各组髌骨远端肌腱的厚度、回声、CDUS和SEL表现。结果:共纳入22例个体(男19例,女3例)和36条肌腱(急性OSD 9例,慢性OSD 7例,对照健康肌腱20例)。OSD患者的髌骨肌腱较健康志愿者厚(5.68±2.32 mm比3.42±0.55 mm),差异有统计学意义(p=0.001)。根据SEL评价,OSD患者的髌骨肌腱均为2型,而健康志愿者的髌骨肌腱均为1型(p<0.001)。结论:骨性OSD患者髌骨远端肌腱较健康志愿者更粗、更软。急性OSD患者在CDUS上的腱内和/或腱周血管增加。我们认为这些发现可能与OSD患者的肌腱退行性变有关,并可用于评估该疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sonoelastography findings of the patellar tendon in Osgood-Schlatter disease
Objectives: There are ultrasonographic findings defined in Osgood-Schlatter disease. However, sonoelastographic findings of the disease have not been previously defined. The aim of this study was to evaluate the B-mode ultrasonography (US), Color Doppler ultrasonography (CDUS), and sonoelastography (SEL) findings of the patellar tendon in patients with Osgood-Schlatter disease (OSD) and compare it with healthy individuals. Methods: A total of 36 patellar tendons were evaluated in 12 patients with OSD and 10 healthy individuals by US, CDUS, and SEL. Thickness, echogenicity, CDUS, and SEL findings of the distal patellar tendon in each group were evaluated. Results: A total of 22 individuals (19 males, 3 females) and 36 tendons (9 with acute OSD, 7 with chronic OSD and 20 control healthy tendons) were included in this study. The patellar tendons were statistically significantly thicker in OSD patients in comparison with healthy volunteers (5.68±2.32 mm versus 3.42±0.55 mm) (p=0.001). According to the SEL evaluation, all of the patellar tendons in patients with OSD were of type 2 in contrast with all of the patellar tendons in healthy volunteers were of type 1 (p<0.001). Conclusion: Distal patellar tendon in patients with OSD was thicker and softer in comparison with healthy volunteers. The intratendinous and/or peritendinous vascularity on CDUS was increased in patients with acute OSD. We suggest that these findings could be associated with tendon degeneration in OSD patients and can be useful in the evaluation of the disease.
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