High Prevalence of Dysplastic Development of Sacral Vertebral Arches in Pediatric Enuresis.

IF 1.8 3区 医学 Q3 UROLOGY & NEPHROLOGY
Hideo Ozawa, Takakuki Shibano, Isao Tanaka, Toshitaka Taniguchi, Michael B Chancellor, Naoki Yoshimura
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引用次数: 1

Abstract

Purpose: This is the first report to compare 3-dimensional computed tomography (3D-CT) images between pediatric patients with enuresis and children without lower urinary tract symptoms who underwent pelvic CT for other reasons.

Methods: Forty-seven children (33 boys and 14 girls) with primary enuresis underwent 3D-CT of sacrococcygeal bones. The control group consisted of 138 children (78 boys and 60 girls) who underwent pelvic CT for other reasons. First, we determined the presence or absence of unfused sacral arches at the L4-S3 levels in both cohorts. Subsequently, we compared the fusion of sacral arches in age- and sex-matched children from these 2 groups.

Results: Dysplastic sacral arches, characterized by lack of fusion at 1 or more levels of the S1-3 arches, were observed in nearly all patients in the enuresis group. In the control group (n=138), 54 of 79 children over 10 years old (68%) exhibited fused sacral arches at 3 S1-3 levels. All 11 control children under 4 years old displayed at least 2 unfused sacral arches at the S1-3 levels. In a comparative study of age- and sex-matched patients with enuresis and control children aged 5 to 13 years (n=32 for each group, with 21 boys and 11 girls; mean age, 8.0±2.2 years [range, 5-13 years]), only 1 patient (3%) in the enuresis group exhibited fusion of all S1-3 arches. In contrast, 20 of 32 control group participants (63%) had 3 fused sacral arches (P<0.0001).

Conclusion: Sacral vertebral arches typically fuse by the age of 10 years. However, in this study, children with enuresis exhibited a significantly elevated prevalence of unfused sacral arches, suggesting that dysplastic development of sacral vertebral arches may play a pathological role in enuresis.

Abstract Image

Abstract Image

小儿遗尿症患者骶椎弓发育不良的高发率。
目的:这是第一篇比较小儿遗尿症患者和无下尿路症状的儿童因其他原因行盆腔CT的三维计算机断层扫描(3D-CT)图像的报道。方法:47例原发性遗尿症患儿(男33例,女14例)行骶尾骨三维ct扫描。对照组包括138名儿童(78名男孩和60名女孩),他们因其他原因接受了盆腔CT检查。首先,我们确定两组患者在L4-S3水平是否存在未融合的骶弓。随后,我们比较了两组年龄和性别匹配儿童的骶弓融合情况。结果:在遗尿组几乎所有患者中都观察到发育不良的骶弓,其特征是S1-3弓的1个或多个节段缺乏融合。在对照组(n=138)中,79名10岁以上儿童中有54名(68%)在3个S1-3节段出现骶骨弓融合。所有11名4岁以下的对照儿童在S1-3节段至少有2个未融合的骶弓。在一项年龄和性别匹配的遗尿患者与5至13岁的对照组儿童的比较研究中(每组n=32,其中21名男孩和11名女孩;平均年龄8.0±2.2岁[范围,5-13岁]),遗尿组中仅有1例(3%)患者表现出全部S1-3弓融合。相比之下,32名对照组参与者中有20名(63%)有3个融合的骶椎弓(结论:骶椎弓通常在10岁时融合。然而,在本研究中,遗尿患儿表现出明显升高的未融合的骶椎弓患病率,提示骶椎弓发育不良可能在遗尿中起病理作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Neurourology Journal
International Neurourology Journal UROLOGY & NEPHROLOGY-
CiteScore
4.40
自引率
21.70%
发文量
41
审稿时长
4 weeks
期刊介绍: The International Neurourology Journal (Int Neurourol J, INJ) is a quarterly international journal that publishes high-quality research papers that provide the most significant and promising achievements in the fields of clinical neurourology and fundamental science. Specifically, fundamental science includes the most influential research papers from all fields of science and technology, revolutionizing what physicians and researchers practicing the art of neurourology worldwide know. Thus, we welcome valuable basic research articles to introduce cutting-edge translational research of fundamental sciences to clinical neurourology. In the editorials, urologists will present their perspectives on these articles. The original mission statement of the INJ was published on October 12, 1997. INJ provides authors a fast review of their work and makes a decision in an average of three to four weeks of receiving submissions. If accepted, articles are posted online in fully citable form. Supplementary issues will be published interim to quarterlies, as necessary, to fully allow berth to accept and publish relevant articles.
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