Ozawa Hideo, Shibano Takakuki, Tanaka Isao, Taniguchi Toshitaka, Chancellor Michael B, Yoshimura Naoki
Department of Urology, Mizushima Central Hospital, Kurashiki, Japan.
Department of Pediatrics, Mizushima Central Hospital, Kurashiki, Japan.
Int Neurourol J. 2023 Jun;27(2):124-128. doi: 10.5213/inj.2346024.012. Epub 2023 Jun 30.
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.
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.
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).
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.
本研究首次比较了遗尿症患儿与因其他原因接受盆腔CT检查的无下尿路症状儿童的三维计算机断层扫描(3D-CT)图像。
47例原发性遗尿症患儿(33例男孩,14例女孩)接受了骶尾骨的3D-CT检查。对照组由138例因其他原因接受盆腔CT检查的儿童(78例男孩,60例女孩)组成。首先,我们确定了两组中L4-S3水平未融合骶椎弓的存在与否。随后,我们比较了这两组年龄和性别匹配儿童的骶椎弓融合情况。
遗尿症组几乎所有患者均观察到发育异常的骶椎弓,其特征为S1-3椎弓的一个或多个水平缺乏融合。在对照组(n = 138)中,79例10岁以上儿童中有54例(68%)在S1-3的3个水平表现为骶椎弓融合。所有11例4岁以下的对照儿童在S1-3水平至少有2个未融合的骶椎弓。在年龄和性别匹配的遗尿症患者与5至13岁对照儿童(每组n = 32,其中21例男孩,11例女孩;平均年龄8.0±2.2岁[范围5-13岁])的比较研究中,遗尿症组仅有1例患者(3%)表现为S1-3所有椎弓融合。相比之下,对照组32例参与者中有20例(63%)有3个融合的骶椎弓(P<0.0001)。
骶椎弓通常在10岁时融合。然而,在本研究中,遗尿症患儿未融合骶椎弓的患病率显著升高,提示骶椎弓发育异常可能在遗尿症中起病理作用。