Department of Paediatric Surgery, KK Women's & Children's Hospital, Singapore 229899, Singapore.
J Pediatr Surg. 2012 Dec;47(12):2273-8. doi: 10.1016/j.jpedsurg.2012.09.017.
We evaluated the incidence of congenital anomalies associated with anorectal malformations (ARMs) in relation to the anatomic type of ARM as defined by the Krickenbeck classification.
We reviewed 99 children with ARM in our institution from 2002 to 2011. Data were collected on patient demographics, type of ARM, and associated congenital anomalies, which were categorized according to organ systems. Statistical analysis was performed for comparison between groups using 'perineal fistula' as the base group.
There were 62 (63%) male patients. The majority had perineal fistulas (35, 35%). Seventy-seven (78%) had at least one associated malformation. The most frequent malformations seen were genitourinary (28, 28%) and spinal anomalies (26, 26%). Those with rectovesical fistula had the highest proportion of genitourinary malformations (Odds Ratio [OR], 41.3; 95% confidence interval [CI], 4.7-363.4). Those with cloaca (OR, 49.5; 95% CI, 3.4-718.9) and those with rectovestibular fistula (OR, 12.4; 95% CI, 2.3-65.6) were most likely to have major spinal abnormalities, with tethered cord seen in all groups. The rectovestibular group was also most likely to have other associated malformations (OR, 8.6; 95% CI, 2.2-32.8).
More than 75% of children with anorectal malformation have other associated malformations. Genitourinary anomalies are the most common. Major spinal anomalies are seen in all groups, affecting nearly half of those with rectovestibular fistula and those without fistula. The incidence of associated malformations in the rectovestibular group is higher than described in the literature. Thorough systematic evaluation of all infants with ARM should be done regardless of type of ARM.
我们评估了与 Krickenbeck 分类定义的肛门直肠畸形(ARM)解剖类型相关的先天性异常的发生率。
我们回顾了 2002 年至 2011 年在我院就诊的 99 例 ARM 患儿。收集患者人口统计学、ARM 类型和相关先天性异常的数据,根据器官系统进行分类。使用“会阴瘘”作为基础组,对组间进行统计分析比较。
62 例(63%)为男性患者。多数为会阴瘘(35 例,35%)。77 例(78%)至少有一种相关畸形。最常见的畸形是泌尿生殖系统(28 例,28%)和脊柱异常(26 例,26%)。那些有直肠膀胱瘘的患者泌尿生殖系统畸形的比例最高(优势比[OR],41.3;95%置信区间[CI],4.7-363.4)。那些有泄殖腔(OR,49.5;95% CI,3.4-718.9)和直肠前庭瘘(OR,12.4;95% CI,2.3-65.6)的患者最有可能出现严重的脊柱异常,所有组均可见脊髓栓系。直肠前庭组也最有可能出现其他相关畸形(OR,8.6;95% CI,2.2-32.8)。
超过 75%的肛门直肠畸形患儿有其他相关畸形。泌尿生殖系统异常最常见。所有组均可见严重的脊柱异常,几乎一半的直肠前庭瘘和无瘘患儿均有脊柱异常。直肠前庭组的相关畸形发生率高于文献报道。无论 ARM 类型如何,都应彻底系统地评估所有 ARM 患儿。