Department of Pediatric Surgery, Başkent University, Faculty of Medicine, Ankara/Turkey.
J Pediatr Surg. 2013 May;48(5):E37-43. doi: 10.1016/j.jpedsurg.2013.03.068.
There are case reports of duplication of the colon, rectum, anus, urinary system, lower genital tract, and external genitalia, spinal anomalies, and abdominal wall defects. However, it is rare to encounter a single newborn with all of the mentioned abnormalities, which have been defined as the caudal duplication syndrome (CDS). Herein, we present a newborn with an omphalocele, duplex external genitalia (with duplex labia minora and labia majora), duplex urethral orifices, duplex vaginal orifices, and duplex anal dimple with imperforate anus and rectovestibular fistula on both sides. Exploration revealed duplex appendix, colon duplication, duplex uterus (continuing with tuba and ovaries on both sides), duplex rectum, malrotation of the intestines, with the cecum located in the middle of the abdomen, defect in the intestinal mesentery, and internal herniation of the small intestines through this defect. The intestines were operatively reduced and the defect repaired.
已有结肠、直肠、肛门、泌尿系统、下生殖道和外生殖器、脊柱异常和腹壁缺陷重复的病例报告。然而,很少遇到一个新生儿同时存在上述所有异常,这些异常已被定义为尾部重复综合征(CDS)。在此,我们介绍了一例脐膨出患儿,表现为外生殖器双重(小阴唇和大阴唇双重)、尿道双重开口、阴道双重开口和双重肛门凹陷,肛门闭锁和直肠前庭瘘双侧。探查发现阑尾双重、结肠重复、子宫双重(双侧输卵管和卵巢继续存在)、直肠双重、肠旋转不良,盲肠位于腹部中央,肠系膜缺损,小肠通过该缺损疝入。肠道通过手术复位并修复了缺损。