Bischoff Andrea, Calvo-Garcia Maria A, Baregamian Naira, Levitt Marc A, Lim Foong-Yen, Hall Jennifer, Peña Alberto
Colorectal Center for Children, Division of Pediatric Surgery, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, ML 2023, Cincinnati, OH 45229, USA.
Pediatr Surg Int. 2012 Aug;28(8):781-8. doi: 10.1007/s00383-012-3133-3.
With the advance of prenatal imaging, more often pediatric surgeons are called for prenatal counseling in suspected cases of cloaca or cloacal exstrophy. This presents new challenges for pediatric surgeons since no specific guidelines have been established so far. The purpose of this review is to analyze our experience in prenatally diagnosed cloaca or cloacal exstrophy and to provide some guidelines for prenatal counseling of these complex congenital anomalies.
A retrospective review of the medical charts of patients with prenatally diagnosed cloaca and cloacal exstrophy who received postnatal care in our institution between July 2005 and March 2012 was performed. Representative images of prenatal studies were selected from 13 cases to illustrate different scenarios and the recommendations given. In addition, a review of the literature was performed to support our advice to parents.
Eleven patients were female and two patients were male. The postnatal diagnoses were cloacal exstrophy (6), cloaca (5), posterior cloaca variant (1), and covered cloacal exstrophy (1). The selected abnormal prenatal imaging findings in these 13 patients included hydronephrosis (12), neural tube defect (8), omphalocele (7), lack of meconium at expected rectal location (7), vertebral anomaly (7), non-visualize bladder (5), distended bladder (5), hydrocolpos (4), dilated or echogenic bowel (3), umbilical cord cyst (3), separated pubic bones (2), and the "elephant trunk" sign (2). The prenatal diagnosis was correct in 10 cases, partially correct in two cases, and it was missed in one case. All parents received prenatal counseling depending on the specific diagnosis.
The continuous technologic innovations in prenatal imaging make it possible to prenatally diagnose more complex anomalies including cloaca and cloacal exstrophy with increased levels of confidence and enhance the benefit of prenatal counseling. Together, these allow the parents to be better prepared for the condition and the care team to provide the best possible initial management in order to improve the outcomes of these challenging patients.
随着产前影像学的发展,小儿外科医生越来越频繁地被要求对泄殖腔或泄殖腔外翻的疑似病例进行产前咨询。这给小儿外科医生带来了新的挑战,因为目前尚未制定具体的指导方针。本综述的目的是分析我们在产前诊断泄殖腔或泄殖腔外翻方面的经验,并为这些复杂先天性畸形的产前咨询提供一些指导方针。
对2005年7月至2012年3月期间在我院接受产后护理的产前诊断为泄殖腔和泄殖腔外翻的患者的病历进行回顾性研究。从13例病例中选取产前研究的代表性图像,以说明不同情况及给出的建议。此外,进行文献回顾以支持我们给家长的建议。
11例患者为女性,2例患者为男性。产后诊断为泄殖腔外翻(6例)、泄殖腔(5例)、后泄殖腔变异型(1例)和隐匿性泄殖腔外翻(1例)。这13例患者中所选的异常产前影像学表现包括肾积水(12例)、神经管缺陷(8例)、脐膨出(7例)、预期直肠位置无胎粪(7例)、脊柱异常(7例)、膀胱不可见(5例)、膀胱扩张(5例)、阴道积水(4例)、肠管扩张或回声增强(3例)、脐带囊肿(3例)、耻骨分离(2例)和“象鼻”征(2例)。产前诊断10例正确,2例部分正确,1例漏诊。所有家长均根据具体诊断接受了产前咨询。
产前影像学的持续技术创新使得在产前能够更有信心地诊断包括泄殖腔和泄殖腔外翻在内的更复杂畸形,并提高产前咨询的益处。这些共同使家长能够更好地为病情做好准备,护理团队能够提供最佳的初始管理,以改善这些具有挑战性患者的治疗效果。