Smith Caitlin A, Avansino Jeffrey R, Merguerian Paul, Lane Victoria, Levitt Marc
Department of General and Thoracic Surgery, Seattle Children's Hospital, University of Washington School of Medicine, Seattle, Washington, United States.
Department of Urology, Seattle Children's Hospital, University of Washington School of Medicine, Seattle, Washington, United States.
European J Pediatr Surg Rep. 2021 Jan;9(1):e41-e45. doi: 10.1055/s-0041-1728719. Epub 2021 May 18.
Cloacal exstrophy is a rare malformation that presents as a lower midline abdominal wall defect which affects the gastrointestinal and genitourinary systems. The components of cloacal exstrophy characteristically include omphalocele, exstrophy of perineal structures, and imperforate anus. Most of these patients also have renal anomalies such as pelvic kidney, fused kidneys, or solitary kidneys. This congenital condition can also be associated with spinal issues, such as spinal dysraphism. When combined with spinal defects, it is referred to as the omphalocele, exstrophy, imperforate anus, and spinal defects (OEIS) complex, and is one of the most challenging surgical conditions to manage. Here, we present a unique case of a low-birth-weight patient with OEIS and a liver containing giant omphalocele and the novel surgical technique used to manage her cloacal exstrophy whereby the cecal plate was not separated from the bladder halves, but rather left for an autoaugment, and the ileum was connected to the hindgut.
泄殖腔外翻是一种罕见的畸形,表现为下腹中线腹壁缺损,影响胃肠道和泌尿生殖系统。泄殖腔外翻的特征性组成部分包括脐膨出、会阴结构外翻和肛门闭锁。这些患者中的大多数还存在肾脏异常,如盆腔肾、融合肾或孤立肾。这种先天性疾病也可能与脊柱问题有关,如脊柱裂。当与脊柱缺陷合并时,称为脐膨出、外翻、肛门闭锁和脊柱缺陷(OEIS)综合征,是最难处理的外科疾病之一。在此,我们报告一例低体重患者患有OEIS综合征,肝脏伴有巨大脐膨出,以及用于处理其泄殖腔外翻的新颖手术技术,即盲肠板未与膀胱两半分离,而是留作自体扩大,回肠与后肠相连。