一种治疗巨大脐膨出伴泄殖腔外翻的新手术方法。

Pub Date : 2021-01-01 Epub Date: 2021-05-18 DOI:10.1055/s-0041-1728719
Caitlin A Smith, Jeffrey R Avansino, Paul Merguerian, Victoria Lane, Marc Levitt
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引用次数: 0

摘要

摘要阴囊外翻是一种罕见的畸形,表现为腹壁下中线缺损,影响胃肠道和泌尿生殖系统。阴囊外翻的特征包括脐膨出、会阴结构外翻和肛门闭锁。这些患者大多伴有肾异常,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,如脊柱发育不良。当合并脊柱缺陷时,它被称为脐膨出、外翻、肛门闭锁和脊柱缺陷(OEIS)复合体,是最具挑战性的手术条件之一。在这里,我们提出了一个独特的病例,低出生体重的OEIS患者,肝脏含有巨大的脐膨出,并采用新颖的手术技术来治疗她的泄殖腔外翻,其中盲肠板没有与膀胱半部分分离,而是留给自己增加,回肠连接到后肠。
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A Novel Surgical Approach for the Management of Cloacal Exstrophy with a Giant Omphalocele.

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.

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