Straňák Zbyněk, Pýcha Karel, Feyereislova Simona, Feyereisl Jaroslav, Rygl Michal
Third Faculty of Medicine, Charles University, Prague, Czech Republic.
Fetal Medicine Centre, Institute for the Care of Mother and Child, Prague, Czech Republic.
European J Pediatr Surg Rep. 2017 Jan;5(1):e51-e54. doi: 10.1055/s-0037-1606288. Epub 2017 Aug 31.
Delayed surgery after stabilization of infants with congenital diaphragmatic hernia (CDH) is an accepted strategy. However, the evidence favoring delayed versus immediate surgical repair is limited. We present an extremely rare case of a very low-birth-weight infant with prenatally diagnosed left-sided CDH and unexpected transmural bowel perforations developing within the postnatal stabilization period. A neonate born at 31st week of gestation with a birth weight of 1,470 g with antenatally diagnosed left-sided CDH presented with bowel dilation leading to transmural bowel perforations on the 2nd day of life. Meconium pleuroperitonitis resulted in severe systemic inflammatory response syndrome, pulmonary hypertension, multiple organ failure, and death. In neonates with CDH deteriorating under standard postnatal management, intestinal perforation, and early surgical intervention should be considered.
先天性膈疝(CDH)婴儿病情稳定后延迟手术是一种公认的策略。然而,支持延迟手术与立即手术修复的证据有限。我们报告了一例极为罕见的病例,一名极低出生体重儿,产前诊断为左侧CDH,在出生后病情稳定期间出现了意外的透壁性肠穿孔。
一名孕31周出生、出生体重1470克的新生儿,产前诊断为左侧CDH,出生第2天出现肠扩张并导致透壁性肠穿孔。胎粪性胸膜炎导致严重的全身炎症反应综合征、肺动脉高压、多器官功能衰竭及死亡。
对于在标准出生后管理下病情恶化的CDH新生儿,应考虑肠穿孔并尽早进行手术干预。