Guidry Bradley, Prien Christopher, Glithero Kyle J, Model Lynn, Hechtman Daniel
Department of Surgery, Maimonides Medical Center, Brooklyn, NY, United States of America.
Department of Surgery, Maimonides Medical Center, Brooklyn, NY, United States of America.
Int J Surg Case Rep. 2024 Jul;120:109877. doi: 10.1016/j.ijscr.2024.109877. Epub 2024 Jun 6.
Spontaneous gastric perforation of the neonate is a rare phenomenon with a high risk of mortality. Despite an uncertain etiology, an association with prematurity and low-birth weight has been demonstrated. Prompt surgical repair and intensive care remain imperative to survival.
A premature, low-birth weight male was born at 32 weeks and admitted to the NICU for respiratory distress syndrome. Forty-eight hours after birth he developed abdominal distention and an abdominal radiograph demonstrated pneumoperitoneum. Antibiotics were initiated and he was taken for emergent operative exploration. A 3 cm longitudinal perforation was identified in the greater curvature of the stomach. A two-layered repair was performed and a protective Stamm gastrostomy created. On postoperative day 10, an upper gastrointestinal contrast study demonstrated no evidence of leakage. After sustained clinical improvement, the initiation of oral feeding, and continued weight gain, the neonate was successfully discharged home.
The etiology of spontaneous gastric perforation remains a debate with several proposed mechanisms. In most cases, the neonate will present with abdominal distention and emesis. Although presentation and evidence of pneumoperitoneum on abdominal radiograph are suspicious for this pathology, definitive diagnosis is confirmed during operative exploration. Dedicated intensive care and prompt surgical repair are paramount to survival. Despite decreasing mortality rates, premature and low-birth weight neonates continue to have the lowest rates of survival.
We present a rare case of a premature, low-birth weight neonate who developed spontaneous gastric perforation and was successfully rescued using a coordinated multidisciplinary approach enabling prompt diagnosis and surgical repair.
新生儿自发性胃穿孔是一种罕见现象,死亡率很高。尽管病因尚不明确,但已证实与早产和低体重有关。及时进行手术修复和重症监护对于生存至关重要。
一名早产、低体重男婴于32周出生,因呼吸窘迫综合征入住新生儿重症监护病房(NICU)。出生后48小时,他出现腹胀,腹部X线片显示有气腹。开始使用抗生素,并对他进行紧急手术探查。在胃大弯处发现一个3厘米的纵向穿孔。进行了两层修复,并做了一个保护性的 Stamm 胃造口术。术后第10天,上消化道造影检查未发现渗漏迹象。经过持续的临床改善、开始经口喂养以及体重持续增加后,该新生儿成功出院回家。
自发性胃穿孔的病因仍存在争议,有几种提出的机制。在大多数情况下,新生儿会出现腹胀和呕吐。虽然腹部X线片上出现气腹的表现和证据对此病变可疑,但在手术探查期间可确诊。专门的重症监护和及时的手术修复对生存至关重要。尽管死亡率在下降,但早产和低体重新生儿的生存率仍然最低。
我们报告了一例罕见的早产、低体重新生儿发生自发性胃穿孔的病例,通过多学科协作的方法实现了及时诊断和手术修复,成功挽救了该患儿。