Title of article :
Gastric Perforation Associated with Congenital Diaphragmatic Hernia in a Neonate
Author/Authors :
Jiang, Yuan Children’s Hospital - School of Medicine - Zhejiang University - China , Sun, Bai-Ping Children’s Hospital - School of Medicine - Zhejiang University - China , Shi, Li-Ping Children’s Hospital - School of Medicine - Zhejiang University - China
Abstract :
and the amount of viscera herniated. Acute
gastrointestinal complications of neonatal CDH are
mainly caused by the incarceration of the stomach
and intestines[1], which are significantly reduced
by prenatal diagnosis and appropriate neonatal
treatment. Neonatal gastric perforation associated
with CDH is an unusual surgical emergency, the
symptoms of which may be quite nonspecific[1],
and the radiographic findings may show pleural
effusion and massive hydroperitoneum[2,3]. Rapid
diagnosis and appropriate treatment are essential.
We present a 4-day-old neonate with gastric
perforation and CDH, who was treated
successfully.
A 2.85 kg male infant was born at term by
Cesarean section. The US at 25 weeks was normal.
Milk feeding was accepted 2 hours after birth. He
presented with recurrent non-bilious vomiting
after meals during the first 3 days. Stools were
passed during this period. On day 4 of life he had
tachypnea and abdominal distension and greenish
vomiting and his condition deteriorated rapidly.
Then he was admitted to our hospital. On physical
examination there were marked abdominal
distension and decreased bowel sounds. The
auscultation revealed decreased air entry on the
lower left side of the chest. A nasogastric tube was
passed and it drained bilious aspirate. A supine
thoracoabdominal radiography showed an
opacified left lower lung field resembling pleural
effusion and the presence of gas in the left lower
chest with shifting of the mediastinum to the right
and a diffuse ground-glass opacity with paucity of
bowel gas (Fig. 1). An erect thoracoabdominal
radiography showed changes similar to the supine
radiography except for the presence of gas fluid
level in the left hemithorax (Fig. 1). Subsequent US
showed left hydrothorax and an abundant volume
of peritoneal fluid. Oral feeding stopped and he
was intubated soon after admission. Prompt
laparotomy was performed, which revealed the
posterolateral diaphragmatic hernia, with a hernia
orifice measuring 4×3 cm and consisting a large
part of the stomach. A perforation, 4 cm in
diameter, was located at the back wall of greater
curve of the stomach. An abundant amount of
yellow fluid was identified in the peritoneal cavity.
The defect of the diaphragm was closed primarily
and the perforation was repaired by two-layer
closure.
Keywords :
Gastric Perforation , Neonate , Congenital Diaphragmatic Hernia
Journal title :
Astroparticle Physics