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Published on: August 23, 2022
A rare case of multiple duodenal perforations in early infancy
Kiminobu Sugito1, Takeshi Kusafuka, Mikiya Inoue
1Division of Pediatric Surgery, Department of Surgery, Nihon University School of Medicine, Tokyo, Japan.
Insights
This case study details a premature infant experiencing duodenal perforation, likely from an ulcer. Surgical intervention was successful, with the infant showing normal growth post-operation.
Area of Science:
- Neonatal surgery
- Pediatric gastroenterology
- Gastrointestinal pathology
Background:
- Duodenal perforation is a rare neonatal emergency.
- Premature infants, especially those with low birth weight and respiratory distress, are at increased risk.
- Suspected peptic ulcer disease is a potential cause.
Observation:
- A 26-week premature infant presented with abdominal distension 98 days after birth.
- Radiographs confirmed massive pneumoperitoneum, indicating a perforated viscus.
- Exploratory laparotomy revealed two duodenal perforations.
Findings:
- The infant underwent direct closure of the perforations and intra-abdominal drainage.
- Postoperative complications included central urorrhagia secondary to hematencephalon.
- The patient achieved normal growth without duodenal ulcer recurrence.
Implications:
- This case highlights the successful surgical management of duodenal perforation in a very premature infant.
- Early diagnosis and surgical intervention are critical for favorable outcomes.
- Further research into the etiology and prevention of neonatal duodenal ulcers is warranted.
Abstract:
Duodenal perforation in early infancy is an uncommon condition. We describe a case of duodenal perforation from suspected ulcer. A premature boy was born at the gestational age of 26 weeks with a birth weight of 764 g. The Apgar score at 1 min was 3 and at 5 min had decreased to 2. He was given intermittent mandatory ventilation for one month after the birth. Ninety-eight days after birth, the infant's abdomen became distended. A supine and cross-table lateral radiograph of the abdomen revealed massive pneumoperitoneum. An exploratory laparotomy was performed, which revealed two perforations in the anterior wall of the first portion of the duodenum. The operation procedure was direct closure and intra-abdominal drainage. On the postoperative first day, he had central urorrhagia from hematencephalon. The patient's growth after surgery has been normal, with no recurrence of duodenal ulcer.
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