Unveiling complexity: a case report on management of pyloric stricture in complex gastroschisis

Abstract Background Gastroschisis is a congenital defect of the abdominal wall with evisceration of bowels and stomach without a covering sac. Sutureless reduction of the abdominal contents can be done gradually using a silo. This condition may be associated with other gastrointestinal problems such as bowel atresia or stenosis, perforation, necrotizing enterocolitis, malrotation, or bowel dysmotility. Pyloric stricture post-sutureless silo reduction is a rare form of complex gastroschisis that has not been reported before in the literature. We discuss the diagnostic challenges and management of this rare case. Case presentation A premature female was born at 35 weeks, with a birth weight of 2.2 kg, and had gastroschisis. Evisceration of the stomach, small bowels, and large bowels can be seen via an abdominal wall defect. There was bowel matting at the jejunum and right colon, causing a narrowing effect. Small bowel contents were decompressed proximally into the stomach and aspirated via an orogastric tube. Abdominal contents were successfully reduced using a spring-loaded silo. The abdominal wall defect was covered with the umbilical stump and was allowed to heal spontaneously. Feeding was started after one month and increased to full enteral feedings. She developed recurrent episodes of vomiting and was treated for gastroesophageal reflux disease and bowel dysmotility. Despite optimal medical treatment, clinical observation showed a progressive nature of obstruction. Vomiting episodes became more frequent over time, and total tolerable feeds were progressively less in amount. An upper gastrointestinal contrast study showed holdup of contrast in the stomach with delayed emptying into the small bowel. Esophagogastroscopy confirmed a pinpoint opening at the pylorus. Laparotomy, excision of pyloric stricture, and gastroduodenostomy were done. The child recovered well after surgery and was discharged home. Conclusion Pyloric stricture is a rare sequel following sutureless silo reduction of gastroschisis. The pathophysiology behind this phenomenon remains unknown. Recurrent feeding intolerance in a patient with gastroschisis, not responding to medical treatment, warrants further investigations to rule out mechanical obstruction. Surgical resection and gastroduodenostomy are curative.

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Publication Details

Journal
Egyptian Pediatric Association Gazette
Published
2025-12-24
DOI
https://doi.org/10.1186/s43054-025-00492-2
Primary Topic
Congenital Anomalies and Fetal Surgery
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article
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article

Unveiling complexity: a case report on management of pyloric stricture in complex gastroschisis

Hooi Hooi Tan, Mohd Shahrulsalam Mohd Shah, Shung Ken Tan, Tammy Teoh Han Qi et al.
Egyptian Pediatric Association Gazette
Congenital Anomalies and Fetal Surgery
article

Unveiling complexity: a case report on management of pyloric stricture in complex gastroschisis

Hooi Hooi Tan, Mohd Shahrulsalam Mohd Shah, Shung Ken Tan, Tammy Teoh Han Qi, Mohan Arunasalam Nallusamy, Siti Nurr Syafeena Rais, Nurul Adzimah Kamaruddin
article en

Abstract

Abstract Background Gastroschisis is a congenital defect of the abdominal wall with evisceration of bowels and stomach without a covering sac. Sutureless reduction of the abdominal contents can be done gradually using a silo. This condition may be associated with other gastrointestinal problems such as bowel atresia or stenosis, perforation, necrotizing enterocolitis, malrotation, or bowel dysmotility. Pyloric stricture post-sutureless silo reduction is a rare form of complex gastroschisis that has not been reported before in the literature. We discuss the diagnostic challenges and management of this rare case. Case presentation A premature female was born at 35 weeks, with a birth weight of 2.2 kg, and had gastroschisis. Evisceration of the stomach, small bowels, and large bowels can be seen via an abdominal wall defect. There was bowel matting at the jejunum and right colon, causing a narrowing effect. Small bowel contents were decompressed proximally into the stomach and aspirated via an orogastric tube. Abdominal contents were successfully reduced using a spring-loaded silo. The abdominal wall defect was covered with the umbilical stump and was allowed to heal spontaneously. Feeding was started after one month and increased to full enteral feedings. She developed recurrent episodes of vomiting and was treated for gastroesophageal reflux disease and bowel dysmotility. Despite optimal medical treatment, clinical observation showed a progressive nature of obstruction. Vomiting episodes became more frequent over time, and total tolerable feeds were progressively less in amount. An upper gastrointestinal contrast study showed holdup of contrast in the stomach with delayed emptying into the small bowel. Esophagogastroscopy confirmed a pinpoint opening at the pylorus. Laparotomy, excision of pyloric stricture, and gastroduodenostomy were done. The child recovered well after surgery and was discharged home. Conclusion Pyloric stricture is a rare sequel following sutureless silo reduction of gastroschisis. The pathophysiology behind this phenomenon remains unknown. Recurrent feeding intolerance in a patient with gastroschisis, not responding to medical treatment, warrants further investigations to rule out mechanical obstruction. Surgical resection and gastroduodenostomy are curative.

Egyptian Pediatric Association GazetteVol. 73(1)
Universiti Sains Malaysia (MY), Hospital Pulau Pinang (MY), Hospital Universiti Sains Malaysia (MY), Hospital Seberang Jaya (MY), Institut Penyelidikan Veterinar (MY)
Openalex Percentile: Top 26%
Congenital Anomalies and Fetal Surgery
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