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Idiopathic non-hypertrophic pyloric stenosis in an infant successfully treated via endoscopic approach
Wikrom Karnsakul1, Mary L Cannon, Stacey Gillespie
1Wikrom Karnsakul, Division of Pediatric Gastroenterology and Nutrition, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United State.
Insights
Endoscopic pyloric balloon dilation offers a safe and effective treatment for infants with non-peptic, non-hypertrophic pyloric stenosis, improving gastrointestinal transit and symptom resolution.
Area of Science:
- Pediatric Gastroenterology
- Minimally Invasive Surgery
Background:
- Non-peptic, non-hypertrophic pyloric stenosis is a rare condition in infants.
- Endoscopic pyloric balloon dilation is established for gastric outlet obstruction in older patients.
Purpose of the Study:
- To evaluate the safety and efficacy of endoscopic pyloric balloon dilation in an infant with non-peptic, non-hypertrophic pyloric stenosis.
Main Methods:
- Diagnosis of partial gastric outlet obstruction (GOO) confirmed by upper gastrointestinal series (UGI).
- Exclusion of other causes via ultrasonography and CT scan.
- Step-wise endoscopic pyloric balloon dilation over three sessions with increasing balloon diameters.
Main Results:
- Successful treatment with normal gastrointestinal transit after the first dilation session.
- Patient tolerated solid food without symptoms post-procedure.
- Endoscope passage confirmed pyloric patency after the final dilation.
Conclusions:
- Endoscopic pyloric balloon dilation is a safe initial approach for infants with non-peptic, non-hypertrophic pyloric stenosis.
- This minimally invasive technique can be considered before surgical pyloroplasty.
Abstract:
Non-peptic, non-hypertrophic pyloric stenosis has rarely been reported in pediatric literature. Endoscopic pyloric balloon dilation has been shown to be a safe procedure in treating gastric outlet obstruction in older children and adults. Partial gastric outlet obstruction (GOO) was diagnosed in an infant by history and confirmed by an upper gastrointestinal series (UGI). Abdominal ultrasonography and computed tomography scan excluded idiopathic hypertrophic pyloric stenosis, abdominal tumors, gastrointestinal and hepato-biliary-pancreatic anomalies. Endoscopic findings showed a pinhole-sized pylorus and did not indicate peptic ulcer disease, Helicobacter pylori infection, antral web, or evidence of allergic and inflammatory bowel diseases. Three sessions of a step-wise endoscopic pyloric balloon dilation were conducted under general anesthesia and a fluoroscopy at two week intervals using catheter balloons (Boston Scientific Microvasive(®), MA, USA) of increasing diameters. Repeat UGI after the first session revealed normal gastrointestinal transit and no intestinal obstruction. The patient tolerated solid food without any gastrointestinal symptoms since the first session. The endoscope was able to be passed through the pylorus after the last session. Although the etiology of GOO in this infant is unclear (proposed mechanisms are herein discussed), endoscopic pyloric balloon dilation was a safe procedure for treating this young infant with non-peptic, non-hypertrophic pyloric stenosis and should be considered as an initial approach before pyloroplasty in such presentations.
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