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Published on: November 30, 2010
Hypertrophic pyloric stenosis in an older child: a rare presentation with successful standard surgical management
Minu Bajpai1, Amit Singh, Shasanka Shekhar Panda
1Department of Pediatric Surgery, All India Institute of Medical Sciences (AIIMS), New Delhi, India.
Insights
Infantile hypertrophic pyloric stenosis typically affects newborns. This case highlights an unusual presentation in an 8-year-old child with persistent vomiting and poor weight gain.
Area of Science:
- Pediatric Gastroenterology
- Clinical Case Reports
Background:
- Infantile hypertrophic pyloric stenosis (IHPS) is a common neonatal surgical emergency.
- Typically presents within the first few months of life with non-bilious vomiting.
- Associated metabolic derangements like alkalosis and aciduria are well-documented.
Observation:
- An 8-year-old boy presented with a history of recurrent, long-standing non-bilious vomiting.
- The patient also exhibited poor weight gain.
- Notably, no significant metabolic abnormalities were detected during evaluation.
Findings:
- This case represents a rare, late-onset presentation of infantile hypertrophic pyloric stenosis.
- The absence of typical metabolic sequelae in this older child is unusual.
- Diagnostic challenges in atypical presentations of IHPS.
Implications:
- Suggests that IHPS may have atypical presentations beyond the neonatal period.
- Highlights the importance of considering IHPS in older children with unexplained vomiting and poor weight gain.
- Underscores the need for thorough diagnostic evaluation in suspected cases, even without classic symptoms.
Abstract:
Infantile hypertrophic pyloric stenosis is a disease of neonatal period usually manifest between the third and fourth weeks of life. Metabolic alkalosis and paradoxical aciduria are two common sequel of this entity. We report an unusual case of an 8-year-old boy who presented with recurrent, long-standing episodes of non-bilious vomiting and poor weight gain without any other metabolic derangement.
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