Congenital pyloric atresia – nine new cases: Single-center experience of the long-term follow-up and the lessons learnt over a decade

Retrospective analysis of nine congenital pyloric atresia cases over a decade reveals late presentation (median 7 months) with nonspecific symptoms like failure to thrive. Upper GI endoscopy proved valuable for diagnosis in late presenters, with 89% survival and frequent associated anomalies (67%). Feeding jejunostomy may benefit malnourished patients before definitive repair.