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Atresia pilórica aislada en un recién nacido varón: un informe de caso

Isam A A Taha¹, Mubarak H Ibrahim Hajalbashir¹, Fatima Eltahir¹

¹Department of Pediatric Surgery, Pediatric Surgery Center, National Ribat University Hospital, Khartoum, Sudan.

Journal of surgical case reports

|September 2, 2025

Resumen

La atresia pilórica (AP), un raro defecto congénito, requiere un diagnóstico y cirugía tempranos. Este informe detalla el manejo exitoso de la piloroplastia de un bebé sudanés con AP, que demuestra el procedimiento

Área de la Ciencia:

Cirugía pediátrica
Medicina neonatal
Desarrollo gastrointestinal

Sus antecedentes:

La atresia pilórica (AP) es una anomalía congénita rara que afecta a los recién nacidos, con una incidencia de aproximadamente 1 de cada 100.000 nacidos vivos.
La PA se presenta con tres tipos anatómicos principales: Tipo I (diafragmático), Tipo II (cordón fibroso) y Tipo III (separación completa).
El pronóstico está relacionado con la detección temprana, el tratamiento quirúrgico y la ausencia de anomalías asociadas.

Palabras clave:

Sudán informe de caso Anomalía congénita Obstrucción de la salida gástrica atresia pilórica aislada el recién nacido atresia pilórica Pyloroplasty (piloroplastia)

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