Isolated pyloric atresia in a male neonate: a case report.

Pyloric atresia (PA) is an exceedingly rare congenital anomaly, affecting approximately one in 100 000 neonates. It is classified into three anatomical types: Type I (obliterating diaphragm), Type II (fibrous cord atresia), and Type III (complete separation between the stomach and duodenum). The prognosis depends on early diagnosis, appropriate surgical intervention, and the presence of associated anomalies.

Intrathoracic ectopic kidney with pulmonary sequestration: clinical and surgical insights: a case report.

Intrathoracic ectopic kidney is an extremely rare congenital defect that is frequently identified by accident because it is asymptomatic. Even more unusual is its link to pulmonary sequestration alone. This case report describes the clinical presentation of a 7-month-old child with a history of recurrent respiratory distress and chest infections since birth, who had shortness of breath, failure to thrive, and delayed developmental milestones.

Experience of the Sudanese doctors in surgery of conjoined twins.

Surgical separation of conjoined twins remains one of the most unique and rewarding experiences in the field of pediatric surgery, bearing in mind that this decision is their best chance of survival. These are the first reported cases of successfully separating omphalopagus conjoined twins by the liver in Sudan. After an emergency cesarean section, 62-day-old term-conjoined twins were referred to our pediatric surgery center.