rare!A baby boy in Quanzhou was just born, and he was found to be found to be the esophagus and anus.

Newborn baby

Can't defecate, can't swall

Accompanied by symptoms such as fever, pneumonia

The situation is urgent, life -threatening!

recently

At Quanzhou Maternal and Child Health Hospital · Children's Hospital

Pediatric surgeon is one

Congenital high anal atresia combined with neonatal lock in the esophagus

Do minimally invasive surgery

The baby recovered well and was discharged smoothly

If the baby can't get out, he will spit foam

The chief physician of the pediatric surgery said that the baby was born in July. When he was born, the doctor found that he did not form a normal anal. Moreover, after further inspection, his esophagus was also a "dead end". Food could not enter the stomach and could not feed.

"In this case, the baby will cause suffocation to death due to malnutrition, dehydration, or not swallowing due to feeding. Because there is no way to swallow, the child's salva will flood back to his mouth and vomit like a crab like a crab. White foam, so this baby is also called 'crab baby'. "

In urgent situation, the doctor decided to perform minimally invasive surgery for the child and open up his esophagus and anus.

Doctors use thoracoscopy for babies to perform a whole hemp pipe pipe fistula ligation+esophageal reconstruction+horizontal colon. According to Zi Yongjuan, because the baby was just born one day, his body was very small. His esophageal was slightly thicker than that of cotton swab sticks. The surgical vision and operational space were limited, and the operation was very difficult.

After teamwork, the surgery was successfully completed. After surgery, the doctor had standardized treatment such as preventing wound infections, hemostasis, and liquid replenishment. The baby recovered well and was discharged smoothly. Recently, when the baby went to the hospital for review, all indicators were normal.

Congenital anal and esophageal atresia endanger the lives of newborns

According to Zi Yongjuan, congenital anal atresia and congenital esophageal lock are severe developmental deformities and life -threatening.

Congenital anal atresia is also called anal and anal aids. The disease is a common congenital digestive deformity. If the baby does not defecate 24 hours after birth, anal rectal malformations should be considered and checked in time.

If it is not treated in time, children's feces cannot be discharged, and intestinal obstruction, intestinal necrosis and intestinal perforation will occur clinically. Congenital anal atresia can treat diseases, and most children can defecate and live normally after surgery.

Congenital esophageal atresia is a serious congenital esophageal malformations, often combined with esophageal tracheal fistula. After the newborn is born, frequently spit white foam, or when he feeds the water for the first time, start vomiting after swallowing. After eating milk, coughing and blue face, you must be vigilant. Essence

Source: Minnan.com

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