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Pediatric Surgery
LIMU
Acute pediatric conditions
Intussusption
Append
Congenital Posterolateral Diaphragmatic
Hernia (CDH)
One of most severe conditions of
neonate
Defect in diaphragm during early
fetal development
 left side most commonly affected
content of the hernia:
small bowel
colon
spleen
stomach
liver, kidney, tail of pancreatic
【Embryology】
week8~9 : division of coelomic cavity into the pleural
and peritoneal cavity by the diaphragm; a triangular area
in the posterolateral site was left open.
week10~12 :herniation occur through this opening into
the pleural cavity at the return of midgut
【pathophysiology】
1、Hypoplasia of the lung
Pulmonary weight (ipsilateral+contralateral)↓
Alveoli number↓
Hypertrophy of the media of pulmonary arteriole
Resistance of the vessels↑
2、Pulmonary hypertension
Abdominal viscera into the thoracic cavity → compression of the
lung, PaO2↓PaCO2↑→ acidosis, hypoxemia(PH<7.30)
→pulmonary vessels spasm →vessel resistance↑, right to left
shunting through patent ductus arteries and foramen
ovale↑→aggravate acidosis and hypoxemia in the body
circulation (fetal circulation syndrome)
diaphragmatic hernia
Clinical manifestations:
1,Severe respiratory distress,cyanosis, vomit
2,Breath sounds: diminished on the side of hernia
3,Heart sounds: deviated to the contralateral
chest
4,Scaphoid abdomen
【 diagnosis 】
Prenatal diagnosis
ultrasound: abdominal organ visible in the
fetal chest
diagnosis after birth
X-ray film:
•Typical air-filled stomach and bowels in the chest, which
continues into the abdominal cavity.
•Diaphram can not be seen at the affected side.
•Absence or scarcity of intestine in the abdominal cavity
Treatment
• Before delivery: cortisone could induce the
maturation of pulmonary tissue
• Preoperative preparation:
(1)mechanical ventilation with pure oxygen
(2)nasogastric tube to decompress
stomach and intestine
(3)semi-supine and inclined to
the ipsilateral side, keep warm
(4) i.v. fluid, correction of acidosis
(5)surgical repair without delay.
Esophageal Atresia
Tracheoesophageal Fistula
 Incidence: 1/3000
 associated anomalies common
VACTER VATER
【 clinical findings】
1、drooling saliva, unable to swallow
2、cough and chocking and may become cyanotic
after feeding
3、chemical and aspiration pneumonia
4、 recurrent bronchospasm in H type fistula.
【 diagnosis 】
1、prenatal diagnosis is suggested by
polyhydramnious.
2、nasogastric tube can not reach stomach.
3、 X-ray film show the coiling of the tube in
the upper mediastinum
Preoperative preparation
 supine and elevated to 30~40º
 Put catheter at the blind end of the
esophagus for continuous drainage
 oxygen inhalation, incubator
 i.v. fluid and broad-spectrum antibiotics
 surgical repair
 Prognosis: 98%~100% survival rate.
Hypertrophic Pyloric Stenosis
1、olive shaped mass:length 2~3.5cm,thickness
0.4~0.6cm,pale in color with consistency of
cartilage
2、Muscular hypertrophy of all the layers of the pylorus
causing the stenosis
First male in the family
Hypertrophic Pyloric Stenosis
【symptoms】
1、 projectile vomiting: onset:2-3 weeks after birth and
progressive with time; vomitus: non-bilious milk and milk
curds
2、 jaundice ????
3、 overall condition: dehydration, weight lose, hypo-
chloride metabolic alkalosis, oliguria
4、abdominal examination: distention of epigastrium,
visible gastric waves, presence of a palpable pyloric
tumor (unique physical sign) ?? After vomiting.
【Diagnosis】
1、typical vomiting and mass in the epigastrium
2、ultrsound: muscular thickness≥0.4cm,
SD=thickness×2/diameter≥50%
3、Radiological
1- distention of the stomach
2- elongated and narrow pyloric channel
3- delay in stomach emptying
Treatment】
Surgery ———— pyloromyotomy
Intestinal Atresia
and Stenosis
【 Diagnosis 】
1、prenatal ultrasound
2、Clinical findings:
bilious vomiting 24-48hrs after birth
3、X-ray:
duodenal atresia--Double bubble sign
jejunal atresia--triple bubble sign
low intestinal atresia--multiple air-fluid level
The only option is surgery
resection and anastomosis
Anatomy
1、distended segment: proxiaml colon enlarged
with muscular hypertrophy
2、stenosis segment:distal colon spasm
3、transitional segment:between distal and
proximal segments
Hirschsprung’s Disease
lack of ganglion cell in the neural plexus of the
affected segment of intestine
- spasm of affected segment with no normal
peristalsis
- internal sphincter spasm with no normal
defecation reflex
- Distension of proximal bowel with muscular
hypertrophy
【clinical findings】
Neonate:
1、emesis:bilious or feculent
2、abdominal distention
3、delayed passage of meconium
4、rectal examination:tightness of internal
sphincter,rectal emptiness,withdraw brings out meconium
and gas
Children and infant:
1、History of neonate constipation
2、Chronic abdominal distention
【Diagnosis】
Barium enema
- Demonstration of a spasmodic distal intestinal
segment with dilated proximal bowel
- Failure to evacuate barium from colon within 24hours
Anorectal Manometry
Rectal biopsy (Definitive diagnosis )
looking for the presence or absence of ganglion cells and
hypertrophied nerve trunks
【Complications】
Enterocolitis
Most frequently encountered and life-
threatening:
Clinical feature : diarrhea , sepsis
fever and abdominal distention
May Bowel necrosis and perforation
Treatment
Surgery .
Anorectal Malformations
(ARMs)
 One of the most frequently encountered
digestive tract abnormality
 Frequency is slightly higher in males
compared with females
 Associated anomaly: urogenital,another gastrointestinal
anomaly, cardiovascular, vertebra
ARM classification
Wingspread classification :
according to the relative position of rectal
end to the elevater ani:
high: above elevator ani
intermediate: within elevater ani
low: pass through elevater ani
ARM treatment
Aim:Rebuilt an anus with well functioning
anal sphincte
 High and intermediate imperforated anus
– colostomy at birth
– definitive surgery at 6-12months of age
 Low imperforated anus
– anoplasty after birth
Thank you!

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Ped. surgery.ppt

  • 3. Congenital Posterolateral Diaphragmatic Hernia (CDH) One of most severe conditions of neonate Defect in diaphragm during early fetal development  left side most commonly affected content of the hernia: small bowel colon spleen stomach liver, kidney, tail of pancreatic
  • 4. 【Embryology】 week8~9 : division of coelomic cavity into the pleural and peritoneal cavity by the diaphragm; a triangular area in the posterolateral site was left open. week10~12 :herniation occur through this opening into the pleural cavity at the return of midgut
  • 5. 【pathophysiology】 1、Hypoplasia of the lung Pulmonary weight (ipsilateral+contralateral)↓ Alveoli number↓ Hypertrophy of the media of pulmonary arteriole Resistance of the vessels↑ 2、Pulmonary hypertension Abdominal viscera into the thoracic cavity → compression of the lung, PaO2↓PaCO2↑→ acidosis, hypoxemia(PH<7.30) →pulmonary vessels spasm →vessel resistance↑, right to left shunting through patent ductus arteries and foramen ovale↑→aggravate acidosis and hypoxemia in the body circulation (fetal circulation syndrome)
  • 6. diaphragmatic hernia Clinical manifestations: 1,Severe respiratory distress,cyanosis, vomit 2,Breath sounds: diminished on the side of hernia 3,Heart sounds: deviated to the contralateral chest 4,Scaphoid abdomen
  • 7. 【 diagnosis 】 Prenatal diagnosis ultrasound: abdominal organ visible in the fetal chest
  • 8. diagnosis after birth X-ray film: •Typical air-filled stomach and bowels in the chest, which continues into the abdominal cavity. •Diaphram can not be seen at the affected side. •Absence or scarcity of intestine in the abdominal cavity
  • 9. Treatment • Before delivery: cortisone could induce the maturation of pulmonary tissue • Preoperative preparation: (1)mechanical ventilation with pure oxygen (2)nasogastric tube to decompress stomach and intestine (3)semi-supine and inclined to the ipsilateral side, keep warm (4) i.v. fluid, correction of acidosis (5)surgical repair without delay.
  • 10. Esophageal Atresia Tracheoesophageal Fistula  Incidence: 1/3000  associated anomalies common VACTER VATER
  • 11. 【 clinical findings】 1、drooling saliva, unable to swallow 2、cough and chocking and may become cyanotic after feeding 3、chemical and aspiration pneumonia 4、 recurrent bronchospasm in H type fistula.
  • 12. 【 diagnosis 】 1、prenatal diagnosis is suggested by polyhydramnious. 2、nasogastric tube can not reach stomach. 3、 X-ray film show the coiling of the tube in the upper mediastinum
  • 13. Preoperative preparation  supine and elevated to 30~40º  Put catheter at the blind end of the esophagus for continuous drainage  oxygen inhalation, incubator  i.v. fluid and broad-spectrum antibiotics  surgical repair  Prognosis: 98%~100% survival rate.
  • 14. Hypertrophic Pyloric Stenosis 1、olive shaped mass:length 2~3.5cm,thickness 0.4~0.6cm,pale in color with consistency of cartilage 2、Muscular hypertrophy of all the layers of the pylorus causing the stenosis First male in the family
  • 15. Hypertrophic Pyloric Stenosis 【symptoms】 1、 projectile vomiting: onset:2-3 weeks after birth and progressive with time; vomitus: non-bilious milk and milk curds 2、 jaundice ???? 3、 overall condition: dehydration, weight lose, hypo- chloride metabolic alkalosis, oliguria 4、abdominal examination: distention of epigastrium, visible gastric waves, presence of a palpable pyloric tumor (unique physical sign) ?? After vomiting.
  • 16. 【Diagnosis】 1、typical vomiting and mass in the epigastrium 2、ultrsound: muscular thickness≥0.4cm, SD=thickness×2/diameter≥50% 3、Radiological 1- distention of the stomach 2- elongated and narrow pyloric channel 3- delay in stomach emptying Treatment】 Surgery ———— pyloromyotomy
  • 18. 【 Diagnosis 】 1、prenatal ultrasound 2、Clinical findings: bilious vomiting 24-48hrs after birth 3、X-ray: duodenal atresia--Double bubble sign jejunal atresia--triple bubble sign low intestinal atresia--multiple air-fluid level The only option is surgery resection and anastomosis
  • 19. Anatomy 1、distended segment: proxiaml colon enlarged with muscular hypertrophy 2、stenosis segment:distal colon spasm 3、transitional segment:between distal and proximal segments
  • 20. Hirschsprung’s Disease lack of ganglion cell in the neural plexus of the affected segment of intestine - spasm of affected segment with no normal peristalsis - internal sphincter spasm with no normal defecation reflex - Distension of proximal bowel with muscular hypertrophy
  • 21. 【clinical findings】 Neonate: 1、emesis:bilious or feculent 2、abdominal distention 3、delayed passage of meconium 4、rectal examination:tightness of internal sphincter,rectal emptiness,withdraw brings out meconium and gas Children and infant: 1、History of neonate constipation 2、Chronic abdominal distention
  • 22. 【Diagnosis】 Barium enema - Demonstration of a spasmodic distal intestinal segment with dilated proximal bowel - Failure to evacuate barium from colon within 24hours Anorectal Manometry Rectal biopsy (Definitive diagnosis ) looking for the presence or absence of ganglion cells and hypertrophied nerve trunks
  • 23. 【Complications】 Enterocolitis Most frequently encountered and life- threatening: Clinical feature : diarrhea , sepsis fever and abdominal distention May Bowel necrosis and perforation Treatment Surgery .
  • 24. Anorectal Malformations (ARMs)  One of the most frequently encountered digestive tract abnormality  Frequency is slightly higher in males compared with females  Associated anomaly: urogenital,another gastrointestinal anomaly, cardiovascular, vertebra
  • 25. ARM classification Wingspread classification : according to the relative position of rectal end to the elevater ani: high: above elevator ani intermediate: within elevater ani low: pass through elevater ani
  • 26. ARM treatment Aim:Rebuilt an anus with well functioning anal sphincte  High and intermediate imperforated anus – colostomy at birth – definitive surgery at 6-12months of age  Low imperforated anus – anoplasty after birth