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Pediatric Surgery
ABSITE Review
Tracheoesophageal Fistula
• RF: Premature/Low birth weight, Polyhydramnios
• 50% associated anomaly – GI, Cardiac, GU,
skeletal, CNS – (VACTERL)
TEF
• Most Common, Type C – 85%
• Dx – Inability to pass NGT/KUB/CXR
• Tx – R. Extrapleural thoracotomy at 4th intercostal
– TEF ligation/transection, restoration of esophageal continuity
– POD 5-7 esophagram, no leak begin oral feeds
• CX – GERD, leak, empyema, stricture, fistula
Malrotation
• Sx: Bilious emesis , <2yo
• Dx: upper GI-
– Birds beak 3rd part of duo, Ligament of Treitz is right of midline
• Tx – surgical emergency, resuscitate, immediate surgical
exploration
• Path: failure of CCW 270 rotation, Ladd’s bands
Malrotation
• Ladd’s Procedure
– Resuscitation
– Resect bands
– CCW rotation of
bowel
– Cecum in LLQ
– Duodenum in RUQ
– Appendectomy
Duodenal Atresia
• Sx – 24H old, Bilious
emesis, No abd distention
• 80% distal to ampulla
• RF polyhydramnios
• Associated anomalies
– 20% Trisomy 21
– Duodenal webs
Duodenal Atresia
• Dx – Double bubble
– NO distal air – if distal air
present concern for
midgut volvulus
• Tx – Duodeno-
duodenostomy
– Duodenal webs
Hirschsprung’s Disease
• Failure of neural crest cells
to migrate in caudal
direction–
– Absent ganglia in
myenteric/submucosal
plexus
• Sx – Failure to pass
meconium in first 24 hours;
distension, constipation,
emesis
• Dx – Barium enema; biopsy
confirm absence of
ganglion cells
Hirschsprung Disease
• Tx – Resect colon
proximal to where
ganglion cells appear
• Pull through procedure
(Soave, Duhamel)
• Hirschsprung colitis- abd
distension, foul smelling
diarrhea, sepsis
• Resuscitate, antibiotics, rectal
irrigation and washout
• Colectomy with temporary
colostomy
Necrotizing Enercolitis (NEC)
• Sx- bloody stools after
first feeding in
premature infant
• Dx- KUB
– pneumatosis, portal V
gas
• Tx – NPO, NGT, Abx,
serial Abd X-rays
NEC
• Indications for OR –
– Free air, peritonitis
– Abd wall
erythema/cellulitis
– Electrolytes
– Worsening distention
• Resect affected
intestine, end
ileostomy, mucous
fistula
• Reanastamose 4-6
weeks
Hypertrophic Pyloric Stenosis
• Thickening of pylorus,
Gastric outlet
obstruction
• Presents 3-6 weeks old
• Projectile, non bilious
emesis
• 4:1 M:F, palpate
“olive” in 50%
Hypertrophic Pyloric Stenosis
• Dx – U/S >4mm thick, >14mm long
• Tx
– Resuscitate first, correct lytes
• Hypochloremic, hypokalemic metabolic
alkalosis
– Pyloromyotomy (Fredet-Ramstedt)
Intussusception
• Invagination of intestines –lead points
– Lymphoid hyperplasia
– Meckel’s
– Lymphoma
• 3 months to 3 years old
• Sx- RUQ pain, Currant Jelly Stool, sausage mass
• Tx- reduce with air-contrast enema
• OR – Unsuccessful reduction, 3rd episode,
Peritonitis, free air
– Pressure to distal and squeeze out proximal.
Meckel Diverticulum
• MCC of GIB in children
(50% LGIB <2yo)
• Omphalomesenteric duct
remnant, true diverticula
• Ectopic gastric (60%),
pancreatic (5-10%)
mucosa
• Meckel scan – identifies
gastric mucosa
Meckel’s Diverticula
• Tx – Segmental resection if Sx present
• Rule of 2’s
– 2% pop
– 2% Sx
– 2:1 M:F
– 2Ft proximal to ileocecal valve
– 2yo or less at presentation
– 2 types presentation – bleeding/obstruction
– 2 tissue types
Biliary Atresia
• Neonatal jaundice at >2weeks
• Conjugated Hyperbilirubinemia
• Dx –
– US/ERCP- atretic biliary tree
– elevated LFTs
• Liver Bx – Duct proliferation,
cholestasis, inflammatory infiltrate
• Tx
– Extra-hepatic: Kasai procedure
(hepaticoporto-jejunostomy
– Intra-hepatic: liver transplant
Gastroschisis
• No peritoneal covering
• Thickened, edematous,
shortened intestine
(exposure to amniotic
fluid)
• Tx- Saline soaked gauze,
Resuscitate, antibiotics,
protect bowel
– Silastic silo
Omphalocele
• Midline defect, through umbilicus
• Peritoneal covering with umbilical
cord attached, normal appearing
intestine
• Common associated abnormalities
– Cardiac, Pericardial, sternal,
Diaphragmatic, MSK, GI, GU
• Beckwith-Wiedemann syndrome –
Omphalocele, Hyperinsulinemia,
macroglossia
• Pentology of Cantrell –
Omphalocele, Cardiac, Percardium,
Sternal, Diaphragmatic
Congenital Diaphragmatic Hernia
• Pulmonary hypertension
• Bochdalek – Posteriolateral
• Morgagni –
Anterior/retrosternal
• Eventration- failure to fuse
• NGT in chest
• Repair via abdominal
approach
Neuroblastoma
• Neural Crest tissue, Adrenal (50%),
N-myc oncogene
• <2yo, asymptomatic mass
• Raccoon eyes, calcifications on X-
ray
• Labs – Elevated catecholamines,
VMA, metanephrines
• Sx – Abd mass, flushing, HTN,
Diarrhea, raccoon eyes
• <1 – 70% survival, >1 35% survival
• Good prognosis - <10 N-myc, Low
mitosis, Normal LDH,
catecholamines
Wilms Tumor
• From Kidney, 3-4 yo
• 10% Bilateral
• WAGR – wilms, aniridia, GU, MR
• Beckwith-Wiedmann
• Replaced renal parenchyma, No X-ray
calcifications
• Tx
– Unilateral – nephrectomy, chemo
– Bilateral – neoadjuvant chemo, neprho-sparing
surgery
Pulmonary Sequestration
• Does NOT communicate with
tracheobronchial tree
• Aberrant blood supply
• MC at LLL
• Intralobar – Drains through pulm V, no other
anomalies, resect due to bleeding risk
• Extralobar – drains through systemic V,
Associated with other anomalies, Observe and
delay resection until 6-9mo
Congenital Lobar Overinflation
• Air trapping “emphysema” hyperexpansion of
involved portion
• LUL most common
• Commonly found incidentally in asymptomatic
patients
• May mimic signs of Tension PNX with
mediastinal shift on CXR – do NOT place chest
tube as can be lethal
Mediastinal masses
• T-Cell lymphoma
• Teratoma
• Tumor (neuroblastoma, Neurofibroma, germ
cell, Ganglioneuroma)
• Thymic mass
• Bronchogenic cyst
Kasai
• Resect fibrotic gallbladder/extrahepatic biliary tree
• RNY, Roux limb sutured to transected porta hepatis –
re-establish bile flow from minute bile ducts
• Transplant – Failed Kasai, decompensated liver disease,
late diagnosis
Hemangioma
• MC tumor of childhood and infancy
• Appears at birth and grows rapidly in first
12 months but then involutes
• TX:
– Most resolve by 5-6yo
– If uncontrolled growth, impairs function,
persists after 8yo, then
• Oral steroids
• Laser or Resection

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Pediatric surgery ABSITE

  • 2. Tracheoesophageal Fistula • RF: Premature/Low birth weight, Polyhydramnios • 50% associated anomaly – GI, Cardiac, GU, skeletal, CNS – (VACTERL)
  • 3. TEF • Most Common, Type C – 85% • Dx – Inability to pass NGT/KUB/CXR • Tx – R. Extrapleural thoracotomy at 4th intercostal – TEF ligation/transection, restoration of esophageal continuity – POD 5-7 esophagram, no leak begin oral feeds • CX – GERD, leak, empyema, stricture, fistula
  • 4.
  • 5. Malrotation • Sx: Bilious emesis , <2yo • Dx: upper GI- – Birds beak 3rd part of duo, Ligament of Treitz is right of midline • Tx – surgical emergency, resuscitate, immediate surgical exploration • Path: failure of CCW 270 rotation, Ladd’s bands
  • 6. Malrotation • Ladd’s Procedure – Resuscitation – Resect bands – CCW rotation of bowel – Cecum in LLQ – Duodenum in RUQ – Appendectomy
  • 7. Duodenal Atresia • Sx – 24H old, Bilious emesis, No abd distention • 80% distal to ampulla • RF polyhydramnios • Associated anomalies – 20% Trisomy 21 – Duodenal webs
  • 8. Duodenal Atresia • Dx – Double bubble – NO distal air – if distal air present concern for midgut volvulus • Tx – Duodeno- duodenostomy – Duodenal webs
  • 9. Hirschsprung’s Disease • Failure of neural crest cells to migrate in caudal direction– – Absent ganglia in myenteric/submucosal plexus • Sx – Failure to pass meconium in first 24 hours; distension, constipation, emesis • Dx – Barium enema; biopsy confirm absence of ganglion cells
  • 10. Hirschsprung Disease • Tx – Resect colon proximal to where ganglion cells appear • Pull through procedure (Soave, Duhamel) • Hirschsprung colitis- abd distension, foul smelling diarrhea, sepsis • Resuscitate, antibiotics, rectal irrigation and washout • Colectomy with temporary colostomy
  • 11. Necrotizing Enercolitis (NEC) • Sx- bloody stools after first feeding in premature infant • Dx- KUB – pneumatosis, portal V gas • Tx – NPO, NGT, Abx, serial Abd X-rays
  • 12. NEC • Indications for OR – – Free air, peritonitis – Abd wall erythema/cellulitis – Electrolytes – Worsening distention • Resect affected intestine, end ileostomy, mucous fistula • Reanastamose 4-6 weeks
  • 13. Hypertrophic Pyloric Stenosis • Thickening of pylorus, Gastric outlet obstruction • Presents 3-6 weeks old • Projectile, non bilious emesis • 4:1 M:F, palpate “olive” in 50%
  • 14. Hypertrophic Pyloric Stenosis • Dx – U/S >4mm thick, >14mm long • Tx – Resuscitate first, correct lytes • Hypochloremic, hypokalemic metabolic alkalosis – Pyloromyotomy (Fredet-Ramstedt)
  • 15. Intussusception • Invagination of intestines –lead points – Lymphoid hyperplasia – Meckel’s – Lymphoma • 3 months to 3 years old • Sx- RUQ pain, Currant Jelly Stool, sausage mass • Tx- reduce with air-contrast enema • OR – Unsuccessful reduction, 3rd episode, Peritonitis, free air – Pressure to distal and squeeze out proximal.
  • 16. Meckel Diverticulum • MCC of GIB in children (50% LGIB <2yo) • Omphalomesenteric duct remnant, true diverticula • Ectopic gastric (60%), pancreatic (5-10%) mucosa • Meckel scan – identifies gastric mucosa
  • 17. Meckel’s Diverticula • Tx – Segmental resection if Sx present • Rule of 2’s – 2% pop – 2% Sx – 2:1 M:F – 2Ft proximal to ileocecal valve – 2yo or less at presentation – 2 types presentation – bleeding/obstruction – 2 tissue types
  • 18. Biliary Atresia • Neonatal jaundice at >2weeks • Conjugated Hyperbilirubinemia • Dx – – US/ERCP- atretic biliary tree – elevated LFTs • Liver Bx – Duct proliferation, cholestasis, inflammatory infiltrate • Tx – Extra-hepatic: Kasai procedure (hepaticoporto-jejunostomy – Intra-hepatic: liver transplant
  • 19. Gastroschisis • No peritoneal covering • Thickened, edematous, shortened intestine (exposure to amniotic fluid) • Tx- Saline soaked gauze, Resuscitate, antibiotics, protect bowel – Silastic silo
  • 20. Omphalocele • Midline defect, through umbilicus • Peritoneal covering with umbilical cord attached, normal appearing intestine • Common associated abnormalities – Cardiac, Pericardial, sternal, Diaphragmatic, MSK, GI, GU • Beckwith-Wiedemann syndrome – Omphalocele, Hyperinsulinemia, macroglossia • Pentology of Cantrell – Omphalocele, Cardiac, Percardium, Sternal, Diaphragmatic
  • 21. Congenital Diaphragmatic Hernia • Pulmonary hypertension • Bochdalek – Posteriolateral • Morgagni – Anterior/retrosternal • Eventration- failure to fuse • NGT in chest • Repair via abdominal approach
  • 22. Neuroblastoma • Neural Crest tissue, Adrenal (50%), N-myc oncogene • <2yo, asymptomatic mass • Raccoon eyes, calcifications on X- ray • Labs – Elevated catecholamines, VMA, metanephrines • Sx – Abd mass, flushing, HTN, Diarrhea, raccoon eyes • <1 – 70% survival, >1 35% survival • Good prognosis - <10 N-myc, Low mitosis, Normal LDH, catecholamines
  • 23. Wilms Tumor • From Kidney, 3-4 yo • 10% Bilateral • WAGR – wilms, aniridia, GU, MR • Beckwith-Wiedmann • Replaced renal parenchyma, No X-ray calcifications • Tx – Unilateral – nephrectomy, chemo – Bilateral – neoadjuvant chemo, neprho-sparing surgery
  • 24.
  • 25.
  • 26. Pulmonary Sequestration • Does NOT communicate with tracheobronchial tree • Aberrant blood supply • MC at LLL • Intralobar – Drains through pulm V, no other anomalies, resect due to bleeding risk • Extralobar – drains through systemic V, Associated with other anomalies, Observe and delay resection until 6-9mo
  • 27. Congenital Lobar Overinflation • Air trapping “emphysema” hyperexpansion of involved portion • LUL most common • Commonly found incidentally in asymptomatic patients • May mimic signs of Tension PNX with mediastinal shift on CXR – do NOT place chest tube as can be lethal
  • 28. Mediastinal masses • T-Cell lymphoma • Teratoma • Tumor (neuroblastoma, Neurofibroma, germ cell, Ganglioneuroma) • Thymic mass • Bronchogenic cyst
  • 29. Kasai • Resect fibrotic gallbladder/extrahepatic biliary tree • RNY, Roux limb sutured to transected porta hepatis – re-establish bile flow from minute bile ducts • Transplant – Failed Kasai, decompensated liver disease, late diagnosis
  • 30. Hemangioma • MC tumor of childhood and infancy • Appears at birth and grows rapidly in first 12 months but then involutes • TX: – Most resolve by 5-6yo – If uncontrolled growth, impairs function, persists after 8yo, then • Oral steroids • Laser or Resection