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surgical Flashcards

(49 cards)

1
Q

ddx neonatal bilious vomiting

A

Surgical

a. Malrotation with midgut volvulus
b. Intestinal atresia
c. Meconium ileus
d. Necrotising enterocolitis
e. Hirschsprung’s disease

Non-surgical

a. Sepsis
b. Meningitis
c. Omphalitis
d. Reflux

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2
Q

exomphalos vs gastroschisis

A

exomphalos:

  • herniation through defect at base of umbi
  • therefore protected by sac (membrane) continuous with umbi
  • poor outcome 10% survival
  • more associated with genetics - BW, T13, T18
  • if liver in sac, less likely aneuploidy risk

gastroschisis:
- herniation through abdo wall defect, usually to right of umbi
- no protective sac
- better outcome 90% survival
- AFP high
- cord paraumbi

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3
Q

consequences of CDH and long-term

A

pulmonary hypoplasia and pul HTN
malrotation
dextrocardia

long-term:
reflux, CLD, obstruction, recurrence of hernia

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4
Q

treatment of CDH

A

supportive: NGT
ventilate: HFOV vs CV, ECMO
treat pul HTN: NO, open PDA
surgical

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5
Q

what is diaphragmatic eventration

A

part of the diaphgram didnt muscularise good -> moves paradoxically
most is whatever, doesnt need repair

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6
Q

which TOF kind most common

A

type C = oesophageal atresia with distal TOF

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7
Q

types of TOF

A
A = atresia only
B = atresia + prox TOF
C = atresia + distal TOF
D = atresia + both TOF
E = h type = TOF no atresia
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8
Q

presence of air in stomach/bowel with a TOF must mean what type?

A

distal fistula present

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9
Q

how may TOFs present

A

US scan - polyhydramnios cant swallow fluid

birth - cant feed, vomiting/coughing, resp distress, infections, frothy mucous

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10
Q

which TOF type can present later?

A

H - no atresia, so stuff could go down to GI (or resp)

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11
Q

which type of TOF has worst prognosis?

A

A - pure atresia

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12
Q

pyloric stenosis

  • age
  • biochemical finding
A
  • 2-6 weeks

- hypokalaemic hypochloraemic met alkalosis (vomit up Cl and H2O, kidneys conserve Na/H2O and kick out H/K)

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13
Q

exam thoughts: pyloric atresia = what condition?

A

= EB

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14
Q

when does malrotation present?

A

most within first year

most in D1-D3 of life

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15
Q

most common type of intestinal atresia

A

duodenal

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16
Q

duodenal atresia radiological finding

A

double bubble

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17
Q

duodenal atresia - vomit colour and distension: comment

A

no distension

bilious if distal to ampulla - most common

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18
Q

exam thoughts: duodenal atresia = what syndrome

A

T21

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19
Q

duodenal atresia have to screen for what and why

A
a/w congenital abnormalities 
echo - CHD 
renal USS 
cxr - TOF
annular pnacreas
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20
Q

jejunoileal atresia - what kind of thing has gone wrong i.e. pathology

A

vascular shit

21
Q

non-operative Mx for mec ileus

A

NAC - water soluble enema

22
Q

NEC - clinical triad

A

bilious asps/vomiting
abdo distension
blood in stool

23
Q

pathogenesis of NEC

A

invasion of bad bacteria into wall
bad bacteria form gas + inflammation
ischaemic necrosis of wall

24
Q

risk factors for NEC

A

VLBW
aggressive enteral feeding
formula feeding
prolonged abx

25
NEC - some possible axr findings
i. Dilated loops of bowel consistent with ileus ii. Pneumatosis intestinalis (hallmark of NEC) = bubbles of gas in the small bowel wall iii. Pneumoperitoneum = occurs with perforation; gas outlining both sides of the bowel wall v. Portal venous gas
26
classic exam finding of intestinal perf
blue-black discolouration of abdominal wall
27
most common cause of neonatal obstruction
Hirschprung's
28
where in the colon is most Hirschprung disease
80% rectosigmoid
29
Hirschprung's - most common associated gene
RET protooncogene
30
Hirschprungs - how can they present
``` no mec in 48h bilious vomits abdo distension enterocolitis / obstruction / perf FTT constipation squirt sign ```
31
age of umbi hernia surgery vs inguinal
umbi: 2-3yo - 9/10 resolve spontaneously before then inguinal: 6:2 rule <6 weeks within 2 days, if <6 months within 2 weeks, if >6 months within 2 months
32
meckel's - rule of 2s
i. Most common in children under 2 ii. 2 times more common in males iii. Contains 2 types of tissue (pancreatic + gastric) iv. 2 inches long v. Found within 2 feet of the ileocaecal valve vi. Occurs in 2% of the population
33
age of intussusception
3mo-2yo
34
classic triad intussusception
abdo pain red currant jelly stool sausage shaped mass
35
examples of pathological lead points in intussusception
i. Meckel’s diverticulum ii. Polyps iii. Henoch-Schonlein purpura iv. Duplication cyst v. Other 1. Intestinal lymphoma (>6 months) 3. Adenovirus or rotavirus infection 4. Celiac disease 5. CF
36
US finding of intussusception
target sign
37
paraphimosis vs phimosis
phimosis cant retract - foreskin will balloon. physiological or there's been scarring e.g. circumcision, recurrent balanitis paraphimosis - can't put back a retracted foreskin
38
hypospadias - what
urethral meatus opens on underside of penis, and usually a/w chordee (bands pulling penis into curve) or hooded dorsal foreskin
39
exam thoughts - priapism = what disease
1/3 sickle cell develop priapism
40
when is foreskin fully retractable
3yo
41
inguinal hernia age
greatest in 1st year of life
42
when do most congenital UDT descend and why? so when do you need to refer for orchidopexy?
3mo - testosterone surge by 2mo so it wont descend after 4mo and need to refer orchidopexy by 6-12mo
43
male newborn with bilaterally UDT - exam thoughts - think of what??
is it even a boy tho? could be virilised female with CAH
44
whats the risks of a UDT
testicular cancer torsion infertility hernia - 90% have an associated patent tunica vaginalis
45
age groups of appendage torsion testicular torsion E-O hydrocele varicocele idiopathic scrotal oedema
appendage torsion - pre-pubertal testicular - neonatal and adolescents E-O - rare pre-puberty until has UTI with genitourinary issue!! usually adolescent with STI hydrocele - infants varicocele - peri-pubertal idiopathic scrotal oedema - 3-7yo
46
mumps orchitis occurs how long after parotitis
Mumps orchitis occurs 4-6days after parotitis**
47
main complications of varicocele
impaired fertility in 10-15%
48
pathophys of a non reactive hydrocoele | when to surgery and why
a. The patent processus vaginalis is narrow and enables peritoneal fluid, but not abdominal contents, into the cord structures b. Patent processus vaginalis often closes on its own, in the first 18 months of life surgery only if >2yo
49
exam thoughts: mec ileus = what?
90% = cystic fibrosis!!