Paediatric Surgery Flashcards

1
Q

What are the Kocher criteria?

A
  1. Non weight bearing on affected side
  2. ESR > 40 mm/hr
  3. Fever
  4. WBC count of >12,000 mm3
    - when 4/4 criteria are met, there is a 99% chance that the child has septic arthritis
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2
Q

Commonest micro-organism for septic arthritis?

A

S.Aureus

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3
Q

Factors favouring septic arthritis diagnosis?

A

Factors favoring septic arthritis
WCC > 12
ESR >40
Inability to weight bear
Fever >38.5

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4
Q

Causes of absence of vas deferens?

A

Absence of the vas may be unilateral or bilateral
Cystic fibrosis CFTR gene mutations are the cause in 40% of cases
Some non CF cases are due to unilateral renal agenesis
Sperm harvesting may allow for assisted conception

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5
Q

Features of dermoid neck masses?

A

-Derived from pleuripotent stem cells and are located in the midline
-Most commonly in a suprahyoid location
-They have heterogeneous appearances on imaging and contain variable amounts of calcium and fat

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6
Q

Features of infantile haemangioma?

A

May present in either triangle of the neck
Grow rapidly initially and then will often spontaneously regress
Plain x-rays will show a mass lesion, usually containing calcified phleboliths
As involution occurs the fat content of the lesions increases

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7
Q

Features of pyloric stenosis?

A
  • M>F
  • 5-10% Family history in parents
  • Projectile non bile stained vomiting at 4-6 weeks of life
  • Diagnosis is made by test feed or USS
  • Treatment: Ramstedt pyloromyotomy (open or laparoscopic)
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8
Q

Features of oesophageal atresia?

A

Associated with tracheo-oesophageal fistula and polyhydramnios
May present with choking and cyanotic spells following aspiration
VACTERL associations

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9
Q

Features of Hirchsprung’s disease?

A

Absence of ganglion cells from myenteric and submucosal plexuses
Occurs in 1/5000 births
Full thickness rectal biopsy for diagnosis
Delayed passage of meconium and abdominal distension
Treatment is with rectal washouts initially, thereafter an anorectal pull through procedure

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10
Q

Features of biliary atresia?

A

Jaundice > 14 days
Increased conjugated bilirubin
Urgent Kasai procedure

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11
Q

Main risk factor for NEC?

A

Prematurity

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12
Q

Features of NEC?

A

-Early features include abdominal distension and passage of bloody stools
-X-Rays may show pneumatosis intestinalis and evidence of free air
-Increased risk when empirical antibiotics are given to infants beyond 5 days
-Treatment is with total gut rest and TPN, babies with perforations will require laparotomy

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13
Q

Sites of ectopic testes

A

base of penis, femoral triangle and perineum, superficial inguinal pouch

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14
Q

1st line treatment of CF meconium ileus?

A

enemas of either dilute gastrograffin or N-acetyl cysteine.

It’s important to ensure the child is adequately hydrated first. They are contra indicated if there is a suspected underlying perforation.

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15
Q

Process behind unilateral cleft lip?

A

a failure of nasolabial ring fusion

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16
Q

Features of hypospadias?

A

Absent frenular artery
Ventrally opened glans
Skin tethering to hypoplastic urethra
Splayed columns of spongiosum tissue distal to the meatus
Deficiency of the foreskin ventrally

17
Q

Management of hypospadias?

A

No routine cultural circumcisions
Urethroplasty
Penile reconstruction

18
Q

Most common location of urethral opening in hypospadias?

A

On the distal ventral surface of the penis

19
Q

what is bilious vomitinga sign of ?

A

intestinal malrotation

20
Q

What is intestinal malrotation volvulus treated with?

A

Ladd’s procedure

21
Q

what is a persistent vitello-intestinal duct?

A

persistent and ongoing discharge of small bowel content from the umbilicus

irritant to the surrounding skin

22
Q

Treatment of duodenal atresia?

A

Duodenoduodenostomy

23
Q

When should surgery for children with umbilical hernias occur?

A

Defer surgery until the child is 3 years or older.

24
Q

Features of congenital talipes equinovarus?

A

Equinus of the hindfoot
Adduction and varus of the midfoot
High arch

25
Q

Key anatomical deformities of talipes equinovarus?

A

Adducted and inverted calcaneus
Wedge shaped distal calcaneal articular surface
Severe Tibio-talar plantar flexion
Medial Talar neck inclination
Displacement of the navicular bone (medially)
Wedge shaped head of talus
Displacement of the cuboid (medially)

26
Q

Best conservative method for talipes?

A

ponseti method

27
Q

What is chonoanal atresia?

A

Congenital disorder with an incidence of 1 in 7000 births.
Posterior nasal airway occluded by soft tissue or bone.

cyanosis are usually worst during feeding. Improvement may be seen when the baby cries

28
Q

Subtype I osteogenesis imperfecta?

A

The collagen is normal quality but insufficient quantity.

29
Q

Subtype II osteogenesis imperfecta?

A

Poor collagen quantity and quality.

30
Q

Subtype III osteogenesis imperfecta?

A

Collagen poorly formed. Normal quantity.

31
Q

subtype IV osteogenesis imperfecta?

A

Sufficient collagen quantity but poor quality.

32
Q

Features of osteopetrosis?

A

Bones become harder and more dense.
Autosomal recessive condition.
It is commonest in young adults.
Radiology reveals a lack of differentiation between the cortex and the medulla described as marble bone.

33
Q

Features of nephroblastoma?

A

Nephroblastoma (Wilms tumours)
Usually present in first 4 years of life
May often present as a mass associated with haematuria (pyrexia may occur in 50%)
Often metastasise early (usually to lung)
Treated by nephrectomy
Younger children have better prognosis (<1 year of age =80% overall 5 year survival)

34
Q

Salter Harris Classification?

A

I ‘S’ = Slip (separated or straight across). Fracture of the cartilage of the physis (growth plate)
II ‘A’ = Above. The fracture lies above the physis, or Away from the joint.
III ‘L’ = Lower. The fracture is below the physis in the epiphysis.
IV ‘TE’ = Through Everything. The fracture is through the metaphysis, physis, and epiphysis.
V ‘R’ = Rammed (crushed). The physis has been crushed