Surgical Paediatrics Flashcards

1
Q

What is this lesion?

A

Things to DDx:

  • congenital - feels part of scalp because its so hard and looks like a whole on XR. Periosteum holds it tight.
  • inflammatory
  • cancer

External angular dermoid cyst

  • Abnormality of embryogenesis
    • Abnormality of the fusion of the frontonasal + maxillary processes
  • During the fusion of these processes an epidermal cell get trapped in the fusion line
    • skin divides + peels in this cyst (cyst of peeling skin)
  • Often beneath the periosteum
  • takes 3-6 months to notice it.
  • treatment via simple excision, cut in the eyebrow.
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2
Q

Spot the Diagnosis?

A

Infantile capillary haemangioma (strawberry naevus)

  • regresses in 2nd year of life.
  • 1-2% of population
  • Common tumour of childhood (vascular malformation)
  • Only rx if:
  • in the visual plane (i.e. eyebrow), obstructs vision, 2o blindness
  • Other critical area (e.g. face)Lesions vulnerable to skin breakage → troublesome bleeding
    • Between toes
    • Around anus
  • Should be Ix to ensure Ø involving any deeper structures
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3
Q

What is this disease? Talk through examination findings?

A

Hydrocephalus

  • Large head
  • Setting sun eyes = rare pathognomonic sign of enlarged 4th ventricle
    • This child has a medulloblastoma
    • Obstructs outlet of 4th ventricle
    • Compresses oculomotor nucleus (controls eyelid) → retraction of upper lid
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4
Q

What is the diagnosis? talk through the origin?

A

Sacrococcygeal Teratoma

  • Teratoma arising from + attached to sacral tip / front of coccyx
  • Mixed solid + cystic areas arising from all embryological layers
  • Obvious at birth – can sometimes be larger than the baby
    • Excised within first week of life
    • Usually benign
    • Will quickly become malignant (5-15%)
  • IMMEDIATE referral
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5
Q

What is this condition? Talk through the classification

A

Cleft Palate - Pierre Robin Syndrome (mandible too small)

  • rare variant of cleft palate. not failure to join they can’t even get close because the tongue is in the way.
  • small lower jaw, receeding chin.

Description:

  • no hard palate
  • nasal septum visible (sphenoid)

Presentation:

  • nasal voice
  • normal swallowing just abnormal sucking so can still feed

Classification:

  • Primary cleft = lip + anterior hard palate
    • Failure of mesoderm to merge between frontonasal process + maxillary process of first brachial arch
    • 4-7/52 gestation
  • Secondary cleft = hard + soft palate behind incisive foramen
    • Failure of fusion of 2 hemispheric shelves
    • 7-10/52 gestation

Classification

  • Clefts of lip
  • Complete
  • Incomplete
  • Uni/bilateral
  • 2/3 will also have secondary palate
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6
Q

Spot the Diagnosis

A

Ambiguous genitalia

  • Phallus too large for clitoris, too small for penis
  • Proximal urethral opening, near labioscrotal (genital) folds
  • Genital folds remain unfused - gives appearance of labia / cleft scrotum
  • Testes are undescended / impalpable

May be an outward sign of life threatening internal disorder

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7
Q

Spot the Diagnosis?

A

Neck Lump - yet to be diagnoses.

  • inflammatory or hot its and infection. If not inflammed its cancer.
  • sentinel lymph nodes on the junction of the thoracic duct and the jugular system. Pus up thoracic duct is dead people.
  • Hodgkins and neuroblastoma in children.
  • in adults - sympathetic chain or lymphoma.
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8
Q

What is the problem shown in this picture?

A

Testicular Torsion

  • Unilateral pain in abdomen or testicle
    • Referred pain from scrotum.
  • get torsion of the:
    • epididymis
    • testis
    • hydatis of morgani
  • high riding testicle
  • +/- bellclapper deformity (congenital but happens after)
  • scrotal reddness = stops at the edge of the hemiscrotum
    • limited by the tunica vaginalis
    • if redness extends consider something else
    • blue appearance is because its ischaemic (haemorrhagic infarct)
  • PHx of resolving episodes of pain
  • two peaks in babies and >13. <11 in most common.
  • treat immediately - <6 hours to save it. and fix other testis so it cannot twist
  • torsion of the hydatid of morgnagni - can’t tell due to red skin and sore - common in onset of puberty as testerone at 10-11, armomatase as estrogen stimulates it.

DDx:

  • epididymitis - don’t do ultrasound, this is secondary to the ischaemic.
  • blue dot sign seen below there will be immediate system exploration of the appendix. Haemorrhage.
  • glands penis is generally the same size of the testis of a young boy.
  • torsion commonest at 13-15 - enlarged due to androgens in puberty.
    *
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9
Q

What is the problem shown in this picture?

A

Perinatal torsion - different from torsion in adolescent boy where testis is on longer mesentery

  • occurs in utero as testis are descending in tunica vaginalis
  • will be painless and hard at birth
  • baby is usually restless in womb that day - 35-36weeks. Gubernaculum eats its way through and starts making fibrous tissue and collagen to attach.
  • will involute over time

DDx:

  • teratoma can be form in the uterus.
  • US to make sure its not a tunour.
  • speramtic cord all twisted up.

‘vanishing testis’ - 6 months later the dead testis disapears. No one realises until afterwards.

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10
Q

Spot the Diagnosis

A

Idiopathic Scrotal Oedema

  • Cellulitis from perianal infection and sores on the bum.
  • Early childhood from a flea bite causing an allergic reaction
  • extends past the hemiscrotum
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11
Q

WHat is the diagnosis?

A

Varicocele

  • abnormal enlargement of the pampiniform venous plexus in the scrotum. Plexus of veins drains the testis.
  • common abnormality in adolescent boys (1 in 10). Anatomical variant.
  • asymmetric scrotum
  • ‘bag of worms’ will only be seen when vertical - will feel non-descript and squishy when horizontal
  • transillumination - 3rd world XR - easy way to see through the tissue.
  • sometimes painful due to too much blood, dragging feeling.
  • treated by tying of the veins and affects fertility by cooking the testis so sperm counts goes down.
  • indication for surgery - smaller testis will interfere with fertility, need an operation.
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12
Q

What is the diagnosis from this picture?

A

Nephrotic Syndrome

  • outside of the processus vaginalis (outside tunica vaginalis)
  • presents at 3am in the morning with:
    • generalised oedema - ‘can the child open their eyes?’
    • HTN
    • spherical scrotum (hydrocele with dumbbell shaped scrotum which is surgical)
    • may obliterate penis
    • looks transparent
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13
Q

What is the diagnosis from this picture?

A

Undescended Testis

  • 1 is normal sized (based on glans) and 1 is absent
  • the other will have compensatory hypertrophy
  • other testis is not palpable but left in the inguinal canal - under the fat, search for a moving target (in mesentery).
  • treatment is orchipexy at 6-12 months
  • can happen in cerebral palsy due to increased tone of cremaster muscle.
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14
Q

What is the diagnosis based on this history?

A
  • left hemiscrotum too big = hydrocele
  • on the other side:

Associated strangulated inguinal hernia:

  • undescended testis but encarcerated hernia
  • give pain relief and reduce it
  • fix undescended testis at the same time.
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15
Q

What is the Diagnosis? Explain the condition?

A

Branchial cleft defect - sinus or fistula

  • commonly 2nd cleft (connecting to tonsillar fossa) but sometimes 3rd (posterior o piriform fossa)
  • elective surgical excision to prevent recurrent salivary discharge.
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16
Q

What is the diagnosis?

A

Tongue Tied - ankylosglossia

  • abnormally short and thick frenulum
  • Complications:
    • cosmetic
    • function (speech and dental hygeine
    • interfere with breast feeding (controversy)
17
Q

What is the Diagnosis?

A

Meconium Ileus

  • sticky mucus blocks the ileum
  • occurs in Cystic Fibrosis
  • if distension from birth must have blocked above the ileocecal valve because otherwise the colon would resorb fluid in utero.
18
Q

What is the diagnosis?

A

Duodenal Atresia

  • wrinkly skin often on outside
  • congenital absence of complete closure of a portion of duodenum
  • see duoble bubble on USand AXR
  • 30% risk of Down’s syndrome
19
Q

What is the Diagnosis?

A

Malrotation Volvulus

  • commonly a few days after birth
  • S shape on contrast study (barium swallow)
  • offered LADDs procedure where untwisted and mesentery base is extended.
20
Q

What is the Diagnosis?

A

Gastroschisis

  • failure of full retraction of the umbilical hernia during development.
  • Genetically normal foetus
  • no membrane around the bowel like in omphalocele
  • inflammed appearance of the bowel
    • sterile urinary + fecal peritonitis from bowel + mesentery bathing in urine + meconium
  • wrap in glad wrap with thermal insulation
    • don’t twist bowel
    • dry gauze to stop it twisting
21
Q

Diagnosis?

A

Omphalocele (aka exomphalos)

  • failure of embryogenesis
  • failure of three layers to fully unite around the umbilicus during migration
    • very likely genetic abnormality
    • 50% other anomalities - often cardiac.
  • severe heat and water loss
  • wrap in glad wrap with insulation.
22
Q

What is the diagnosis based on the enema?

A

Hirschsprung’s disease

  • progressive distansion after birth
  • aganglionosis of the rectum which is in permanent spasm without neural control.
  • no submucosal plexus causing overgrowth of extrinsic nerves
  • treated with excision of the aganglionic distal gut
23
Q

What is the Diagnosis based on this picture?

A

Malrotation Volvulus

  • first few months of life.
  • S sign or corkscrew.
  • mesentery doesn’t appropriately migrate (two bases of attachment) are too close together.
  • Degree of twist is important
  • 720 causes arterial ischaemia
  • Requires surgery, Ladd’s procedure