Surgery - pyloric stenosis, lymphadenopathy, head injury, solid tumours Flashcards

1
Q

What are the clinical features of pyloric stenosis. (including epidemiology)

A

Due to hypertrophy of pyloric muscle.
Boys:girls = 4:1
There may be family history

Projectile vomiting in first few weeks of life (2-7 weeks)
Hunger after vomiting - until there is dehydration
Weight loss if delayed
Vomiting can result in hypochloric metabolic alkalosis (with hyponatraemia and hypokalaemia)

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2
Q

How is pyloric stenosis diagnosed

A

Test feed (milk)

Gastric peristalsis may be seen as a wave moving from left to right.

Pyloric mass (feels like olive) usually palpable in RUQ

If doubt, US is helpful

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3
Q

How is pyloric stenosis managed?

A

Correct fluids and electrolytes (with 0.45% saline and 5% dextrose with Potassium supplement)

Once corrected, pyloromyotomy can be performed

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4
Q

What are the differentials of cervical lymphadenopathy in children?

A

Infectious: EBV, CMV
rubella

Aadenovirus, enterovirus (viral URTI)

Bacterial lymphadenitis - staph, strep,

TB
Kawasaki disease (unilateral >1.5 cm)

Toxoplasmosis

Granulomatous disease:
Sarcoidosis
Hyper IGM syndrome

Neoplastic disease:
Most common >6 years:
Non-Hodgkin lymphoma ()
Hodgkin’s lymphoma

Most common in <6 year olds:
Acute lymphoblastic leukaemia
Acute myeloid leukaemia

Rhabdomyosarcoma
Neuroblastoma
Also non-Hodgkins

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5
Q

What investigations are indicated in cervical lymphadenopathy?

A

FBC
ESR

Monospot for EBV, CMV, toxoplasmosis
TB skin test
Anti-HIV test

Hepatic and renal function + urinalysis (systemic disease)
Lactate dehydrogenase, uric acid, calcium, phosphate, Mg if malignancy suspected

Bone marrow
Liver biopsy
CT or US guided LN biopsy

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6
Q

What are the causes of suppurative lymphadenitis?

A

Can be a consequence of strep pharyngitis

Staphylococcus aureus
Strep pyogenes
Yersinia
Bartonella henselae
TB
Lymphogranuloma venerum
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7
Q

What is suppurative lymphadenitis?

A

Invasion of LN by neutrophils, resulting in rapid swelling, capsular distension, edema, and eventual tissue necrosis.

There may be erythema

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8
Q

Which investigations may be indicated in lymphadenitis > 2 weeks?

A
FBC/ESR
Blood culture/ film
Serology - EBV, CMV, (monospot) HIV, toxoplasmosis 
Tuberculin test
CXR
Excision biopsy
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9
Q

What are indications for admission and CT scan in a head injury? (need for spinal imaging?)

A
Loss of consciousness >5min
Abnormal drowsiness
3 or more episodes of vomiting
Clinical suspicion of NAI
Post-traumatic seizure without history of epilepsy
GCS <15 (<14 if <1 year old)

Signs of basilar skull fracture (CSF leak from nose/ears, panda eyes, blood behind tympanic membrane)

<1 year old and bruise/swelling >5cm on head

Dangerous mechanism of accident (eg. high-speed road traffic accident)

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10
Q

Outline the evaluation of a child with head injury?

A

Always admit for 4-6 hours to observe any change in behavior.

ABCDE

Neuro exam.
Inspect for signs of basilar skull fracture (raccoon eyes, CSF leak from ear/nose, blood behind tympanic membrane)

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11
Q

What secondary damage can be caused by head injuries? (may need to know)

A

Airway obstruction leading to hypoxia.
Hypo or hyperglycaemia.

Reduced cerebral perfusion due to raised ICP or hypotension from bleeding.

Haematoma: extradural, subdural, intracranian

Infection from open wound

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12
Q

What is Wilm’s tumour

A

From embryonal renal tissue.
Commonest renal tumour of childhood.
80% present < 5 year old.

Large abdominal mass.
Otherwise usually well, but can have pain. anorexia, haematuria, HTN

80% cured

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13
Q

What is a neuroblastoma

A

Arise from adrenal medulla and sympathetic NS.

Most common < 5 years old.

Spectrum from benign (ganglioneuroma) to malignant (neuroblastoma)

Abdominal mass or along sympathetic chain.
Metastatic disease - bone pain

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14
Q

What is a sacrococcygeal teratoma

A

In Fetus/Infant.
On coccyx.
Usually BENIGN.
Can grow quite large. This can lead to polyhydramnios.

Usually presents before 5 months. The later, the higher the chance of malignancy.

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