Oncology Flashcards

1
Q

About how many new cases of childhood cancer are seen each year?

A

130

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2
Q

What are the most common children cancers?

A

Leukaemia - 33%
Brain tumours - 25%
Extracranial solid tumours - 40%

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3
Q

How is child cancer classified?

A

International classification of childhood cancer (ICCC)

Based un tumour morphology and primary site

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4
Q

What cancer does red light reflex detect?

A

Retinoblastoma

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5
Q

What is the most common age group to get cancer?

A

0-4

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6
Q

What are risk factors for childhood cancer?

A

Environment - radiation and infection ie EBV
Iatrogenic - chemotherapy and radiotherapy
Genes

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7
Q

What genetic conditions increase cancer risk?

A
Down's
Fanconi
Beckwith Weideman syndrome
Neurofibromatosis
Li-Fraumeni familial cancer syndrome
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8
Q

What is the typical presentation of child cancer?

A
Biological onset of disease
Symptom onset
Seek medical attention
Doctor recognises cancer as a possibility
Investigation - diagnosis - treatment
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9
Q

Who should be given immediate referral for cancer risk?

A

Patient with unexplained petechiae

Hepatosplenomegaly

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10
Q

Who should be given urgent referral for cancer risk?

A

Repeat attendance with the same problem with no clear diagnosis
New neuro symptoms, abdo mass

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11
Q

Who should be referred to hospital or for urgent investigation?

A

Pain on rest, back pain, waking with pain
Unexplained lump
Lymphadenopathy

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12
Q

What investigations are done for tumours?

A

Scans - MRI if possible
Biopsy/pathology
Tumour markers

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13
Q

How is cancer treated?

A
Multimodal therapy based on specific disease and extent
MDT approach
Chemotherapy
Surgery
Radiotherapy
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14
Q

What are acute risks of chemotherapy?

A
Hair loss
Nausea and vomiting
Mucositis
Diarrhoea/constipation
Bone marrow suppression - anaemia, bleeding, infection, thrombocytopenia
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15
Q

What are chronic risks of chemotherapy?

A

Organ impairment - kidneys, heart, nerves, ears
Reduced fertility
Second cancer

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16
Q

What are acute risks of radiotherapy?

A

Lethargy
Skin irritation
Swelling
Organ inflammation

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17
Q

What are chronic risks of radiotherapy?

A

Fibrosis/scarring
Second cancer
Reduced fertility

18
Q

What is the biggest cause of death in treatment?

19
Q

When is someone at risk of infection?

A

Neutrophils <0.5
Indwelling catheter
Mucosal inflammation
High dose chemo/stem cell transplant

20
Q

What are common infections on cancer treatment?

A
Pseudomonas aeruginosa
Enterobacteriaciae
Enterococci
Strep pneumoniae
Staph
Fungi
21
Q

How does sepsis/febrile neutropenia present?

A

Fever or low temp
Rigors
Drowsiness
Shock

22
Q

How is sepsis/febrile neutropenia managed?

A
IV access
Blood culture, FBC, U&amp;Es, LFTs, CRP
Lactate
CXR
ABC - oxygen, fluids
Broad spectrum antibiotics
If child very unwell - Intotropes and referral to PICU
23
Q

How does early raised ICP present?

A

Early morning headache/vomiting
Tense fontanelle - younger children
Increasing head circumference in young children

24
Q

How does late raised ICP present?

A
Constant headache
Papilloedema
Diplopia
Loss of upgaze
Neck stiffness
Status epilepticus
Reduced GCS
Cushings triad - low HR, high BP
25
How is raised ICP investigated?
Imaging mandatory - MRI best but CT is good for screening
26
How is raised ICP managed?
Dexamethasone if due to tumour - reduces oedema and increases CSF flow Neurosurgery - ventriculostomy
27
What pathological processes cause spinal cord impression?
Invasion from paravertebral disease Vertebral body compression CSF seeding Direct invasion
28
What cancer patients get spinal cord compression?
Ewing's sarcoma Medulloblastoma Neuroblastoma
29
How does spinal cord compression present?
Weakness Pain Sensory problems Sphincter disturbance
30
How is spinal cord compression managed?
Urgent MRI Start dexamethasone urgently to reduce peritumour oedema Definitive treatment with chemotherapy is appropriate when rapid response is expected Surgery
31
What is the main factor of outcome in spinal cord compression?
Severity of impairment
32
What is superior vena cava syndrome?
Tumour compresses SVC
33
What are common causes of SVC syndrome?
Lymphoma Neuroblastoma Germ cell tumour Thrombosis
34
How does SVC syndrome present?
``` Facial, neck, and upper thoracic plethora Oedema Cyanosis Distended veins Ill Anxious Reduced GCS ```
35
What are features of severe mediastinal compression?
``` Dyspnoea Tachypnoea Cough Wheeze Stridor Orthopnoea ```
36
What investigations are done for SVC/SMS?
CXR/CT chest | ECHO
37
How is SVC/SMS syndrome managed?
Keep upright and calm Urgent biopsy Look to obtain important diagnostic info without GA - FBC, pleural aspirate Definitive treatment is required urgently - chemotherapy/radiotherapy
38
What is tumuour lysis syndrome?
Tumour cells rapidly die and release intracellular contents leading to metabolic derangement
39
What are lab features of tumour lysis syndrome?
``` Raised potassium Raised urate Raised phosphate Decreased calcium Acute renal failure ```
40
How is tumour lysis syndrome treated?
ECG monitoring Hyperhydrate Diuresis Treat hyperkalaemia - NEVER GIVE POTASSIUM