Oncological Emergencies Flashcards

(34 cards)

1
Q

what is malignant cord compression?

A

radiological evidence of indentation of the thecal sac secondary to cancer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

which cancers are associated most bone mets leading to malignant cord compression?

A

lung
breast
kidney
prostate
thyroid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

where in the spine do majority of malignant cord compression occur?

A

60% thoracic
30% lumbar
10% cervical

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

clinical features of cord compression?

A
  • pain (severe, progressive)
  • weakness (typically symmetrical)
  • UMN lesions (increased tone, hyperreflexia, upgoing plantars)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

difference in features between cord compression and cauda equina?

A

cord compression: back pain, paralysis, hyperreflexia, +ve babinskis

cauda equina: back pain radiculopathy, reduced anal tone, saddle anaesthesia, paralysis hyporeflexia, hypotonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Ix to diagnose cord compression

A

MRI = gold standard

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Mx of cord compression?

A
  • analgesia
  • VTE prophylaxis
  • high dose dexamethasone
  • radiotherapy as adjuvant to surgery (or stand alone if unable to undergo surgery)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what is malignant hypercalcaemia?

A

serum calcium >2.6mmol/L, secondary to malignant process

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what are the most common malignancies associated with hyperparathyroidism?

A

breast cancer
multiple myelom a
lymphoma
lung cancer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what are the 3 main mechanisms that cause malignant hypercalcaemia?

A

osteolytic mets
PTH - related protein (PTHrP) secretion
increased 1,25-dihydroxyvitamin D production

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

clinical features of malignant hypercalcaemia?

A

‘stones, bones, thrones, abdo groans, psychiatric mones’

renal stones
bone pain
polyuria
abdo pain
psychiatric features

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Ix to diagnose malignant hypercalcaemia?

A
  • serum calcium level calcium level >2.6
  • identification of underlying cancer

(measure PTH as in malignant hypercalcaemia the PTH should be suppressed compared to primary hyperparathyroidism)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Mx of malignant hypercalcaemia?

A

IV rehydration, calcitonin and bisphosphonate therapy

admit to hosp if serum calcium >3mmol/L

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what is neutropenic sepsis ?

A

fever >38 degrees OR features of sepsis in a pt with pt w/ neutrophil count of <0.5

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

causes of neutropenia?

A

genetic: congenital neutropenia, chediak-higashi syndrome
acquired: malignancy, infections, drugs, autoimmune

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

clincial features of neutropenic sepsis?

A

signs of infection: (e.g. pneumonia or UTI)

  • temperature
  • acute confusion
  • tachypnoea
  • low BP
  • tachycardia
  • low urine output
17
Q

Ix to diagnose neutropenic sepsis?

A

Ix to identify source of infection + evidence of organ dysfunction and complications

  • bedside
  • bloods
  • cultures
  • imagine e.g. CXR, LP, ECHO
18
Q

Mx of neutropenic sepsis?

A

SEPSIS 6:
1. give 02
2. IV access, take bloods
3. give IV abx
4. give IV fluids
5. measure urine output
6. measure lactate

19
Q

what is malignant SVCO?

A

obstruction to the flow of blood through the superior vena cava secondary to cancer (from direct tumour growth or lymphadenopathy)

20
Q

most common cancers to cause SVCO?

A

lung carcinoma (70-80%)
non hodgkins lymphoma (10%)

less common:
- thymic
- breast
- mediastinal germ cell tumours

21
Q

clinical features of SVCO?

A

dyspnoea, facial swelling, head fullness, cough, dysphagia, worsening on bending forward, facial plethora, upper limb oedema , distended neck and chest well veins
+ve pembertons sign

22
Q

Ix to diagnose SVCO?

A

CXR - showing abnormality e.g. mediastinal widening or malignant pleural effusion

CT = diagnostic

then diagnose malignancy: tissue biopsy + staging CT

23
Q

Mx of SVCO?

A

conservative: elevation of head and neck, o2 titrated to sats

stenting, radiotherapy and chemo = main tx but dexamethasone can be to reduce swelling

24
Q

what is tumour lysis syndrome?

A

metabolic disturbances arising from breakdown of malignant cells following initiation of treatment for malignancy

25
what electrolyte abnormalities do you get in tumour lysis syndrome?
hyperkalaemia hyperphosphataemia hypocalcaemia hyperuricaemia
26
consequences of electrolyte disturbance in tumour lysis syndrome?
AKI, arrythmias, sudden death
27
what type of malignancy is tumour lysis syndrome common in?
haematological malignancy
28
what factors are associated with developing tumour lysis syndrome?
- high proliferation rate - chemosensitivity - large tumour burden - pre existing metabolic disturbances - renal impairment
29
clinical features of tumour lysis syndrome?
(tend to occur within first 72 hours following initiation of treatment) lethargy n+v diarrhoea anorexia muscle cramps syncope pruritus arthritis fluid overload heamaturia tetany + parasthesia bronchospasm (wheezing)
30
what Ix are done to diagnose tumour lysis syndrome?
renal function, electrolytes, serum urate +/- urine dip urine microscopy serum lactate lactate dehydrogenase ECG cardiac monitoring
31
what monitoring needs to be done if a pt is at high risk of tumour lysis syndrome
renal function, electrolytes and serum urate regularly
32
how is the diagnosis of tumour lysis syndrome made?
based on the cairo-bishop definition lab diagnosis: 2 or more needed - uric acid >476micromol/L - K+ > 6mmol/L - phosphate >1.45mmol/L - calcium <1.75mmol/L AND clin diagnosis: 1 or more needed - serum creatinine >1.5 upper limit normal - cardiac arrythmia / sudden death - seizure
33
what prophylaxis can be given to patient who are at high risk of developing tumour lysis syndrome?
oral or IV hydration allopurinol rasburicase
34
how is tumour lysis syndrome managed?
hyperphosphataemia -> hydration + diet restriction hyperkalaemia -> IV calcium gluconate, insulin/dextrose infusion and neb salbutamol hypocalcaemia -> dont treat unless symptomatic in which give IV replacement renal impairement -> fluids rehydration, adjustment of drug doses, possibly haemofiltration