Cancers Flashcards

1
Q

Definition of visible and non-visible haematuria

A

Visible = macroscopic or gross haematuria. Visible in urine, colouring it red/pink/brown.

Non-visible = microscopic. Blood is present on dipstick and urinalysis only.

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2
Q

what you look for on a dipstick and significant findings

A

Blood

Nitrites = specific for UTI. shows bacteria activity (infection)

Leukocytes = sensitive for UTI. shows inflammation

Protein = protein:creat ratio, signif proteinuria needs referal to nephrology

pH = signif in stones

glucose = signif in new diabetes eg. fungal balanitis

bilirubin
ketones
specific gravity

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3
Q

risk factors for urological malignancy

A

Bladder TCC =
smoking, occupational aromatic amine exposure

Bladder SCC =
long term catheters, recurrent UTI, bladder stones
Schistosomiasis (in endemic areas)

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4
Q

Common benign causes of haematuria

A
Infection eg. UTI
Parasitic eg. schistosomiasis
Trauma or recent surgery
Renal calculi
Nephrological causes eg. IgA nephropathy
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5
Q

Common malignant causes of haematuria

A
Kidney tumours (RCC, TCC)
Ureter tumours (TCC)
Bladder tumours (TCC, SCC, adenocarcinoma)
Prostate tumours (Benign prostatic hyperplasia, adenocarcinoma)
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6
Q

How to take a history of haematuria

A

History = duration, where in stream, clots, associated symptoms (LUTS), past uro MHx, smoking, occupational exposure, foreign travel, recent trauma, anticoagulants?

Abdo, external genitalia, DRE exam

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7
Q

Pathophysiology of RCC

A

Adenocarcinoma tumour of the renal cortex.

Derived from the epithelium of prox. convoluted tubule.

Often appears in the upper pole of the kidney.

Can spread through direct invasion to perinephric tissues, adrenal gland, renal vein, inferior vena cava.

Can spread through lymphatic system to pre-aortic and hilar nodes.

Can spread by haematogenous spread to bones, liver, brain, lugns.

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8
Q

Risk factors and of RCC

A
SMOKING
Obesity
Genetic disorders 
(eg. von Hippel-Lindau disease)
Industrial exposure to carcinogens 
(eg. cadmium, lead, aromatic hydrocarbons)
Dialysis
Hypertension
Anatomical abnormalities
(polycystic kidneys, horseshoe kdineys)
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9
Q

define a Paraneoplastic syndrome and list common ones associated with RCC

A

Rare clinical disorders triggered by an altered immune system response to a neoplasm.

Triggered by ectopic secretions of hormones by RCC =
Stauffer’s syndrome, hypercalcaemia (PTH), hypertension (renin), polycythaemia (due to erythropoetin), pyrexia, etc

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10
Q

Treatment options for RCC

A

TNM staging for treatment

Localised =

  • partial nephrectomy if small
  • radical nephrectomy if large (removes kidney, perinephric fat, local lymph nodes en bloc)
  • Percutaneous radiofrequency ablation OR lap/percutaneous cryotherapy for those unsuitable for surgery.
  • Renal artery embolisation for haemorrhaging disease.
  • Surveillance

Metastatic

  • Nephrectomy + immunotherapy (IFN-a or IL-2) for those fit for surgery
  • Biological agents such as tyrosine kinase inhibitors (Sunitinib, Pazopanib)
  • Metastasectomy (resection of mets)

N1 = regional lymph nodes
- Open nephrectomy and lymph node dissection

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11
Q

Define an Upper Tract Transitional Cell Carcinoma and how it presents

A

Uncommon

Presents with visible haematuria

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12
Q

What investigations would you do for a RCC

A

Routine blood tests

Urinalysis for non-visible haematuria and urine sent to cytology.

USS

abdo-pelvis CT with IV contrast to confirm
(+ additional chest for staging)

Bosniak classification to stage:
1 = benign, simple
2 = benign, mildly complex
2F = likely benign but need to follow up
3 = 60% chance of cancer
4 = definite RCC
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13
Q

how is a Upper Tract -TCC commonly treated

A

CT urogram then ureteroscopy + biopsy to confirm.

Small low grade tumours can be treated with laser ablation

Non metastatic cases can be treated with nephro-ureterectomy (laparoscopic if possible)

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14
Q

What is a Transurethral Resection of Bladder Tumour (TURBT) and how the histology is used to divide tumours into Ta/T1 and T2+

A

It involves resection of bladder tissue by diathermy during rigid cystoscopy.

Allows assessment of histological type (TCC or SCC), Grade (1,2,3) and Stage (Tis, ta, T1 or T2+)

If tumour is superficial (Ta/T1) then a single dose of intravesical mitomycin is given.

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15
Q

treatment of Non-Muscle-Invasive Bladder Cancer

A

Discuss at specialist MDT.

Carcinoma in-situ or T1 tumours
= resect via TURBT

Treat higher risk with adjunct intravesical therapy = BCG regimen.

  • Live attenuated mycobacterium bovis is given IV and reduces progression
  • BCG side effects = dysuria, freq, urgency, UTI, haematuria

Radical Cystectomy also offered for high risk, if initial treatments have failed.

Regular surveillance via cytology and cystoscopy

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16
Q

treatment of muscle-invasive bladder TCC

A

Radical cystectomy (complete removal of bladder)

Neoadjuvant chemo (typically cisplatin combination regimen)

Following radical cystectomy will require urinary diversion.

Regular follow-up with CT imaging

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17
Q

basic principles of the procedure of a radical cystectomy

A

Male = cystoprostatectomy

  • removal of bladder and prostate
  • urethra can be removed enbloc if needed
  • pelvic lymph node dissection

Female = anterior exenteration

  • remove bladder, uterus, tubes, ovaries, anterior vaginal wall
  • pelvic lymph node dissection
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18
Q

How is prostate cancer usually diagnosed

A

Localised disease presents with LUTS, weak urinary stream, increased freq, urgency.

In advanced disease present with haematuria, dysuria, incontinence, haematospermia, suprapubic pain, loin pain, rectal tenesmus.

In metastatic disease, presents with bone pain and unexplained weight loss

Sometimes it is picked up incidentally when performing DRE.

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19
Q

common risk factors for prostate cancer

A

increases with age

Family history of prostate cancer

Genetics (HPC1 or BRCA1/2 so ask about females in the family with breast cancer etc)

Afro-caribbean or african-american

Obesity, DM, smoking

20
Q

Function of PSA

A

Prostate specific antigen is a seminal anticoagulant that can be elevated with prostate cancer.

(however can also be raised with BPH, recent DRE, retention, UTI, etc)

21
Q

What are the risks and benefits of PSA screening for prostate cancer

A

Benefits
- reduces mortality

Risks

  • overdiagnosis and overtreatment
  • side effects with treatment etc
22
Q

What are the risks and benefits of a transrectal ultrasound guided (TRUS) prostate biopsy

A

Risks

  • adverse events like sepsis
  • negative biopsy does not exclude cancer

Transperineal template biopsies are more accurate and there is no sepsis. However expensive

23
Q

What is Gleason scoring

A

Prostate cancers are graded based upon their histological appearance.

Gleason score is the sum of the most common growth pattern + the 2nd most common growth pattern seen.

Low = Gleason 3+3 = 6
Intermediate = Gleason 3 + 4 = 7
High = Gleason 4+3 =7, 8, 9, 10
24
Q

How does “active surveillance” and “watchful waiting” for prostate cancer differ

A

Active surveillance is used for low risk disease (Gleason 3+3 =6).
Monitor PSA every 3 months, DRE every 6-12 months, re-biopsy every 1-3 years. If the disease progresses then you can treat radically.
Avoids unnecessary treatment if there is no progression.

Watchful waiting is used for older patients or those with comorbidities.
Palliative treatment with hormones is used and monitoring if they develop mets or become symptomatic.

25
Q

What are the radical treatments for localised prostate cancer

A

Discuss at specialist prostate cancer MDT meeting.

Base treatment on PSA, Gleason and T staging (TNM)

Radical Prostatectomy (usually robotic but can be lap or open)
SE = erectile dysfunction, stress incontinence, bladder neck stenosis

External beam radiotherapy and Brachytherapy are alternatives used for localised cancer.

Chemo for metastatic (docetaxel or cabazitaxel used with prednisolone)

26
Q

What are some common side effects to the radical treatments for localised prostate cancer

A

Radical Prostatectomy has side effects of incontinence and impotence

27
Q

How is the hypothalamo-pituitary-gonadal axis of testosterone regulation targeted in hormone therapy for advanced prostate cancer?

A

This is Androgen deprivation therapy.

  • Bicalutamide (testosterone receptor antagonist) for 28 days
  • LHRH analogue is injected after 14 days and this is repeated every month
  • when the LHRH agonists are given, testosterone levels go up (flare) before going back down.
    This can be avoided by giving the anti-androgen Bicalutamide
  • LHRH analogue acts on anterior pituitary (releases FSH and LH)
28
Q

What are some other systemic therapies for advanced prostate cancer

A

Dexamethasone

Docetaxel chemotherapy

Abiraterone/ Enzalutamide
(lower levels of serum testosterone in mets cancer)

Palliative care

29
Q

Describe the clinical features of testis cancer

A

a lump. solid mass inseparable from testis on clinical exam

systemic symptoms if extensive mets

30
Q

What are some commonly used testicular tumour markers and their significance

A

Alpha-fetoprotein (AFP) is specific to Non-seminomatous germ cell tumours

Beta-HCG is raised in Non-seminomatous germ cell tumours and 10% of seminomas

LDH is a marker of tumour bulk

31
Q

What is the lymphatic drainage of the testis and how does this influence surgical treatment of testis cancer?

A

Testes drain into the paraaortic lymph nodes. Scrotum drains into the inguinal lymph nodes.

Surgical treatment is an inguinal orchidectomy unless there is lots of mets (then chemo first).
Offer sperm banking to those under 55.

Retroperitoneal lymph node dissection for NSGCT masses after chemo.

32
Q

What kind of cancer is testis cancer

A

Majority are germ cell tumours.

These germ cell tumours can be split into Non-seminomatous germ cell tumours and Seminomas

33
Q

What kind of cancer is penile cancer

A

Squamous cell carcinomas

34
Q

where does penile cancer typically metastasise to

A

Primarily lungs and liver.

35
Q

Treatment for penile cancer

A

Excision (circumcision, glansectomy, partial or total penectomy)

May need inguinal or pelvic node dissection

Dynamic sentinal node biopsy

36
Q

Investigations for haematuria?

A

Urinalysis
(nitrites and leukocytes indicate infection)

Baseline bloods (FBC, U&Es, clotting, PSA)

urinary protein levels in those with deranged renal function
(albumin:creatinine ratio or protein:creatinine ratio)

Flexible cystoscopy is gold standard for lower urinary tract

US KUB imaging (used in non-visible haematuria) and Ct Urogram (used in visible haematuria) used for upper urinary tract imaging

37
Q

3 types of urinary diversion that can be used in a radical cystectomy

A

Ileal conduit formation
(urine drains via a urostomy)

Neobladder
(ureters connected to new “bladder” made of small bowel, and connected to urethra)

Continuous Cutaneous Diversion (indianna pouch)

***Neobladder contraindicated if tumour extends to prostatic urethra.
Continent diversion contraindicated if renal/hepatic impairment or inadequate small bowel or cant catheterise.

38
Q

what type of cancer is prostate cancer?

A

Adenocarcinomas (95%)

39
Q

What further investigations other than a PSA are done to diagnose prostate cancer?

A

Transperineal Template biopsy
= low infection risk

Transrectal Ultrasound-guided (TRUS) biopsy
= there is a low risk of sepsis

multi-parametric magnet resonance imaging (mp-MRI)

abdo-pelvic CT to stage the prostate cancer

40
Q

common presentations of RCC

A

Haematuria (visible or non-visible)

flank pain

flank mass

Sometimes left sided masses can present with left varicocoele due to compression of left testicular vein.

Triad of loin pain, haematuria, palpable mass present in 15%

41
Q

What kinds of cancers are bladder cancers?

A

Transitional cell carcinomas (most common)
Squamous cell carcinomas
adenocarcinomas
sarcomas

42
Q

Risk factors for bladder cancer?

A

Smoking

Increasing age

exposure to aromatic hydrocarbons (eg. industrial dyes or rubbers)

Schistosomiasis infection (causes SCC)

Previous radiation to the pelvis

43
Q

How does bladder cancer present?

A

painless haematuria (visible or non-visible)

recurrent UTIs

LUTS (freq, urgency, feeling of incomplete voiding)

Locally advanced disease = pelvic pain

Metastatic disease = systemic eg. weight loss or lethargy

Usually unremarkable on clinical exam

44
Q

How is bladder cancer assessed for treatment and what investigations would you do?

A

TNM staging.

1) Urgent cystoscopy (via flexible cystoscopy under local anaesthetic)
2) Rigid cystoscopy under general anaesthetic for more definitive assessment if a suspicious lesion has been found previously.
3) biopsy tumour identified at rigid cystoscopy + potential resection via TURBT
4) CT staging before TURBT
5) Urine cytology (however poor sensitivity and specificity)

45
Q

How would you treat locally advanced or metastatic bladder cancer?

A

Chemotherapy
(cisplatin-based regimen or a caboplatin + gemcitabine-based regime)

Palliative options discussed when appropriate