Urology Flashcards

1
Q

how common is testicular cancer?

A
  • <1% call new cancer in UK are testicular cancer
  • incidence is highest in males aged 30-34
  • most common solid cancer in men aged 20-45, rare below 15 and above 60
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2
Q

what can be secreted by testicular cancers to pick it up on blood tests?

A
  • AFP - secreted by foetal yolk sac, liver and GI tract and appears in high levels in foetal blood
    • secreted in non-seminomatous germ cell tumours like embryonal, yolk and teratoma
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3
Q

how are testicular cancers classified?

A
  • germ cell: seminoma good prognosis, non-seminomatous which metastasises early
  • non germ cell: leading or Sertoli cell
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4
Q

what are some risk factors for testicular cancers?

A

history of cryptorchidism
Fix
racial origin - caucasian and Northern Europeans
maternal oestrogen
hx of sub fertility
contralateral cancer
HIV & seminoma

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5
Q

how does testicular cancer present?

A
  • most common - testicular lump
    • unilateral, painless
    • irregular, firm and fixed with no transillumination
  • evidence of metastasis - WL, back pain (retroperitoneal mets) and dypnoea
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6
Q

what are some differential diagnoses for a testicular lump?

A
  • tumours - seminoma or non-seminomatous germ cell tumours
  • epididymal cysts or spermatocele
  • trauma
  • haematoma
  • torsion
  • epididymitis
  • orchitis
  • strangulated hernia
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7
Q

how is a testicular lump investigated?

A

USS scrotum
CXR
bloods - FBC, U&E, LFT
tumour markers - AFP, LDH, bHCG
*urology MDT
trans-scrotal percutaneous biopsy
urgent radical inguinal orchidectomy +/- prosthesis
sperm banking - pre-orchidectomy and chemo
CT CAP - ideally 1/52 after orchidectomy

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8
Q

how is testicular cancer staged?

A

royal Marsden classification

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9
Q

how is testicular cancer treated?

A
  • MDT - surgery, radiotherapy, chemo
  • surgery - inguinal radical orchidectomy with fertility steps taken
  • NSGCT - orchidectomy, adjuvant chemo for vascular invasions, surveillance imaging and tumour markers
    • mets - chemo
  • seminomas - orchidectomy and surveillance monitoring, adjuvant chemo for high relapse risk
    • surveillance includes regular examinations, surveillance CT, tumour markers
    • mets - radiotherapy, chemo
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10
Q

what is the prognosis for testicular cancer?

A
  • 91% survive for 10+ years
  • depends on tumour type and stage
  • 5 year survival of patient with metastatic seminoma 88-95%
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11
Q

what is the pathophysiology of bladder cancer?

A
  • urothelial carci
    noma - AKA TCC *common
  • squamous cell - inner lining of bladder, can be caused by long term irritation or infection with schistosomiasis
  • adenocarcinoma - glandular cells in lining of bladder that make mucus
  • small cell - neuroendocrine cells
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12
Q

what are some classifications for bladder cancer?

A
  • non-muscle invasive - do not penetrate deeper layers of bladder wall
  • muscle invasive - penetrates into deep layers
  • metastatic - beyond bladder wall distally
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13
Q

what are some causes of haematuria?

A
  • kidney - tumour, trauma, stones, infection, nephropathy, PCKD
  • ureter - tumour, stone, stents, strictures
  • bladder - stones, cystitis, radiation cystitis, infection and trauma
  • prostate - tumour, prostatitis, BPH
  • urethra - stricture, foreign bodies
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14
Q

what are some risk factors of haematuria?

A
  • aromatic amine and dye use in occupation
  • smoking
  • infections - recurrent UTI, schistosomiasis and squamous cell carcinoma, untreated kidney stones
  • previous treatments - cyclophosphamide, radiotherapy to pelvis
  • industrial carcinogens used in industries like rubber, leather, hairdresser, textile, painting carcinogen exposure
    • up to 25y latency
  • FHx
  • diabetes - pioglitazone link
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15
Q

what would the presentation be like for bladder cancer?

A
  • 85% visible or non-visible haematuria
  • dysuria
  • frequency and urgency
  • poor flow
  • recurrent infections
  • lower back pain u/L
  • supra-pubic pain
  • constitutional sx - WL, loss of appetite, night sweats etc
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16
Q

how is bladder cancer staged and graded?

A

grading - 1 to 3 of well to poorly differentiated

staging - TNM

17
Q

what are the investigations carried out for bladder cancer?

A
  • Hx taking including occupation, DHx
  • urinalysis and cytology
  • FBC, U&E, PSA
  • DRE
  • USS KUB
  • flexible cystoscopy +/- biopsies
  • CT KUB or urogram (eGFR dependent)
  • CT chest, abdo, pelvis if muscle invasive
18
Q

what are the management options available for bladder cancers?

A

low risk - surveillance cystoscopies

intermediate - MMC or BCG
*MMC - anti-tumour abx
*BCG - attaches to urothelium leading to immune response

high risk - cystectomy
*TURBT

19
Q

how would you manage non-muscle invasive vs muscle invasive?

A

non - resection via TURBT as superficial

muscle invasive - radical cystectomy then radiotherapy

20
Q

how are those with bladder cancer followed up?

A
  • cystoscopy at 3 months and then 5 years followed up!
  • superficial have high rate of recurrence with 70% recurring within 3 years
    • more likely to be invasive
    • require routine follow-up with regular surveillance via cytology and cystoscopy
21
Q

what is the pathophysiology of renal cancers?

A

*RCC isadenocarcinoma of the renal cortex, arising predominantly from the proximal convoluted tubules, most often appearing in theupper pole of the kidney

85% renal tubular epithelial

22
Q

how do renal cancers spread?

A
  • direct extension to adrenals through renal capsule, renal vein, IVC, R atrium
  • lymphatic spread - hilar, para-aortic nodes
  • haematological spread - lung, bone, liver, brain
23
Q

what are the types of renal cancers?

A

clear cell renal cell carcinoma - 75%
papillary renal cell carcinoma
chromophobe renal cell carcinoma
collecting dust carcinoma.

24
Q

what is the most common presenting compliant of renal cancer?

A
  • 50% incidental
  • 50% haematuria
  • <10% classic traid - haematuria, pain and abdominal mass
  • PUO
25
Q

what are some risk factors of renal cancers?

A
  • Genetic
    • von-hippel-lindau (VHL) gene which is autosomal dominant
    • protein polybromo-1 (PRMR-1)
  • smoking
  • metabolic syndrome
  • chronic analgesic use
  • renal failure and dialysis
26
Q

what is the clinical presentation of renal cancers?

A

triad - haematuria, loin mass, loin pain
B sx
PUO
L varicocele
paraneoplastic syndromes

27
Q

why might renal cancers present with a left varicocele?

A

obstruction of L-testicular vein due to tumour in L. renal vein

28
Q

what paraneoplastic syndromes might you see in renal cancer?

A

anaemia - haematuria
polycythaemia - EPO
HTN
hypoglycaemia
cushings
hypercalcaemia
ectopic gonadotropins
stuffers syndrome

29
Q

how is renal cancer staged or graded?

A

grading - furham
staging - TNM

30
Q

how is a suspected renal cancer investigated?

A
  • FOC
  • urinalysis
  • USS
  • CT chest abdo pelvis
  • FBC, U&E, LFT
  • MRI - if features not clear on CT
  • biopsy - depending on size, MDT discussion, before partial nephrotectomy or cryotherapy
  • renogram - concern over function of contra-lateral kidney
  • bone scan if mets suspected
31
Q

how is renal cancers managed?

A

radical nephrectomy, or partial
surveillance
cryotherapy
nephro-ureterectomy
immunotherapy
chemotherapy
targeted therapy like MAB, TKI

palliative - radiotherapy, embolisation, conservative

32
Q

what is the prognosis of renal cancers?

A
  • 25% have mets at presentation
  • nephrectomy undergone survival 70% at 3 years and 60% 5 years
  • worse stage = poorer prognosis