S11: carcinomas & cysts Flashcards

1
Q

Describe the difference in location of a renal cell carcinoma vs transitional cell carcinoma

A

Renal cell carcinoma – presents in the parenchyma of the kidney
Transitional cell carcinoma – from calyx to the bladder

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2
Q

Describe the epidemiology of RCC

A

Arise from tubular epithelium
Rare in children, peak incidence in 60–70-year-olds, more common in males
Risk factors: dialysis, smoking & obesity

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3
Q

Describe the presentation of RCC

A

Hematuria or incidental finding
Nonspecific symptoms – fatigue, weight loss & fever
Often metastasise before local symptoms develop
If advanced:
1) Small number can secrete PTH-rP (present with hypercalcaemia)
2) Large varicocele may be present

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4
Q

List investigations for RCC

A

Radiology – ultrasound/CT scan
Endoscopy – flexible cystoscopy
Urine – cystology (looks for cancerous cells in urine, not common to do for RCC)

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5
Q

Describe the treatment for localised RCC

A

Surveillance
Increasingly small tumours removed with partial nephrectomy to preserve some renal function
Large tumours: radical nephrectomy with removal of adrenal gland, perinephric, upper ureter & para-aortic lymph nodes

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6
Q

Describe the treatment for metastatic RCC

A

Little effective treatment for metastatic disease

Palliative treatment – target angiogenesis (limit blood supply to growing tumour)

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7
Q

Describe the presentation of TCC

A

Hematuria
Incidental finding on imaging (USS or CT)
Weight loss, loss of appetite
Signs/symptoms of obstruction

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8
Q

Describe the causes, diagnosis & treatment of bladder TCC

A

Causes: analgesic misuse, exposure to aniline dyes (used in industrial manufacture) & smoking
More common in males
Can be diagnosed & treated by transurethral resection of bladder tumour (TURBT)

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9
Q

Describe diagnosis of bladder TCC

A

Investigation via cystoscopy and biopsy allows histological examination & staging
Diagnosis based on cytological examination of urine to check for the presence of malignant cells & cystoscopy of lower urinary tract

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10
Q

What are the differential diagnoses for TCC?

A
Bleeding from the prostate 
RCC
UTI
Nephritic conditions 
Polycystic kidney disease
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11
Q

Describe the treatment of bladder TCC

A

Low risk non-muscle invasive: treated with TURBT +/- intravesical chemotherapy to bladder
High risk non-muscle invasive: TURBT + intravesical chemotherapy, intravesical BCG treatment, cystectomy
Muscle invasive cancer – cystectomy + radiotherapy/palliative care

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12
Q

What is a cystectomy?

A

Complete removal of the bladder
Small part of the ileum (conduit) is used to act as an exit for the urine
Urine goes into stoma bag

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13
Q

Describe the presentation and treatment of TCC of upper urinary tract

A

Presentation: haematuria, obstruction occurs early because renal pelvis projects directly into the pelvicalyceal cavity
Treatment: nephron-ureterectomy (kidney, fat, ureter, cuff of bladder)

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14
Q

Describe carcinoma of the prostate

A

Risk factors: increased age, family history, ethnicity (black>white>Asian)
Lesions are most commonly found in the periphery compared with the more central location of BPH
Presentation: symptoms of UTI, prostatism or metastatic disease in the bone causing bone pain
In asymptomatic men, elevated PSA can be found which indicates carcinoma of prostate

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15
Q

What is prostate specific antigen?

A

Causes of a raised PSA – prostate cancer, infection, inflammation, large prostate & urinary retention
Having normal PSA does not mean you do not have prostate cancer and vice versa (normal PSA, but abnormal feeling prostate on DRE)

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16
Q

Describe the presentation of prostatic carcinoma

A
Urinary symptoms 
Bone pain 
Raised PSA, biopsy 
Opportunistic finding from DRE
Incidental finding at transurethral resection of prostate
17
Q

What staging and grading is used for prostatic carcinoma?

A

Grade – Gleason classification
-grade 1: well differentiated tumour composed of uniform tumour cells
-grade 5: anaplastic diffuse tumour with cells showing great variation in their structure & high mitotic rate
Stage – TNM system

18
Q

Describe the diagnosis of prostatic carcinoma

A

Digital rectal examination: hard & irregular prostate
Ultrasound: prostatic mass
Increased PSA level in blood (not definite)
Biopsy of prostate
Radiographs & bone scans – used to stage the tumour

19
Q

What can develop in advanced prostate cancer?

A

Can develop sclerotic bone regions

‘Hot spots’ on bone scan

20
Q

Describe the treatment for localised prostate cancer

A

Surgery, hormone therapy & radiotherapy
Treatment depends on the stage of the tumour
-T1/T2: radical surgical resection of prostate may be curative
Local radiotherapy can be used if patient unfit for surgery
Surveillance

21
Q

Describe the treatment for advanced prostate cancer

A

Hormonal manipulation is beneficial since testosterone promotes tumour growth
Surgical castration
Medical castration – LHRH agonists, GnRH agonists
Side effects of castration: hot flashes, impotence, increase in breast size, weight gain & mood changes
Palliative care

22
Q

What are differential diagnoses for prostate cancer?

A
BPH
Prostatitis 
Urethral stricture 
Multiple myeloma 
Any neurological condition
23
Q

Describe polycystic kidney disease

A

Autosomal dominant
Presentation: 30-40 (passed onto kids before they knew it) years of age with complications of hypertension, acute loin pain and/or haematuria or bilateral palpable kidneys
Cysts can develop anywhere in the kidney – compress the surrounding parenchyma & impair renal function

24
Q

Why is genetic screening not used for polycystic kidney disease?

A

Not a useful tool unless many family members with the disease are available for linkage
Young children – screen on annual basis for elevated BP/urine dipstick abnormalities
Late teens – ultrasound can be performed (absence of cysts at this stage would make the disease unlikely)
Repeated when they are > 30 years – no cysts this time then, APKD is virtually excluded

25
Q

Describe the macroscopic and microscopic appearance of the cysts

A

Macroscopically – kidneys are large with yellow fluid-filled cysts replacing the parenchyma
Haemorrhage into the cysts can occur
Microscopically – cysts are lined by cuboidal epithelium
USS/CT scan shows bilateral enlarged kidneys with multiple cysts

26
Q

Describe the complications & treatment of polycystic kidney disease

A

Morbidity & mortality are often the result of hypertension, eg. MI & cerebrovascular disease (Berry aneurysm in brain)
Condition also leads to progressive CKD
Treatment: control BP & dialysis and renal transplant needed if end-stage renal failure develops