GU Tract Cancers Flashcards
Where do renal cell carcinomas arise from?
Proximal renal tubular epithelium
Epidemiological factors of renal cell carcinoma
90% of all renal cancers
Mean age 55
F:M = 2:1
15% of haemodialysis patients develop RCC
Features of renal cell carcinoma
50% found incidentally Haematuria Loin pain Abdominal mass Anorexia, malaise and weight loss PUO - often in isolation
What is a rare feature of renal cell carcinoma?
Invasion of left renal vein compresses the left testicular vein causing a varicocele
Spread of renal cell carcioma
Direct - renal vein
Via lymph
Or haemotogenous (bone, liver, lung)
% who have mets at presentation with renal cell carcinoma
25%
Findings in blood in RCC
Polycythaemia due to increased erythropoietin production
ALP - mets
HTN from increased renin production
Imaging in RCC
US
CT/MRI
CXR - “cannon ball” mets in lung from RCC
Treatment of RCC
Radical nephrectomy
RCC usually radiotherapy and chemotherapy resistant
Can do nephron sparing surgery if small T1 tumour
Treatment of unresectable or metastatic RCC
Some have good response to biological therapies - angiogenesis target agents
eg. Sunitinib, Bevacizumab, Sorafenib
1st line treatment for patients with multiple poor risk factors
Temsirolimus improves survival better than interferon (previous treatment)
What is Wilms tumour?
Nephroblastoma
Childhood tumour of primitive renal tubules and mesenchymal cells
Chief abdominal malignancy in childhood
Presents with abdominal pain and haematuria
Incidence of prostate cancer
Increases with age and 80% of men over 80 years
Associations of prostate cancer
Family history 2-3x increased risk
High testosterone
Spread of prostate cancer
Local - seminal vesicles, bladder, rectum
Lymph
Haematogenously - sclerotic bone lesions
Presentation of prostate cancer
Can be asymptomatic
Or nocturia, hesistancy, poor stream, terminal dribbling or obstruction
Weight loss and bone pain - suggests bony mets
DRE in prostate cancer
May show hard, irregular prostate