Urology - Renal Tumours Flashcards
What is most common renal tumour?
- Renal cell carcinoma (80% of renal tumours) - arise from renal tubules)
- Malignant tumours can be 1ry or 2ry but secondary tumours are rare (anatomy - higher up than rest of urology system)
RCC: epidemiology
- 80-90% of renal tumours
- age: 55ya
- Sex: M>F = 2:1
RCC: risk factors
- obesity
- smoking
- then
- dialysis: 15% of pts develop RCC
- 4% heritable
RCC: pathology
- Adenocarcinomas from proximal renal tubular epithelium
- Subtypes: clear cell (70%), papillary (15%), chromophobe (5%) and collecting duct (1%)
RCC: Presentation
- 50% of pts are discovered as incidental finding - have USS/CT for unrelated reason
- Triad (rare): haematuria, loin pain and loin mass
- Systemic: anorexia, malaise, wt loss
- Clot retention
- Invasion of left renal vein: varicocele (1%)
- Cannonball mets: SOB
RCC: paraneoplastic features
- EPO: polycythaemia
- PTHrP: hypercalcaemia
- Renin: HTN
- ACTH: Cushing’s syndrome
- Amyloidosis
RCC: potential avenues of spread
- direct: renal vein (varicocele on LHS)
- lymph
- haematogenous: bone, liver and lung
Ix
- Blood: FBC (check polycythaemia), ESR, U+E, ALP, Ca
- Urine: dip and cytology
- DRE!!
- Imaging: CXR (cannonball mets), US (mass), IVU (filling defect), staging CT/MRI CAP
What is the name of staging system for RCC and outline the steps
- Robson staging
1. Confined to kidney
2. Involves perinephric fat but not Garota’s fascia
3. Spread into renal vein
4. Spread to adjacent/distant organs
RCC: Mx - medical and surgical
- *These cancers are very resistant to chemotherapy and radiotherapy - v rarely used
- Medical: reserved for pts with poor prognosis
- Surgical: radical nephrectomy or consider partial if pt only has 1 kidney, very poor kidney function or small tumour
TCC/Pelviureteric tumours: epidemiology and risk factors
- 2nd most common renal cancer
- Age: 50-80
- Risk factors: smoking, amine exposure (rubber industry), cyclophosphamide
TCC/Pelviureteric tumours: pathology
- same as TCC of bladder but account for less than 20% of renal tumours
- highly malignant
- location: bladder, ureter and pelvis
TCC/Pelviureteric tumours: presentation
- Painless haematuria
- frequency, urgency, dysuria
- urinary tract obstruction
TCC/Pelviureteric tumours: Ix
- Urine cytology
- same bloods as RCC
- CT/MRI (KUB or staging CAP)
- IVU: look for filling defect
TCC/Pelviureteric tumours: Mx
- Nephro-uretectomy
- need very regular follow up b/c 50% subsequently develop bladder tumours :(
Wilm’s tumour: what is it? When does it present? What mutations is it associated with?
- Aggressive childhood tumour of primitive renal tubules and mesenchymal cells
- May be associated with: Chr 11 mutation or WAGR syndrome
- commonest intra-abdo tumour in <10ya, if caught early survival is high but can be rapid/aggressive and metastasise to lungs (Rx is radical nephrectomy and stage-dependant post-op Chemo)
Wilm’s tumour: presentation
- 2-5ya
- 5-10% are bilateral
- Abdo mass/pain
- haematuria
- HTN
- Aggressive: mets to lungs?
Other neoplasms: benign
- Cysts are very common
- Renal papillary adenomas
- Oncocytoma: eosinophilic cells with numerous mitochondria
- Angiomyolipoma: seen in tuberous sclerosis
- *Bening tumours commonly require nephrectomy to exclude malignancy
Other neoplasms: malignant
-SCC associated with infected staghorn calculus