Renal cell carcinoma Flashcards
What is renal cell carcinoma?
Malignancy arising from renal parenchyma/cortex (containing corpuscle, vasculature, PCT, DCT and cortical colleting ducts)
What is the aetiology of renal cell carcinoma? (x3)
- Mostly sporadic
- Von Hippel-Lindau syndrome (autosomal dominant condition)
- Succinate dehydrogenase related RCC (autosomal dominant condition)
- Birt-Hogg-Dube syndrome
What are the risk factors for renal cell carcinoma? (x3)
Smoking, obesity, hypertension
What are the main types of renal cell carcinoma? (x5)
- Clear cell RCC: gold-yellow solitary cortical lesions, and bilateral in von Hippel-Lindau. So-called because the cells have a clear cytoplasm
- Papillary RCC: originating from renal tubular cells
- Chromophobe tumours: characterised by not staining readily
- Multilocular cystic carcinoma: tumour contains multiple cysts
- Mucinous tubular and spindle cell carcinoma: composed of mucin, tumour cells forming tubules, and spindle cells
What is the epidemiology of renal cell carcinoma: Kidney cancers? Most common type? Gender? Age?
Accounts for 85% of kidney cancers. Clear cell RCC is the most common. More common in men. Increased incidence with age.
What are the signs and symptoms of renal cell carcinoma?
- Asymptomatic – most are incidental findings
- Triad of haematuria, flank pain, palpable abdominal mass
- May have systemic symptoms or hepatic impairment in paraneoplastic presentations
What is paraneoplastic syndrome? Types? (x4)
Consequence of cancer producing hormones or cytokines, or an immune response against the tumour. There are four types: endocrine dysfunction (tumour produces hormones), neurological dysfunction (usually from immune response to tumour cell antigen with concurrent auto-immune response to neurones containing similar-looking antigen), mucocutaneous dysfunction, and haematological (the latter two have same mechanism as neurological).
What are the investigations for renal cell carcinoma? (x4)
- BLOODS: U&Es show elevated creatinine from chronic renal insufficiency, high calcium is a marker of advanced disease, and FBC, LFTs, coagulation profiles can also be measured to assess for paraneoplastic syndrome
- URINALYSIS: haematuria and/or proteinuria
- ABDOMINAL USS: test for masses and lymphadenopathy
- CT/MRI: definitive test for diagnosis and staging. MRI indicated in patients where contrast dye is contraindicated e.g., renal insufficiency