MRCP revision battle 15.1: Renal cell carcinoma
MRCP revision battle 15.2: Von Hippel Lindau
MRCP revision battle 15.3: Neuralgic amyotrophy
MRCP revision battle 15.4: Porphyrias
MRCP revision battle 15.5: Kearns-Sayre
MRCP revision battle 15.6: Klinefelters
MRCP revision battle 15.7: Pellegra
MRCP revision battle 15.8: Neuroleptic malignant syndrome
MRCP revision battle 15.1: Renal cell carcinoma
Renal cell carcinoma, also known as hypernephroma or Gravitz Tumour, is a cancer arising in the proximal renal tubular epithelium.
It accounts for 85-90% of primary renal cancer.
The classic triad for renal cell carcinoma is:
- haematuria
- loin pain
- abdominal mass
Renal cell carcinoma may also be linked to pyrexias of unknown origin.
Another clinical sign to look out for is left variocele - caused by invasion of the left renal vein causing compression of the left testicular vein.
Factors associated with developing renal cell carcinoma include:
- smoking
- middle aged males (male:female 2:1)
- Von-Hippel Lindau syndrome (wait for the next battle if you don't know that that is)
- tuberous sclerosis
- acquired cystic kidney disease in renal failure
25% of patients with renal cell carcinoma have mets at presentation. The commonest mets are bone, liver and lung.
Endo effects associated with renal cell carcinoma include:
- erythropoietin --> polycythaemia
- PTH --> raised calcium
- renin --> raised BP
- ACTH
Treatment is surgery. If mets are present IL-2 or interferon alpha may also be considered.
There is a 45% 5 yr survival.
Now on to meet Von-Hippel-Lindau syndrome...