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Renal Cancer
Dr.B.Balagobi
MBBS (Col)MD(Surgery) MRCS Ed FRCS Urology(Eng)
Consultant Urological Surgeon
Introduction
• 7th most common cancer in UK, 3% of all
cancers
• Rising due to increase in Imaging (incidentalomas)
– more SRM(Small renal mass)
• Deadly cancer
– Most lethal urological malignancy with >40% dying their
disease as opposed to ~20% with prostate/bladder
• More common in males (1.5x)
Risk factors
• Smoking
• HT
• Obesity
• Acquired Renal cysts/Dialysis
• Hereditary /Genetic
– Eg:Von Hippel-Lindau(VHL) syndrome
• young age,B/L RCC,multifocal RCC
Anatomy
Pathology
• Tumor arises from PCT cells(Cortex of the kidney)
• Macroscopic appearance
– Yellow in cross section
– Variegated appearance
• Haemorrhage,Necrosis
• Microscopy: clear cells-75%
– due to abundant glycogen in the cytoplasm)
Pathology:RCC
• Histological subtypes
– Clear cell (75%)
– Papillary Type I (5%)
– Papillary Type II (10 %)
– Chromophobe (5%)
– Collecting Duct Tumour
Clear cell Papillary Chromophobe
Pathology:Spread
• Local spread:
– Perinephric fat,Renal sinus
– Gerota’s fascia
– Grows into the renal vein,IVC,Even RA
– Obstruct the left testicular vein L/S varicocele
• Lymphatic
– Para aortic LN
• Blood
– Lungs, Brain, Bone, Liver
Tumour inside
Right atrium
TNM Staging
Contributors to Prognosis
• Pathologic stage(TNM)
• Histological subtype
– Clear cell>papillary>chromophobe
• Fuhrman Grade(1-4)
• Performance status of patient
• Tumour Necrosis
Pathology:Renal lesion
• Benign
– Cysts
• Bosniak cysts
• Congenital:PCKD
– Oncocytoma
– Angiomyolipoma(AML)
– Renal adenoma
• Malignant
– Primary
• Renal cell carcinoma(RCC)
• Renal pelvic tumour(TCC)
– Secondary
Clinical Features
• Over 50% detected incidentally with imaging for other reasons(US,CT)
• Classic triad (10%): indicates locally advanced disease
– Painless Haematuria (20%)
– Flank Pain (20%)
– Loin mass (10%)
• L/S Varicocele
• Metstatic symptoms:
– Bone pain, Adult onset headache/fit, Pleural effusion
• Paraneoplastic syndrome present in ~20%
– Hypercalcaemia(PTHrP)
– Hypertension(Renin)
– Polycythaemia(Erythropoitin)
– Staufer’s syndrome(Non metastatic liver dysfunction)
– PUO
– Anaemia,LOA,LOW
Investigations
• UFR
– microscopic haematuria
• Renal function(S.Cr),S.Ca,PT/INR,ALP(bone mets)
• Imaging
– USS/Abd
– Contrast CT/Abdomen,pelvis,chest
• Heterogenous and enhancing renal mass
– Bonescan,PET Scan(rarely)
CT
CT Scan:Bosniak Classification Renal Cysts
BOSNIAK DESCRIPTION % MALIGNANT
I Simple cyst 0%
II Thin septa/fine calcifications <5%
IIF >3cm/nodular ~5%
III Thick irreg wall/solid non-enhancing areas ~60%
IV Enhancing solid component ~100%
Bosnia
Renal cancer:Treatment
Depends on:
• Tumour factors
– TNM stage :Localized/Metastasis
– Tumour size
– Position of tumour
• Patient factors
– Performance status,Age
– Status of contralateral kidney
• Surgeon factors
– Availability of facility
– Surgeon experience
Management of Small Renal mass
• SRM = less than 4cm
– 20% benign
– Grows 3mm/yr,3% risk of mets
• Rx options
– Active surveillance Vs Watchful waiting
• Old age,cormorbidities
– Partial(Nephron sparin surgery=NSS)/Radical
Nephrectomy
– Ablation:Cryo therapy(cold)/Radio frequency
ablation(RFA)(Hot)
Cryo Vs RFA
Management of Renal cancer
• Larger tumours
– Partial nephrectomy(PN) if possible
• Absolute indications:
– Solitary functioning Kidney(SFK),B/L RCC,CKD
– Usually Radical Nephrectomy(RN)
• Surgery options
– Open surgery
– Laparoscopic Surgery
– Robotic surgery
Metastatic Renal cancer
• 1/3 of patients presents with mets.
• 1/3 of surgically treated patients develop mets.
• Rx Options
– Targeted Therapy
• Tyrosine kinase inhibitors-TKI(Sunitinib)
• Immunotherapy(checkpoint inhibitors Eg:Nivolumab)
– Cytoreductive Nephrectomy
– Embolization
• Primary tumour poor response to chemo or radio
therapy.

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Renal Cancer latest.pptx

  • 1. Renal Cancer Dr.B.Balagobi MBBS (Col)MD(Surgery) MRCS Ed FRCS Urology(Eng) Consultant Urological Surgeon
  • 2. Introduction • 7th most common cancer in UK, 3% of all cancers • Rising due to increase in Imaging (incidentalomas) – more SRM(Small renal mass) • Deadly cancer – Most lethal urological malignancy with >40% dying their disease as opposed to ~20% with prostate/bladder • More common in males (1.5x)
  • 3. Risk factors • Smoking • HT • Obesity • Acquired Renal cysts/Dialysis • Hereditary /Genetic – Eg:Von Hippel-Lindau(VHL) syndrome • young age,B/L RCC,multifocal RCC
  • 5.
  • 6. Pathology • Tumor arises from PCT cells(Cortex of the kidney) • Macroscopic appearance – Yellow in cross section – Variegated appearance • Haemorrhage,Necrosis • Microscopy: clear cells-75% – due to abundant glycogen in the cytoplasm)
  • 7. Pathology:RCC • Histological subtypes – Clear cell (75%) – Papillary Type I (5%) – Papillary Type II (10 %) – Chromophobe (5%) – Collecting Duct Tumour Clear cell Papillary Chromophobe
  • 8. Pathology:Spread • Local spread: – Perinephric fat,Renal sinus – Gerota’s fascia – Grows into the renal vein,IVC,Even RA – Obstruct the left testicular vein L/S varicocele • Lymphatic – Para aortic LN • Blood – Lungs, Brain, Bone, Liver
  • 10.
  • 11.
  • 13. Contributors to Prognosis • Pathologic stage(TNM) • Histological subtype – Clear cell>papillary>chromophobe • Fuhrman Grade(1-4) • Performance status of patient • Tumour Necrosis
  • 14. Pathology:Renal lesion • Benign – Cysts • Bosniak cysts • Congenital:PCKD – Oncocytoma – Angiomyolipoma(AML) – Renal adenoma • Malignant – Primary • Renal cell carcinoma(RCC) • Renal pelvic tumour(TCC) – Secondary
  • 15. Clinical Features • Over 50% detected incidentally with imaging for other reasons(US,CT) • Classic triad (10%): indicates locally advanced disease – Painless Haematuria (20%) – Flank Pain (20%) – Loin mass (10%) • L/S Varicocele • Metstatic symptoms: – Bone pain, Adult onset headache/fit, Pleural effusion • Paraneoplastic syndrome present in ~20% – Hypercalcaemia(PTHrP) – Hypertension(Renin) – Polycythaemia(Erythropoitin) – Staufer’s syndrome(Non metastatic liver dysfunction) – PUO – Anaemia,LOA,LOW
  • 16. Investigations • UFR – microscopic haematuria • Renal function(S.Cr),S.Ca,PT/INR,ALP(bone mets) • Imaging – USS/Abd – Contrast CT/Abdomen,pelvis,chest • Heterogenous and enhancing renal mass – Bonescan,PET Scan(rarely)
  • 17. CT
  • 18. CT Scan:Bosniak Classification Renal Cysts BOSNIAK DESCRIPTION % MALIGNANT I Simple cyst 0% II Thin septa/fine calcifications <5% IIF >3cm/nodular ~5% III Thick irreg wall/solid non-enhancing areas ~60% IV Enhancing solid component ~100%
  • 19.
  • 20.
  • 22. Renal cancer:Treatment Depends on: • Tumour factors – TNM stage :Localized/Metastasis – Tumour size – Position of tumour • Patient factors – Performance status,Age – Status of contralateral kidney • Surgeon factors – Availability of facility – Surgeon experience
  • 23. Management of Small Renal mass • SRM = less than 4cm – 20% benign – Grows 3mm/yr,3% risk of mets • Rx options – Active surveillance Vs Watchful waiting • Old age,cormorbidities – Partial(Nephron sparin surgery=NSS)/Radical Nephrectomy – Ablation:Cryo therapy(cold)/Radio frequency ablation(RFA)(Hot)
  • 25. Management of Renal cancer • Larger tumours – Partial nephrectomy(PN) if possible • Absolute indications: – Solitary functioning Kidney(SFK),B/L RCC,CKD – Usually Radical Nephrectomy(RN) • Surgery options – Open surgery – Laparoscopic Surgery – Robotic surgery
  • 26.
  • 27. Metastatic Renal cancer • 1/3 of patients presents with mets. • 1/3 of surgically treated patients develop mets. • Rx Options – Targeted Therapy • Tyrosine kinase inhibitors-TKI(Sunitinib) • Immunotherapy(checkpoint inhibitors Eg:Nivolumab) – Cytoreductive Nephrectomy – Embolization • Primary tumour poor response to chemo or radio therapy.