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RENAL CELL CARCINOMA
PRAHLAD
VISHNU
SHRAWAN
MODERATOR-DR GURUPRASAD RAI
NAME- Mr X
AGE- 55 YEARS
SEX- MALE
ADDRESS- MANGALORE
OCCUPATION- FACTORY WORKER
PRESENTING COMPLAINTS
 HEMATURIA
 LOIN PAIN
 MASS IN LOIN
INSPECTION LOIN MASS
PALPATION MOBILE,NODULAR,
HARD,MOVES WITH
RESPIRATION
PERCUSSION DULL RENAL ANGLE
PATHOLOGY
GROSS– UNILATERAL, UPPER POLE,
LARGE ,GOLDEN YELLOW ,CIRCUMSCRIBED
CUT SECTION - AREA OF NECROSIS,CYSTIC CHANGE,
FOCI OF HAEMORRHAGE,THROMBUS
CLEAR CELL TYPE
INCIDENCE – 70%
GENETICS – SPORADICS & FAMILIAL
HISTOLOGY – CLEAR CYTOPLASM
WELL DIFFERENTIATED
INCIDENCE – 15%
GENETICS -SPORADICS & FAMILIAL
HISTOLOGY – PAPILLARY PATTERN
PSAMMOMA BODIES
PAPILLARY TYPE
TYPE INCIDENCE GENETICS HISTOLOGY
GRANULAR CELL
TYPE
8% SPORADIC
&
FAMILIAL
ABUNDANT
ACIDOPHILIC
CYTOPLASM
MARKED ATYPIA
CROMOPHOBE TYPE 5% MULTIPLE
CROMOSOMES
LOSS,
HYPODIPLOIDY
•MIXTURE PALE
CLEAR CELL WITH
PERINUCLEAR HALO
•GRANULAR CELL
SARCOMATOID TYPE 1.5%
-------
WHORLS OF
ATYPICAL
ANAPLASTIC
SPINDLE CELLS
COLLECTING DUCT
TYPE
0.5 TUBULAR &
PAPILLARY PATTERN
LYMPHATIC
SPREAD
PROLIFERATIVE TROMBUS
EXTENDS INTO IVC
CANNON BALL SECONDARIES
IN LUNG
VARICOCELE DUE TO
BLOCKED LEFT RENAL VEIN
BRAIN,BONE
HILAR & PARA AORTIC
LYMPHNODE
PERINEPHRIC PAD OF FAT,CALYCES
RENAL PELVIS
CLINICAL FEATURES
Renal cell carcinoma
(investigations, staging, treatment
and prognosis).
Investigations
1. Urine :- RBCs
2. IVU:- Shows mass lesion and irregular filling defect
3. U/S abdomen:- size, extension, lymph node, status of renal vein, spread to liver.
4. Ct scan:- Confirmatory
status of renal vein and ivc
lymph node status and tumour extension
5. CECT: Early lesions, function, spread and venous status.
6. Renal angiogram:- to access the vascularity.
Seldinger’s technique via transfemoral.
Pharmaco angiogram- tumour blush
Also therapeutic embolisation.
7. MRI/MR ANGIOGRAM:- Tumour thrombus in IVC
8. Chest x-ray:- cannon ball mets
9. Ct chest:-
10. Bone scan.
11. Peripheral smear, serum calcium, haematocrit and ESR
A, Magnetic resonance scan
of kidneys without
administration of
gadolinium suggests
anterior right renal mass.
B, After intravenous
administration of
gadolinium-labeled
diethylene-triamine-penta-
acetic acid, MRI shows
enhancement of this mass
indicative of malignancy.
Tissue Diagnosis
• Tissue diagnosis obtained from nephrectomy or
biopsy
Papillary (chromophilic) renal cell
carcinoma extending into the
collecting system with histological
findings
AJCC (AMERICAN JOINT COMMITTEE
ON CANCER STAGING): TNM STAGING
• TX:- PRIMARY TUMOUR CAN NOT BE ASSESSED
• T0:- NO PRIMARY TUMOUR.
• T1: <7CM limited to kidney
T1a: 0-4CM, T1b: 4-7cm
• T2: >7CM, limited to kidney.
• T3: T3a:- extends to adrenals, perinephric fat
(not gerota’s fascia).
T3b: entends into renal vein or IVC below
diaphragm.
T3c: extends into IVC above diaphragm.
• T4: invades Gerota’s fascia and extends beyond.
• N0:- no lymph nodes
• N1:- spread to single region of lymph nodes.
• N2:- spread to more than a group of lymph
nodes.
• M0:- no blood spread.
• M1:- distant spread, lungs 75%, soft tissue,
bones, liver, cns and skin
• Stage 1:- T1 N0 M0
• Stage 2:- T2 N0 M0
• Stage 3:- T1 or T2 N1 M0
T3 N0 or N1 M0
• Stage 4:- T4 anyN M0
AnyT anyN M1
Robson-Flock and Kadesky staging.
TREATMENT
SURGERY IS TREATMENT OF CHOICE!
1. Radical nephrectomy:-
• Structures removed?
• Approach:-Transperitoneal (common),
Others are retroperitoneal, Nagamatsu,
thoraco-abdominal and posterior
vertical.
• Position:- lateral
• Procedure: laporotomy
colon mobilised medially
vessels are identified, dissected and ligated (transfixation and
three ligatures proximally using silk or non absorbable sutures).
renal vein always first, why.? Problem?
preoperative renal artery embolisation can be done, why?, How?.
• IVC extension: Oblique vascular clamp placed, open, remove
tumour thrombus, suture.
• Supradiaphragmatic venacaval extension:- cardio- pulmonary
bypass.
Laparoscopic Radical Nephrectomy Hand-Assisted Laparoscopic
Radical Nephrectomy
2. Large fixed tumours:- palliative nephrectomy or debulking is
adviced, why?
3. Bilateral RCC: Bilateral partial nephrectomy is
done.
Renal artery is temporarily ocluded using
vascular clamps and kidney cooled, why?
Resected specimen send for frozen section
biopsy.
retained partial capsule is sutured after heamostasis
arterial clamp released.
A. Localized disease:
• Partial Nephrectomy(nephron-sparing surgery, NSS )
--polar tumor
--tumor size<4cm
--bilateral RCC
Laparoscopic NSS
Localized disease:
• Percutaneous/Laparoscopic Radiofrequency
Ablation or Cryoablation
• NO ROLE FOR RADIOTHERAPY!!!
• Chemotherapy: Vinblastine and progesterone
• Interferons and interleukins.
• Antiangiogenic drugs like endostatin and
angiostatin under trial.
• Humanised monoclonal antibodies like
bevacizumab under trial.
• Laporoscopic approach becoming popular.
Difference?
Prognosis
Factors:- 1. tumour size >4cm
2. entension into renal vein
3. presence of secondaries
4. local extension
5. hypercalcaemia and stauffer’s
syndrome.
5 years survival: stage 1 and 2 is 65%
stage 3 is 40%
stage 4 is 10%
THANK YOU

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RENAL CELL CARCINOMA

  • 2. NAME- Mr X AGE- 55 YEARS SEX- MALE ADDRESS- MANGALORE OCCUPATION- FACTORY WORKER PRESENTING COMPLAINTS  HEMATURIA  LOIN PAIN  MASS IN LOIN INSPECTION LOIN MASS PALPATION MOBILE,NODULAR, HARD,MOVES WITH RESPIRATION PERCUSSION DULL RENAL ANGLE
  • 3.
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.
  • 9. PATHOLOGY GROSS– UNILATERAL, UPPER POLE, LARGE ,GOLDEN YELLOW ,CIRCUMSCRIBED CUT SECTION - AREA OF NECROSIS,CYSTIC CHANGE, FOCI OF HAEMORRHAGE,THROMBUS
  • 10. CLEAR CELL TYPE INCIDENCE – 70% GENETICS – SPORADICS & FAMILIAL HISTOLOGY – CLEAR CYTOPLASM WELL DIFFERENTIATED INCIDENCE – 15% GENETICS -SPORADICS & FAMILIAL HISTOLOGY – PAPILLARY PATTERN PSAMMOMA BODIES PAPILLARY TYPE
  • 11. TYPE INCIDENCE GENETICS HISTOLOGY GRANULAR CELL TYPE 8% SPORADIC & FAMILIAL ABUNDANT ACIDOPHILIC CYTOPLASM MARKED ATYPIA CROMOPHOBE TYPE 5% MULTIPLE CROMOSOMES LOSS, HYPODIPLOIDY •MIXTURE PALE CLEAR CELL WITH PERINUCLEAR HALO •GRANULAR CELL SARCOMATOID TYPE 1.5% ------- WHORLS OF ATYPICAL ANAPLASTIC SPINDLE CELLS COLLECTING DUCT TYPE 0.5 TUBULAR & PAPILLARY PATTERN
  • 12. LYMPHATIC SPREAD PROLIFERATIVE TROMBUS EXTENDS INTO IVC CANNON BALL SECONDARIES IN LUNG VARICOCELE DUE TO BLOCKED LEFT RENAL VEIN BRAIN,BONE HILAR & PARA AORTIC LYMPHNODE PERINEPHRIC PAD OF FAT,CALYCES RENAL PELVIS
  • 14.
  • 15. Renal cell carcinoma (investigations, staging, treatment and prognosis).
  • 16. Investigations 1. Urine :- RBCs 2. IVU:- Shows mass lesion and irregular filling defect 3. U/S abdomen:- size, extension, lymph node, status of renal vein, spread to liver. 4. Ct scan:- Confirmatory status of renal vein and ivc lymph node status and tumour extension 5. CECT: Early lesions, function, spread and venous status. 6. Renal angiogram:- to access the vascularity. Seldinger’s technique via transfemoral. Pharmaco angiogram- tumour blush Also therapeutic embolisation. 7. MRI/MR ANGIOGRAM:- Tumour thrombus in IVC 8. Chest x-ray:- cannon ball mets 9. Ct chest:- 10. Bone scan. 11. Peripheral smear, serum calcium, haematocrit and ESR
  • 17.
  • 18. A, Magnetic resonance scan of kidneys without administration of gadolinium suggests anterior right renal mass. B, After intravenous administration of gadolinium-labeled diethylene-triamine-penta- acetic acid, MRI shows enhancement of this mass indicative of malignancy.
  • 19.
  • 20. Tissue Diagnosis • Tissue diagnosis obtained from nephrectomy or biopsy Papillary (chromophilic) renal cell carcinoma extending into the collecting system with histological findings
  • 21. AJCC (AMERICAN JOINT COMMITTEE ON CANCER STAGING): TNM STAGING • TX:- PRIMARY TUMOUR CAN NOT BE ASSESSED • T0:- NO PRIMARY TUMOUR. • T1: <7CM limited to kidney T1a: 0-4CM, T1b: 4-7cm • T2: >7CM, limited to kidney. • T3: T3a:- extends to adrenals, perinephric fat (not gerota’s fascia). T3b: entends into renal vein or IVC below diaphragm. T3c: extends into IVC above diaphragm. • T4: invades Gerota’s fascia and extends beyond.
  • 22. • N0:- no lymph nodes • N1:- spread to single region of lymph nodes. • N2:- spread to more than a group of lymph nodes. • M0:- no blood spread. • M1:- distant spread, lungs 75%, soft tissue, bones, liver, cns and skin
  • 23. • Stage 1:- T1 N0 M0 • Stage 2:- T2 N0 M0 • Stage 3:- T1 or T2 N1 M0 T3 N0 or N1 M0 • Stage 4:- T4 anyN M0 AnyT anyN M1
  • 25. TREATMENT SURGERY IS TREATMENT OF CHOICE! 1. Radical nephrectomy:- • Structures removed? • Approach:-Transperitoneal (common), Others are retroperitoneal, Nagamatsu, thoraco-abdominal and posterior vertical. • Position:- lateral
  • 26. • Procedure: laporotomy colon mobilised medially vessels are identified, dissected and ligated (transfixation and three ligatures proximally using silk or non absorbable sutures). renal vein always first, why.? Problem? preoperative renal artery embolisation can be done, why?, How?. • IVC extension: Oblique vascular clamp placed, open, remove tumour thrombus, suture. • Supradiaphragmatic venacaval extension:- cardio- pulmonary bypass.
  • 27. Laparoscopic Radical Nephrectomy Hand-Assisted Laparoscopic Radical Nephrectomy
  • 28. 2. Large fixed tumours:- palliative nephrectomy or debulking is adviced, why? 3. Bilateral RCC: Bilateral partial nephrectomy is done. Renal artery is temporarily ocluded using vascular clamps and kidney cooled, why? Resected specimen send for frozen section biopsy. retained partial capsule is sutured after heamostasis arterial clamp released.
  • 29. A. Localized disease: • Partial Nephrectomy(nephron-sparing surgery, NSS ) --polar tumor --tumor size<4cm --bilateral RCC Laparoscopic NSS
  • 30. Localized disease: • Percutaneous/Laparoscopic Radiofrequency Ablation or Cryoablation
  • 31. • NO ROLE FOR RADIOTHERAPY!!!
  • 32. • Chemotherapy: Vinblastine and progesterone • Interferons and interleukins. • Antiangiogenic drugs like endostatin and angiostatin under trial. • Humanised monoclonal antibodies like bevacizumab under trial. • Laporoscopic approach becoming popular. Difference?
  • 33. Prognosis Factors:- 1. tumour size >4cm 2. entension into renal vein 3. presence of secondaries 4. local extension 5. hypercalcaemia and stauffer’s syndrome. 5 years survival: stage 1 and 2 is 65% stage 3 is 40% stage 4 is 10%