WHAT IS RENAL CELL
CARCIMONA (RCC)?
Cancer arising from
the lining of proximal
convoluted tubule.
The most common
type of kidney cancer.
Also known as Renal
Adenocarcinomaor
Grawitz'sTumor.
Most lethal of all the
genitourinary tumors.
HOW DO YOU CLASSIFY
RCC?
Clear cell renal cell carcinoma.
Papillary renal cell carcinoma.
Chromophoberenal cell carcinoma.
Collecting duct carcinoma.
Chromophob
e
Clear Cell Papillary
EPIDIMOLOGY OF RCC
The incidence of renal cell carcinoma is
rising steadily.
More common in men than women,
male to female ratio is 1.6:1.
Blacks at an higher risk than whites.
WHAT LEADS TO RCC?
Cigarette smoking.
Obesity.
Hypertension.
Family history of the disease.
Patients with inherited diseases like von
HippelLindaudisease.
Hysterectomy is associated with
doubled risk.
Dialysis patients with acquired cystic
disease of kidney show greater risk.
PATHOLOGY
The gross and microscopic
appearance is highly variable.
May present as reddened
areas where blood vessels
have bled and cysts
containing watery fluids.
Litemicroscopy shows tumor
cells forming cords, papillae,
tubules or nests.
RCC cells may be clear,
granular, mixed clear and
granular or sarcomoidand
spindle.
Most of the tumors are mixed
and they are most
aggressive.
SIGNS AND SYMPTOMS
Classic triad of : Hematuria,,
Flank pain
Abdominal mass
Signs may include:
Malaise,weightloss and anorexia
Abnormal urine color
Polycythemia
Anemia
Fracture of hip
Varicocele.enlargementof testicle on left side
Pallor or plethora
Hirsutism
Constipation
Hypertension
Hypercalcemia
Leg and ankle swelling
STAGING
Based on examination,imagingand biopsy
AJCC (TNM) staging system:
T categories for kidney cancer:
T0: No evidence of primary tumor
T1: The tumor is only in the kidney and is 7cm or less across
T1a: The tumor is 4cm across or smaller
T1b: The tumor is larger than 4cm but not larger than 7cm
T2: The tumor is larger than 7cm across but is still in the kidney
T2a: The tumor is more than 7cm but not more than 10
T2b: The tumor is more than 10cm across
T3: The tumor is growing into a major vein or tissue around the
kidney but not into adrenals or beyond Gerota,sfascia
T3a: The tumor is growing into the main vein or into fatty
tissue around the kidney
T3b: The tumor is growing into the venacavaleading into
the heart
T3c: The tumor has grown into the part of venacavathat is
within the chest or growing into the wall of that blood
vessel
T4: The tumor has spread beyond Gerota,sfascia. It may have
grown into the adrenal gland
STAGING (CONTINUED)
STAGING (CONTINUED)
N categories for kidney cancer:
N0: No spread to nearby lymph nodes
N1: tumor has spread to nearby lymph
nodes
M categories for kidney cancer:
M0: There is no spread to distant lymph
nodes or other organs
M1: Distant metastasis is present
,distant lymph nodes and to organs like
lungs, bone, brain and liver
HOW TO TREAT RCC?
If only in kidneys, it can be cured 90% of the time with
surgery.
If it has spread outside the kidneys into the nodes or the
main vein, it must be treated with cytoreductivesurgery.
RRC is resistant to chemo and radiotherapy in most
cases
May respond to immunotherapy
PARTIAL NEPHRECTOMY:
For treating small renal tumors(< 4cm)
Bilateral renal cell carcinoma
It can be done via laproscopictechniques
RADICAL NEPHRECTOMY:
Surgical removal of kidney along with adrenal gland,
retroperitoneal lymphnodes, perinephricfat and Gerota's
fascia
In cases where the tumor has spread into the renal vein,
IVC and right atrium, this portion of tumor can be
surgically removed as well.
Medications like tyrosine kinaseinhibitors including
nexavarand rapamycinhave shown to improve the
PROGNOSIS
For tumors less than 4cm 5 year survival
rate is 90-95%
For larger tumors confined to kidneys
without venous invasion survival is 80-85%
For tumors that extend through the renal
capsule n local fascia survivability reduces
to near 60%
For metastasis to lymph nodes survival
rate is around 5-15%
For spread to other organs 5 year survival
rate is less than 5%