Renal Flashcards
1
Q
RCC
Localized Workup
10
A
- H&P
- Labs (CBC/ CMP/ LDH)
- UA
- CT A/P or MRI
- CT chest or CXR
- FH (genetic evaluation if indicated)
- Bone scan if indicated
- Brain MRI if indicated
- Ureteroscopy if indicated
- RMB if indicated
2
Q
RCC
Stage Ia Treatment
4
A
- Partial Nx (p)
- Radical Nx (select pts)
- Ablative techniques
- Active Surveillance
3
Q
RCC
Stage Ib Treatment
4
A
- Partial Nx
- Radical Nx
- Ablative techniques (select pts)
- Active Surveillance (select pts)
4
Q
RCC
Stage II Treatment
3
A
- Partial Nx
- Radical Nx
- Adjuvant pembrolizumab (Grade 4 ccRCC +/- sarcomatoid)
5
Q
RCC
Stage III Treatment
3
A
- Radical Nx
- Partial Nx (select pts)
- Adjuvant pembrolizumab (ccRCC)
6
Q
RCC
Stage IV (M0) Treatment
2
A
- Resectable: Radical Nx and adjuvant pembrolizumab if ccRCC
- Unresectable: First line systemic therapy
7
Q
RCC
Stage IV (M1) Treatment
2
A
- Resectable: Cytoreductive nephrectomy (select pts) or First line systemic therapy (consoder tissue sampling
- Tissue sampling and First-line systemic therapy
8
Q
RCC
First line Favorable ccRCC Systemic Therapy
8
A
- Axitinib + Pembrolizumab (p)
- Cabozantinib + Nivolumab (p)
- Lenvatinib + Pembrolizumab (p)
- Ipilimumab + Nivolumab (p)
- Axitinib + Avelumab
- Cabozantinib
- Pazopanib
- Sunitinib
9
Q
RCC
First line Int/ Poor ccRCC Systemic Therapy
8
A
- Axitinib + Pembrolizumab (p)
- Cabozantinib + Nivolumab (p)
- Ipilimumab + Nivolumab (p)
- Lenvatinib + Pembrolizumab (p)
- Cabozantinib (p)
- Axitinib + Avelumab
- Pazopanib
- Sunitinib
10
Q
RCC
Bosniak 1
7
A
- Homogeneous
- Smooth thin wall (less than 2mm)
- No septa
- No calcification
- No enhancement
- -9 - 20 HU
- 1.7% malignant
11
Q
RCC
Bosniak 2
8
A
- Homogeneous hyperdense and less than 3cm
- Smooth thin wall (less 2mm)
- Few enhancing septa (1-3)
- Small calcifications
- Non contrast - 9 to 20HU or over 70HU
- Contrast nonenhancing masses over 20 HU
- Contrast enhancing less than 30
- Homogeneous low attenuation masses that are too small too characterize
12
Q
RCC
Bosniak 2F
7
A
- Homogeneous
- Smooth 3mm enhancing wall
- Smooth 3mm enhancing septa
- More than 4 smooth thin (<2mm) enhancing septa
- Few calcifications
- Hyperdense cyst greater than 3cm
- 18.5% malignant
13
Q
RCC
Bosniak 3
3
A
- Enhancing irregular walls or septa
- One or more thick (>4mm) enhancing septa
- 33% malignant
14
Q
RCC
Bosniak 4
4
A
- Thickened or irregular walls
- Enhancing soft tissue components
- Measurable contrast enhancement
- 92.5% malignant
15
Q
RCC
Hereditary RCC Syndromes
7
A
- Von Hipple-Lindau
- Hereditary Papillary Renal Carcinoma
- Birt-Hogg-Dube Syndrome
- Tuberous Sclerosis Complex
- Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC)
- BAP1 tumor predisposition syndrome
- Hereditary paraganglioma/ Pheochromocytoma syndrome (PGL/PCC)
16
Q
RCC
Common RCC Pathology
7
A
- Clear cell RCC
- Papillary RCC type 1 and 2
- Chromophobe
- Collecting Duct (Bellini) carcinoma
- Medullary Renal carcinoma
- Hereditary leiomyomatosis associated RCC (FH-deficient RCC)
- Succinate dehydrogenase-deficient RCC
17
Q
RCC
von Hippel-Lindau
5
A
- Clear cell
- Autosomal dominant
- Hemangioblastomas of retina, spine and brain (less common)
- Pheochromocytoma
- Treat with Belzutifan
18
Q
RCC
Tuberous Sclerosis
6
A
- Autosomal Dominant
- LG Oncocytic tumor /Chromophobe RCC
- Renal AMLs
- Subependymal nodules
- Shagreen patch
- Treat with Everolimus
19
Q
RCC
Birt-Hogg-Dube
5
A
- Chromophobe/ Oncocytomas /Hybrid Oncocytic tumors
- Clear cell RCC
- Angiomyolipomas
- Papillary RCC
- Spontaneoous pneumothorax and pulmonary cysts
20
Q
RCC
Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC)
4
A
- Autosomal Dominant
- FH-deficient RCC
- Leiomyomas of skin and uterus
- PET-positive adrenal adenomas
21
Q
RCC
Hereditary papillary renal carcinoma (HPRC)
4
A
- Papillary RCC
- Autosomal Dominant
- Multifocal bilateral renal cell tumors
- Treat with Erlotinib + Bevacizumab
22
Q
RCC
BAP1 tumor predisposition syndrome
4
A
- Clear cell
- Autosomal dominant
- Melanoma (uveal and cutaneous)
- Mesothelioma
23
Q
RCC
Hereditary paraganglioma/ pheochromocytoma syndrome (PGL/PCC)
5
A
- SDH-deficient RCC
- Autosomal dominant
- Head and neck PGL
- Adrenal and extra-adrenal PCCs
- Gastrointstinal stromal tumors (GIST)
24
Q
RCC
Malignancy based on size
3
A
- 46% of masses less than 1cm are benign
- 40% of masses less than 2cm are benign
- 20-30% of masses less than 4cm are benign