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KIDNEY TUMORS
PAPILLARY RCC
Subclassification into type 1 and type 2 is no longer recommended.
PRCC has classic morphology historically in type 1 category.
Criteria of foamy histiocytes and psammoma bodies is not required.
Many tumors previously diagnosed as type 2 PRCC now constitute independent entities
 Positive for AMACR, Vimentin, CD10
PAPILLARY RCC
Arising from Renal cortex
Low grade tumors RET mutation
High grade tumors CDKN2A
Prognosis favourable
CLASSIFICATION OF PAEDIATRIC RENAL TUMORS
OSSIFYING RENAL OF INFANCY
CONGENITAL MESOBLASTIC NEPHROMA
RHABDOID TUMOR OF KIDNEY
CLEAR CELL SARCOMA OF KIDNEY
CLEAR CELL SARCOMA KIDNEY
A/K/A Bone metastasizing renal tumor of childhood.
BCOR mutations or YWHAE:NUTM2 gene fusion.
Centred in the renal medulla.
MC age group is less than 3yrs.
CLEAR CELL SARCOMA KIDNEY
Gross- Homogenous, lobular with light pink soft areas.
Many histological patterns.
Ovoid tumour cells with nuclear and/or cytoplasmic clearing at least focally, distinctive
arborizing fibrovascular septa
ADULT CYSTIC NEPHROMA
A/K/A Multilocular cystic nephroma.
Benign neoplasm in adult
Women> Men
Hormonal imbalance
ADULT CYSTIC NEPHROMA
Well circumscribed globular mass with fibrous capsule.
Multiple non communicating cysts without any solid areas.
M/E cyst wall lined by cuboidal or flattened epithelium with clear cytoplasm resembling ovarian
stroma.
PAEDIATRIC CYSTIC NEPHROMA
Almost exclusively occurs in children with higher prevalence in males
Similar macroscopic and microscopic findings
Most harbor DICER1 mutations.
MEST
MIXED EPITHELIALAND STROMAL TUMOR
Comprises of solid and cystic or completely solid areas.
The epithelial component is usually scattered in the stroma or closely clustered. Small cysts
containing eosinophilic material reminiscent of thyroid follicles, complex branching tubules,
phyllodes-type architecture, and papillary structures have been seen.
WILMS TUMOR
Nephroblastoma is a malignant embryonal neoplasm derived
from nephrogenic blastemal cells that replicates the histology
of developing kidneys and often shows divergent patterns of
differentiation.

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NEW ENTITIES IN KIDNEY TUMORS in PPT format.pptx

  • 2.
  • 3.
  • 4.
  • 5. PAPILLARY RCC Subclassification into type 1 and type 2 is no longer recommended. PRCC has classic morphology historically in type 1 category. Criteria of foamy histiocytes and psammoma bodies is not required. Many tumors previously diagnosed as type 2 PRCC now constitute independent entities  Positive for AMACR, Vimentin, CD10
  • 6. PAPILLARY RCC Arising from Renal cortex Low grade tumors RET mutation High grade tumors CDKN2A Prognosis favourable
  • 7.
  • 8. CLASSIFICATION OF PAEDIATRIC RENAL TUMORS OSSIFYING RENAL OF INFANCY CONGENITAL MESOBLASTIC NEPHROMA RHABDOID TUMOR OF KIDNEY CLEAR CELL SARCOMA OF KIDNEY
  • 9.
  • 10. CLEAR CELL SARCOMA KIDNEY A/K/A Bone metastasizing renal tumor of childhood. BCOR mutations or YWHAE:NUTM2 gene fusion. Centred in the renal medulla. MC age group is less than 3yrs.
  • 11. CLEAR CELL SARCOMA KIDNEY Gross- Homogenous, lobular with light pink soft areas. Many histological patterns. Ovoid tumour cells with nuclear and/or cytoplasmic clearing at least focally, distinctive arborizing fibrovascular septa
  • 12.
  • 13. ADULT CYSTIC NEPHROMA A/K/A Multilocular cystic nephroma. Benign neoplasm in adult Women> Men Hormonal imbalance
  • 14. ADULT CYSTIC NEPHROMA Well circumscribed globular mass with fibrous capsule. Multiple non communicating cysts without any solid areas. M/E cyst wall lined by cuboidal or flattened epithelium with clear cytoplasm resembling ovarian stroma.
  • 15.
  • 16. PAEDIATRIC CYSTIC NEPHROMA Almost exclusively occurs in children with higher prevalence in males Similar macroscopic and microscopic findings Most harbor DICER1 mutations.
  • 17. MEST MIXED EPITHELIALAND STROMAL TUMOR Comprises of solid and cystic or completely solid areas. The epithelial component is usually scattered in the stroma or closely clustered. Small cysts containing eosinophilic material reminiscent of thyroid follicles, complex branching tubules, phyllodes-type architecture, and papillary structures have been seen.
  • 18. WILMS TUMOR Nephroblastoma is a malignant embryonal neoplasm derived from nephrogenic blastemal cells that replicates the histology of developing kidneys and often shows divergent patterns of differentiation.