Papillary renal cell carcinoma
Also known as chromophil carcinoma, it represents a minority of renal cell carcinomas. It can be hereditary or sporadic. The sporadic papillary renal cell carcinoma is characterized by trisomy of chromosomes 7, 16, and 17, and loss of chromosome Y. The peak incidence is in the sixth and seven decades. It is classified as type 1 or 2, based on the cytoplasmic volume and the thickness of the lining neoplastic cells. The prognosis is more favorable than for conventional (clear cell) renal cell carcinoma. -- 2003
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20 Years of Teaching To Both UGs & PGs
As Assistant, Associate & Professor
Gandhi Medical College, Dr. NTRUHS
MD Pathology
Ram Manohar Lohia Hospital
Senior Resident
National Institute of Pathology, ICMR
DNB Pathology
Hope International Hospital
Consultant Pathologist
Rangaraya Medical College
M.D
Anand Hospital
Neuro Intensive Care
Zhengzhou University
MBBS
Dr. Richa Physiotherapy and Rehabilitation Clinic
HOD
AIIMS
MPT
Prendas Jalaram and Vallabha Harya and Org Acneilson Marg
Psyhologist
Baroda Medical Collage
Md path
KBNIMS
Mbbs
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