| Literature DB >> 28695322 |
Francesco Massari1, Chiara Ciccarese2, Ondrej Hes3, Michal Michal3, Anna Caliò4, Michelangelo Fiorentino5, Francesca Giunchi5, Alessandro D'Amuri6, Francesca Sanguedolce7, Roberto Sabbatini8, Annalisa Guida8, Andrea Ardizzoni1, Camillo Porta9, Roberto Iacovelli2, Giampaolo Tortora2, Luca Cima4, Cinzia Ortega10, Alberto Lapini11, Guido Martignoni4,12, Matteo Brunelli13.
Abstract
The new WHO 2016 classification of renal neoplasia encounters the new entity called "clear cell papillary renal cell carcinoma" (ccpRCC). The ccpRCC has been long included as a subtype of clear cell RCC histotype and it actually ranges from 2 to 9% in different routinely available cohort of renal carcinomas. Of important note, ccpRCC does not show any recurrences or metastases or lymph-node invasion and the outcome is always good. We reviewed twenty-four publications with available follow-up for patients (no. 362) affected by clear cell papillary RCCs/renal adenomatoid tumours and notably ccpRCC harbors an indolent clinical behavior after a mean of 38 months (3,5 years) of follow-up. This paper reviews the histological, molecular and clinical features characterizing ccpRCC, with the goal of focusing the knowledge of the benign fashion of this new tumour entity, supporting the idea of a new renal cell adenoma recruited morphologically from ex conventional clear cell RCC tumours.Entities:
Keywords: Benign; Clear cell papillary RCC; Renal adenoma; Renal adenomatoid tumour (RAT); WHO 2016 classification of renal neoplasia
Mesh:
Year: 2017 PMID: 28695322 DOI: 10.1007/s12253-017-0271-x
Source DB: PubMed Journal: Pathol Oncol Res ISSN: 1219-4956 Impact factor: 3.201