Characteristics and Outcome of Children with Renal Cell Carcinoma: A Narrative Review.

outcome pediatric renal cell carcinoma survival treatment

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
03 Jul 2020
Historique:
received: 02 06 2020
revised: 30 06 2020
accepted: 01 07 2020
entrez: 9 7 2020
pubmed: 9 7 2020
medline: 9 7 2020
Statut: epublish

Résumé

Pediatric renal cell carcinoma (RCC) is a rare type of kidney cancer, most commonly occurring in teenagers and young adolescents. Few relatively large series of pediatric RCC have been reported. Knowledge of clinical characteristics, outcome and treatment strategies are often based on the more frequently occurring adult types of RCC. However, published pediatric data suggest that clinical, molecular and histological characteristics of pediatric RCC differ from adult RCC. This paper summarizes reported series consisting of ≥10 RCC pediatric patients in order to create an up-to-date overview of the clinical and histopathological characteristics, treatment and outcome of pediatric RCC patients.

Identifiants

pubmed: 32635225
pii: cancers12071776
doi: 10.3390/cancers12071776
pmc: PMC7407101
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : Stichting Kinderen Kankervrij
ID : 341

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Auteurs

Justine N van der Beek (JN)

Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Department of Radiology and Nuclear Medicine, University Medical Center Utrecht/Wilhelmina Children's Hospital, Utrecht University, 3584 CX Utrecht, The Netherlands.

James I Geller (JI)

Division of Oncology, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH 45229, USA.

Ronald R de Krijger (RR)

Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Department of Pathology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.

Norbert Graf (N)

Department of Pediatric Oncology & Hematology, Saarland University Medical Center and Saarland University Faculty of Medicine, D-66421 Homburg, Germany.

Kathy Pritchard-Jones (K)

UCL Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.

Jarno Drost (J)

Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Oncode Institute, 3521 AL Utrecht, The Netherlands.

Arnauld C Verschuur (AC)

Department of Pediatric Oncology, Hôpital d'Enfants de la Timone, APHM, 13005 Marseille, France.

Dermot Murphy (D)

Department of Paediatric Oncology, Royal Hospital for Children, Glasgow G51 4TF, Scotland, UK.

Satyajit Ray (S)

Department of Paediatric Oncology, Royal Hospital for Children, Glasgow G51 4TF, Scotland, UK.

Filippo Spreafico (F)

Pediatric Oncology Unit, Department of Medical Oncology and Hematology, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 Milano, Italy.

Kristina Dzhuma (K)

UCL Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.

Annemieke S Littooij (AS)

Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Department of Radiology and Nuclear Medicine, University Medical Center Utrecht/Wilhelmina Children's Hospital, Utrecht University, 3584 CX Utrecht, The Netherlands.

Barbara Selle (B)

Department of Pediatric Hematology and Oncology, St. Annastift Children's Hospital, 67065 Ludwigshafen, Germany.

Godelieve A M Tytgat (GAM)

Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.

Marry M van den Heuvel-Eibrink (MM)

Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.

Classifications MeSH