Literature DB >> 25442925

Congenital multifocal rhabdoid tumor: a case with peculiar biological behavior and different response to treatment according to location (central nervous system and kidney).

Luca Pio1, Claudia Milanaccio2, Samantha Mascelli2, Alessandro Raso2, Paolo Nozza2, Angela R Sementa2, Armando Cama2, Piero Buffa2, Stefano Avanzini2, Marianna Vannati1, Valeria Capra2, Edoardo Lanino2, Andrea Rossi2, Giovanni Morana2, Gian M Magnano2, Mariasavina Severino2, Maria L Garrè3.   

Abstract

Atypical teratoid/rhabdoid tumor (AT/RT) of the central nervous system and malignant rhabdoid tumor of the kidney (MRTK) may present with different responses to chemotherapy and outcomes. We describe the case of an infant with multifocal rhabdoid tumor with different behavior and response to treatment, depending on the anatomic site.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  AT/RT; MRTK; Rhabdoid tumor

Mesh：

Substances：

Year:  2014        PMID： 25442925     DOI： 10.1016/j.cancergen.2014.08.003

Source DB:  PubMed          Journal:  Cancer Genet


  2 in total

1.  Multifocal atypical teratoid/rhabdoid tumor: a rare entity.

Authors:  Mohammad Sadegh Masoudi; Nima Derakhshan; Fariborz Ghaffarpasand; Bita Geramizadeh; Mina Heydari
Journal:  Childs Nerv Syst       Date:  2016-10-18       Impact factor: 1.475

2.  Melanotic Neuroectodermal Tumor of Infancy (MNTI) and Pineal Anlage Tumor (PAT) Harbor A Medulloblastoma Signature by DNA Methylation Profiling.

Authors:  Oscar Lopez-Nunez; Rita Alaggio; Ivy John; Andrea Ciolfi; Lucia Pedace; Angela Mastronuzzi; Francesca Gianno; Felice Giangaspero; Sabrina Rossi; Vittoria Donofrio; Giuseppe Cinalli; Lea F Surrey; Marco Tartaglia; Franco Locatelli; Evelina Miele
Journal:  Cancers (Basel)       Date:  2021-02-09       Impact factor: 6.639
  2 in total

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