Embryonal Tumor With Abundant Neuropil and True Rosettes-Reference-Cited by-同舟云学术

Embryonal Tumor With Abundant Neuropil and True Rosettes

Published:2013-01-17 Issue:12 Volume:28 Page:1709-1715
ISSN:0883-0738
Container-title:Journal of Child Neurology
language:en
Short-container-title:J Child Neurol

Author:

Alexiou George A.¹,Stefanaki Kalliopi²,Vartholomatos George³,Sfakianos George¹,Prodromou Neofytos¹,Moschovi Maria⁴

Affiliation:

1. Department of Neurosurgery, Children’s Hospital “Agia Sofia,” Athens, Greece

2. Department of Pathology, Children’s Hospital “Agia Sofia,” Athens, Greece

3. Haematology Laboratory, Unit of Molecular Biology, University Hospital of Ioannina, Ioannina, Greece

4. Hematology Oncology Unit of 1st Department of Pediatrics of Athens University, Athens, Greece

Abstract

Embryonal tumor with abundant neuropil and true rosettes has been recently defined as a distinct central nervous system embryonal neoplasm, although it was initially regarded as a subtype of central nervous system primitive neuroectodermal tumor. To date 70 cases have been reported. We have performed a literature review and we present 2 new cases. Analysis of the reported data revealed that radiotherapy, tumor excision and high-dose adjuvant chemotherapy with sequential autologous hematopoietic stem cell rescue have a prognostic significance.

Publisher

SAGE Publications

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.1177/0883073812471434

Reference24 articles.

1. Pediatric Neuroblastic Brain Tumors Containing Abundant Neuropil and True Rosettes

2. Analysis of Chromosome 19q13.42 Amplification in Embryonal Brain Tumors with Ependymoblastic Multilayered Rosettes

3. Embryonal tumor with abundant neuropil and true rosettes: a report of three cases of a rare tumor, with an unusual case showing rhabdomyoblastic and melanocytic differentiation

4. Embryonal tumor with abundant neuropil and true rosettes (ETANTR) with loss of morphological but retained genetic key features during progression

5. Sudden paraplegia in a case of apparently isolated frontal embryonal tumour with abundant neuropil and true rosettes

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