| Literature DB >> 19652916 |
María Sol Brassesco1, Elvis Terci Valera, Aline Paixão Becker, Angel Mauricio Castro-Gamero, André de Aboim Machado, Antônio Carlos Santos, Carlos Alberto Scrideli, Ricardo Santos Oliveira, Hélio Rubens Machado, Luiz Gonzaga Tone.
Abstract
Encephalocutaneous lipomatosis (ECCL), or Haberland syndrome, is an uncommon congenital disorder with unique cutaneous, ocular and neurological features. In the present article, we describe a 3-year-old boy with ECCL who developed an extensive and recurring intraventricular low-grade glioma with atypical pathological features and elevated mitotic index. Cytogenetic analysis from tumor sample was also performed. This is the first report of a low-grade astrocytoma occurring in a child with ECCL. Whether or not the origin of the tumor is associated to the pathogenesis of the underlying syndrome is a matter for further investigation.Entities:
Mesh:
Year: 2009 PMID: 19652916 DOI: 10.1007/s11060-009-9978-1
Source DB: PubMed Journal: J Neurooncol ISSN: 0167-594X Impact factor: 4.130