Low-grade astrocytoma in a child with encephalocraniocutaneous lipomatosis


Autoria(s): BRASSESCO, Maria Sol; VALERA, Elvis Terci; BECKER, Aline Paixao; CASTRO-GAMERO, Angel Mauricio; MACHADO, Andre de Aboim; SANTOS, Antonio Carlos; SCRIDELI, Carlos Alberto; OLIVEIRA, Ricardo Santos; MACHADO, Helio Rubens; TONE, Luiz Gonzaga
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

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.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[07/54236-4]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[06/04827-3]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[07/04065-9]

Identificador

JOURNAL OF NEURO-ONCOLOGY, v.96, n.3, p.437-441, 2010

0167-594X

http://producao.usp.br/handle/BDPI/25115

10.1007/s11060-009-9978-1

http://dx.doi.org/10.1007/s11060-009-9978-1

Idioma(s)

eng

Publicador

SPRINGER

Relação

Journal of Neuro-oncology

Direitos

restrictedAccess

Copyright SPRINGER

Palavras-Chave #Astrocytoma #Brain tumor #Childhood cancer #ECCL #Genetic disorder #PILOCYTIC ASTROCYTOMAS #BRAIN-TUMORS #ABNORMALITIES #CYTOGENETICS #GENE #Oncology #Clinical Neurology
Tipo

article

original article

publishedVersion