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Turner syndrome and meningioma: support for a possible increased risk of neoplasia in Turner syndrome.
Pier, Danielle B; Nunes, Fabio P; Plotkin, Scott R; Stemmer-Rachamimov, Anat O; Kim, James C; Shih, Helen A; Brastianos, Priscilla; Lin, Angela E.
Afiliación
  • Pier DB; Medical Genetics Unit, MassGeneral Hospital for Children, Boston, MA, USA.
  • Nunes FP; Stephen E. & Catherine Pappas Center for Neuro-Oncology, Department of Neurology, Massachusetts General Hospital, Boston, MA, USA.
  • Plotkin SR; Stephen E. & Catherine Pappas Center for Neuro-Oncology, Department of Neurology, Massachusetts General Hospital, Boston, MA, USA; Department of Neurology, Massachusetts General Hospital, Boston, MA, USA.
  • Stemmer-Rachamimov AO; Department of Pathology, Massachusetts General Hospital, Boston, MA, USA.
  • Kim JC; Department of Pathology, Massachusetts General Hospital, Boston, MA, USA.
  • Shih HA; Department of Radiation Oncology, Massachusetts General Hospital, Boston, MA, USA.
  • Brastianos P; Department of Medicine, Massachusetts General Hospital, Boston, MA, USA; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Broad Institute of MIT and Harvard, Boston, MA, USA.
  • Lin AE; Medical Genetics Unit, MassGeneral Hospital for Children, Boston, MA, USA. Electronic address: lin.angela@mgh.harvard.edu.
Eur J Med Genet ; 57(6): 269-74, 2014.
Article en En | MEDLINE | ID: mdl-24675142
Neoplasia is uncommon in Turner syndrome, although there is some evidence that brain tumors are more common in Turner syndrome patients than in the general population. We describe a woman with Turner syndrome (45,X) with a meningioma, in whom a second neoplasia, basal cell carcinomas of the scalp and nose, developed five years later in the absence of therapeutic radiation. Together with 7 cases of Turner syndrome with meningioma from a population-based survey in the United Kingdom, and 3 other isolated cases in the literature, we review this small number of patients for evidence of risk factors related to Turner syndrome, such as associated structural anomalies or prior treatment. We performed histological and fluorescent in situ hybridization (FISH) of 22q (NF2 locus) analyses of the meningeal tumor to search for possible molecular determinants. We are not able to prove causation between these two entities, but suggest that neoplasia may be a rare associated medical problem in Turner syndrome. Additional case reports and extension of population-based studies are needed.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Turner / Neoplasias Meníngeas / Meningioma Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Adult / Female / Humans Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Turner / Neoplasias Meníngeas / Meningioma Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Adult / Female / Humans Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos