Literature DB >> 12806512

[Meningioma with rhabdoid transformation: case report].

Leodante Batista da Costa1, Josaphat Vilela de Morais.   

Abstract

Meningiomas represent aproximatelly 30% of all intracranial tumors in autopsy studies. With an incidence of 2.3 per 100000, they are considered commom tumors in clinical practice. Twenty percent of the all intracranial tumors diagnosed in vivo are meningiomas. Most of these lesions are benign and the prognosis is intimatelly related to acessibility and ressectability of the lesion. Malignant meningiomas are rare lesions, representing between 1 to 11% of all meningiomas, varying with the definition of pathological criteria for malignancy used, and are categorized in atypical or malignant. Only recently rhabdoid transformation of meningiomas have been reported. We present a case of an extremelly aggressive rhabdoid meningioma in a 56 year-old woman. The tumor was surgically removed twice, with a lethal outcome due to local recurrence, despite maximum radiation and quimiotherapy, six months after the initial presentation.

Entities:  

Mesh:

Year:  2003        PMID: 12806512     DOI: 10.1590/s0004-282x2003000200023

Source DB:  PubMed          Journal:  Arq Neuropsiquiatr        ISSN: 0004-282X            Impact factor:   1.420


  2 in total

1.  Rhabdoid meningioma: a new subtype of malignant meningioma also apt to occur in children.

Authors:  Juan F Martínez-Lage; Belén Ferri Niguez; Joaquín Sola; Miguel A Pérez-Espejo; Javier Ros de San Pedro; Víctor Fernandez-Cornejo
Journal:  Childs Nerv Syst       Date:  2005-03-31       Impact factor: 1.475

2.  Primary calcified rhabdoid meningioma of the cranio-cervical junction: A case report and review of literature.

Authors:  Mohammad Abolfotoh; Daryoush Tavanaiepour; Changki Hong; Ian F Dunn; Hart Lidov; Ossama Al-Mefty
Journal:  J Craniovertebr Junction Spine       Date:  2012-01
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.