Literature DB >> 11706439

Choroid plexus tumours: a surgically treated series.

M Barbosa1, O Rebelo, P Barbosa, A Lacerda, R Fernandes.   

Abstract

Choroid plexus tumours-carcinomas and papillomas are rare, especially in adults, and they pose some problems in their diagnosis and management. We have reviewed a series of nine cases from our institution surgically treated during the last 18 years. Their clinical charts, neuroradiological examinations, surgical technique, neuropathology and follow-up were analysed. In only one case total removal proved to be impossible, but even in cases of total removal recurrence appeared in two cases (one carcinoma and one papilloma). Morbility is especially associated with posterior fossa tumours. These rare tumours are managed surgically. They are usually associated with hydrocephalus, and it is difficult to forecast whether or not permanent CSF drainage will be required. A long-term follow-up is needed in patients with this type of tumour.

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Year:  2001        PMID: 11706439     DOI: 10.1016/s1130-1473(01)70712-9

Source DB:  PubMed          Journal:  Neurocirugia (Astur)        ISSN: 1130-1473            Impact factor:   0.553


  2 in total

1.  Embolization of a giant hypervascularized choroid plexus papilloma with onyx by direct puncture: a case report.

Authors:  Gustavo S Jung; Leonardo G Ruschel; Andre G Leal; Ricardo Ramina
Journal:  Childs Nerv Syst       Date:  2015-10-05       Impact factor: 1.475

2.  Treatment of choroid plexus tumors: a 20-year single institutional experience.

Authors:  Chetan Bettegowda; Owoicho Adogwa; Vivek Mehta; Kaisorn L Chaichana; Jon Weingart; Benjamin S Carson; George I Jallo; Edward S Ahn
Journal:  J Neurosurg Pediatr       Date:  2012-08-31       Impact factor: 2.375

  2 in total

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