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Verfasst von:Gubian, Arthur [VerfasserIn]   i
Titel:Intracranial solitary fibrous tumors
Titelzusatz:a heterogeneous entity with an uncertain clinical behavior
Verf.angabe:Arthur Gubian, Mario Ganau, Helene Cebula, Julien Todeschi, Antonino Scibilia, Georges Noel, Giorgio Spatola, Dominique Chaussemy, Beniamino Nannavecchia, Paolo Gallinaro, Andres Coca, Raoul Pop, Francesco Signorelli, Francois Proust, Benoit Lhermitte, Salvatore Chibbaro
E-Jahr:2019
Jahr:1 February 2019
Umfang:9 S.
Fussnoten:Gesehen am 19.09.2019
Titel Quelle:Enthalten in: World neurosurgery
Ort Quelle:Amsterdam : Elsevier, 2010
Jahr Quelle:2019
Band/Heft Quelle:126(2019), Seite e48-e56
ISSN Quelle:1878-8769
Abstract:Background - Intracranial solitary fibrous tumors (ISFTs) are rare mesenchymal neoplasms originating in the meninges and characterized by very different biologic and clinical behaviors. Benign histotypes, such as hemangiopericytomas, are now considered a cellular phenotypic variant of this heterogeneous group of rare spindle-cell tumors. Owing to their rarity and resemblance to other, more common brain tumors, ISFTs are often poorly recognized and remain a diagnostic challenge. - Methods - We describe a surgical series of 29 patients treated for ISFTs confirmed histologically and through immunohistochemistry. We attempt to provide a focus on the natural history of these pathologies and the need for tailored management. - Results - This was a retrospective consecutive series of 29 patients with either solitary fibrous tumor (n = 14) or hemangiopericytoma (n = 15) over a 10-year period. Mean follow-up time was 37.71 months. Recurrence rate was 42.9% for solitary fibrous tumors versus 26.7% for hemangiopericytomas. STAT6 expression was 66.7% in hemangiopericytomas versus 42.9% in SFTs. - Conclusions - Histopathology and immunohistochemical staining (characterized by positive expression of mainly STAT6 but also CD34, Bcl-2 protein, and vimentin) are key in diagnosis and management of ISFTs. Although ISFTs are still considered benign lesions with very rare aggressive evolution, their clinical behavior is largely unpredictable. This study highlights the importance of relying on immunohistochemistry for a thorough definition of the management strategy.
DOI:doi:10.1016/j.wneu.2019.01.142
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1016/j.wneu.2019.01.142
 Volltext: http://www.sciencedirect.com/science/article/pii/S1878875019302426
 DOI: https://doi.org/10.1016/j.wneu.2019.01.142
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Anaplasia
 Hemangiopericytoma
 Intracranial solitary fibrous tumors
 Radiotherapy
 Recurrence
K10plus-PPN:1677363177
Verknüpfungen:→ Zeitschrift

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