Turkish Journal of Oncology Turkish Society for Radiation Oncology
Article Open Access Volume 23 · Issue 1 · 2008 pp. 020–025

Hemangiopericytoma: a case report

Ali Özcan BİNATLI1
1 Tepecik Eğitim ve Araştırma Hastanesi, Nöroşirürji Kliniği, İzmir, Turkey
2 Tepecik Eğitim ve Araştırma Hastanesi, Patoloji Bölümü, İzmir, Turkey
3 Ege Üniversitesi Tıp Fakültesi, Nöroşirürji Anabilim Dalı,İzmir, Turkey
Published: 2008 Pubmed: 75151 Article ID: 684
Abstract
Hemangiopericytoma is an uncommon neoplasm in central nervous system (CNS). Recently, it has been named under the classification of the spesific tumors of CNS in the meningioma family as the angioblastic variant by WHO in the years of 1997 and 2000. Surgery is very important for the successful treatment of these patients. Radiotherapy (RT) is helpful in the management after the operation. Because hemangiopericytomas are extremely difficult to cure surgicaly, patients should receive postoperative RT regardless of the amount of tumor resected. Guthrie et al. emphasized particularly the importance of complete tumor removal at the first operation and subsequent RT to prolong the survival period. In our case, 54- year-old male patient with Hemangiopericytoma was operated. The tumour has been totally resected and RT has been applied after the operation as it is mentioned above. The follow- up has been occuring sufficiently in our clinic.

Keywords: Hemangiopericytoma; meningeal neoplasms; radiotherapy; vimentin/analysis

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