Giant cell tumors of the clivus: Case report and literature review

Surg Neurol Int. 2015 Nov 25;6(Suppl 25):S623-7. doi: 10.4103/2152-7806.170459. eCollection 2015.

Abstract

Background: Clival giant cell tumors (GCTs) are extremely rare with only eight cases reported to date, and malignant transformation is quite rare. Herein, we report a case of an uncontrolled clival GCT, which was transformed malignant, and review the literature.

Case description: A 25-year-old man experienced double vision for 1 month. Computed tomography and magnetic resonance imaging revealed a clival tumor. The endonasal endoscopic transsphenoidal approach (EEA) was used, and partial resection was performed because of massive bleeding. Histological examination showed a GCT. After radiation therapy, the tumor recurred; the EEA and the anterior transpetrosal approaches were used to perform second and third operations, respectively. The MIB-1 index increased from 4.2% to 26.3%.

Conclusions: GCTs are difficult to treat because of their location, vascularity, and the potential for malignant transformation.

Keywords: Clivus; giant cell tumor; malignant transformation.