Hayashi S, Kurihara H, Hirato J, Sasaki T
Department of Neurosurgery, Gunma University School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma 371-8511, Japan.
Neurosurgery. 2001 Nov;49(5):1241-5. doi: 10.1097/00006123-200111000-00042.
Solitary fibrous tumors (SFTs) are rare tumors of mesenchymal origin that typically arise in the pleura. Only 24 cases of SFTs in the orbit have been reported, all located within the orbit and generally with a benign course. We report the first case of an orbital SFT with extraorbital extension and short-term regrowth.
A 54-year-old man presented with proptosis and double vision that had persisted for 7 months. The tumor extended from the right extraconal inferolateral orbit to the extradural middle cranial fossa and cavernous sinus, via the superior orbital fissure, on magnetic resonance imaging scans. Positron emission tomography with [(18)F]fluorodeoxyglucose demonstrated faint uptake in the orbital portion.
Resection of the tumor was performed twice, because of short-term regrowth of the residual tumor in the orbit. The histological diagnosis was a SFT. The MIB-1 labeling index was 7% and the mitotic count was 5 mitotic figures/10 high-power fields at the time of the second operation. These findings indicate the malignant nature of the tumor.
The natural history of SFTs of the orbit remains unclear, and the importance of careful and continued follow-up monitoring of the tumor should be emphasized.
孤立性纤维瘤(SFTs)是一种罕见的间叶源性肿瘤,通常起源于胸膜。眼眶内的SFTs仅报道过24例,均位于眼眶内,且一般病程呈良性。我们报告首例眼眶SFT伴有眶外扩展及短期复发。
一名54岁男性,出现眼球突出和复视7个月。磁共振成像扫描显示,肿瘤从右侧眶锥外下侧延伸至硬膜外中颅窝及海绵窦,经眶上裂。[18F]氟脱氧葡萄糖正电子发射断层扫描显示眼眶部分有轻微摄取。
由于眼眶内残留肿瘤短期复发,进行了两次肿瘤切除术。组织学诊断为SFT。第二次手术时,MIB-1标记指数为7%,有丝分裂计数为每10个高倍视野5个有丝分裂象。这些结果表明肿瘤具有恶性特征。
眼眶SFTs的自然病程仍不清楚,应强调对肿瘤进行仔细和持续随访监测的重要性。