Lanuza A, Lazaro R, Salvador M, Solanes C, Ramos F, Sorli E
Department of Ophthalmology, General Hospital of Castellon, Spain.
Int Ophthalmol. 1998;22(5):265-8. doi: 10.1023/a:1006365730475.
Solitary fibrous tumour (SFT) of the orbit is a very rare lesion that may be misdiagnosed as fibrous histiocytoma, haemangiopericytoma, or other orbital tumour. We studied a case of SFT of the orbit in a 35-year-old woman.
The patient, with a 1-year history, reported a 'pressure' sensation behind her right eye, but no pain, vision changes, or other associated symptoms. Ocular examination was normal. Magnetic resonance imaging (MRI) showed a well-circumscribed medial mass in the right orbit. The tumour was excised.
The tumour was a cellular spindle-cell neoplasm with a storiform pattern. The tumour cells were spindle-shaped with bland nuclei and rare mitoses. Immunostaining was positive for vimentin and CD34, but negative for cytokeratin (AE1-AE3), EMA, desmin, smooth muscle actin, S-100, CD31, CD45 and bcl-2.
SFT can infrequently involve the orbit. The tumour must be removed entirely to avoid recurrences. Careful and continued follow-up is important because orbital recurrence may occur several years after the excision of the primary tumour.
眼眶孤立性纤维瘤(SFT)是一种非常罕见的病变,可能被误诊为纤维组织细胞瘤、血管外皮细胞瘤或其他眼眶肿瘤。我们研究了一名35岁女性眼眶SFT的病例。
该患者有1年病史,自述右眼后方有“压迫”感,但无疼痛、视力变化或其他相关症状。眼部检查正常。磁共振成像(MRI)显示右眼眶内有一个边界清晰的内侧肿块。肿瘤被切除。
肿瘤为细胞性梭形细胞瘤,呈束状排列。肿瘤细胞呈梭形,核淡染,少见核分裂象。免疫组化显示波形蛋白和CD34阳性,但细胞角蛋白(AE1-AE3)、上皮膜抗原(EMA)、结蛋白、平滑肌肌动蛋白、S-100、CD31、CD45和bcl-2均为阴性。
SFT很少累及眼眶。必须完整切除肿瘤以避免复发。仔细并持续的随访很重要,因为眼眶复发可能在原发肿瘤切除数年之后发生。