Bains Sukhdeep, Kim Usha, Shanti R
Department of Orbit, Oculoplasty and Ocular Oncology, Aravind Eye Hospitals and Postgraduate Institute of Ophthalmology, Madurai, Tamil Nadu, India.
Department of Pathology, Aravind Eye Hospitals and Postgraduate Institute of Ophthalmology, Madurai, Tamil Nadu, India.
Indian J Ophthalmol. 2016 Dec;64(12):932-934. doi: 10.4103/0301-4738.198849.
Primary orbital melanoma is rare and has varied initial presentation. A 28-year-old female presented with proptosis and decreased vision in the left eye. Computed tomography scan showed an orbital mass with contrast enhancement and calcification around the optic nerve leading to a diagnosis of meningioma. The patient chose to be on observation. Loss of vision with an increase in proptosis was seen at 6 months follow-up. On surgical exploration, a well-defined pigmented mass was seen encasing the optic nerve. Histopathological analysis revealed a malignant melanoma. Metastatic workup was negative. Left eye lid sparing exenteration was done. A high index of suspicion is necessary in a rapidly growing suspected optic nerve sheath meningioma and a differential diagnosis including orbital melanoma be considered.
原发性眼眶黑色素瘤罕见,其初始表现多样。一名28岁女性因左眼突出和视力下降就诊。计算机断层扫描显示眼眶有一肿块,有对比增强且视神经周围有钙化,诊断为脑膜瘤。患者选择观察。随访6个月时出现视力丧失且眼球突出加重。手术探查时,可见一个边界清晰的色素性肿块包绕视神经。组织病理学分析显示为恶性黑色素瘤。转移灶检查为阴性。进行了保留左眼眼睑的眼眶内容剜除术。对于快速生长的疑似视神经鞘脑膜瘤,必须保持高度怀疑,并考虑包括眼眶黑色素瘤在内的鉴别诊断。