Department of Ophthalmic Plastic Surgery and Ocular Oncology, PBMA's H V Desai Eye Hospital, Pune, Maharashtra, India.
Department of Histopathology, Ruby Hall Clinic, Pune, Maharashtra, India.
Ophthalmic Plast Reconstr Surg. 2019 Mar/Apr;35(2):e27-e29. doi: 10.1097/IOP.0000000000001293.
A 71-year-old male presented with a history of noticing gradual painless progressive proptosis along with a pinkish mass seen on the outer aspect of his left eyeball. Orbital CT revealed a fairly defined homogenous lesion, abutting the left eyeball and involving the lateral orbit reaching almost till orbital apex. Histopathology analysis aided with immunohistochemistry after an incision biopsy was consistent with leiomyosarcoma. Positron emission tomography scan ruled out presence of any distant primary or metastatic tumor. He underwent eyelid sparing total orbital exenteration with confirmed tumor free soft-tissue margins. He is doing well at 5 months of follow-up with no sign of local recurrence or distant metastasis. Primary orbital leiomyosarcoma is a rare tumor. It is mainly found in older woman; it is even rarer in males. Complete surgical excision with tumor free margins is the recommended treatment. Histopathology and immunohistochemistry are valuable in diagnosis and management.
一位 71 岁男性,自述左眼逐渐出现无痛性进行性突出,并在外眼部可见粉红色肿块。眼眶 CT 显示一个相当明确的均匀病变,紧贴左眼球并累及外侧眼眶,几乎到达眶尖。经切开活检后,组织病理学分析结合免疫组化检查结果与平滑肌肉瘤一致。正电子发射断层扫描排除了任何远处原发性或转移性肿瘤的存在。他接受了保留眼睑的全眼眶内容物切除术,证实软组织边缘无肿瘤。在 5 个月的随访中,他恢复良好,没有局部复发或远处转移的迹象。原发性眼眶平滑肌肉瘤是一种罕见的肿瘤。它主要发生在老年女性中,在男性中更为罕见。推荐的治疗方法是彻底切除肿瘤并保证边缘无肿瘤。组织病理学和免疫组化在诊断和治疗中具有重要价值。