Okada Arisa, Harada Yosuke, Inoue Tomoko, Okikawa Yoshiko, Ichinohe Tatsuo, Kiuchi Yoshiaki
Department of Ophthalmology and Visual Science, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Department of Hematology and Oncology, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Am J Ophthalmol Case Rep. 2018 May 17;11:37-40. doi: 10.1016/j.ajoc.2018.05.002. eCollection 2018 Sep.
To report a rare case of primary orbital natural killer (NK)/T-cell lymphoma without nasal lesions but with cerebrospinal fluid involvement.
A 73-year-old woman was referred to the uveitis clinic with suspected unilateral acute uveitis in her right eye and a right orbital tumor. Epstein-Barr virus DNA was detected in the aqueous humor in her right eye, and orbital biopsy revealed the presence of extranodal NK/T-cell lymphoma (ENKTL), nasal type. Positron emission tomography showed significant F-fluorodeoxyglucose uptake in the right orbit, with no other signs of systemic involvement. Cerebrospinal fluid analysis demonstrated lymphoma cell infiltration. She was diagnosed with stage IV ENKTL and treated with orbital radiotherapy and systemic chemotherapy, with subsequent remission. However, the lymphoma relapsed in her left vitreous at 10 months after therapy, suggesting metastasis of lymphoma cells to the contralateral eye via the vitreous and cerebrospinal fluid.
A few cases of ocular-tissue ENKTL have been reported, mostly involving invasion or dissemination of primary nasal lesions; in contrast, primary orbital and intraocular ENKTL has rarely been reported. To the best of our knowledge, this is the first report of a primary orbital ENKTL metastasizing to the vitreous of the contralateral eye. Although ENKTL is rare in the orbit and intraocular tissues, it should be considered as a possible differential diagnosis in patients with orbital tumors or intraocular inflammation resistant to steroid therapy because ENKTL has a very poor prognosis in the advanced stage.
报告一例罕见的原发性眼眶自然杀伤(NK)/T细胞淋巴瘤,无鼻部病变但有脑脊液受累。
一名73岁女性因右眼疑似单侧急性葡萄膜炎和右眼眶肿瘤被转诊至葡萄膜炎诊所。右眼房水中检测到爱泼斯坦-巴尔病毒DNA,眼眶活检显示存在鼻型结外NK/T细胞淋巴瘤(ENKTL)。正电子发射断层扫描显示右眼眶有明显的F-氟脱氧葡萄糖摄取,无其他全身受累迹象。脑脊液分析显示有淋巴瘤细胞浸润。她被诊断为IV期ENKTL,并接受了眼眶放疗和全身化疗,随后病情缓解。然而,治疗10个月后淋巴瘤在她的左眼玻璃体复发,提示淋巴瘤细胞通过玻璃体和脑脊液转移至对侧眼。
已有少数眼组织ENKTL病例报道,大多涉及原发性鼻部病变的侵袭或播散;相比之下,原发性眼眶和眼内ENKTL鲜有报道。据我们所知,这是首例原发性眼眶ENKTL转移至对侧眼玻璃体的报告。尽管ENKTL在眼眶和眼内组织中罕见,但对于对类固醇治疗耐药的眼眶肿瘤或眼内炎症患者,应将其视为可能的鉴别诊断,因为晚期ENKTL预后极差。