Matsuo Toshihiko, Yano Tomofumi, Yoshio Kotaro, Tanaka Takehiro, Nishimura Hirotake, Matsuoka Ken-Ichi
Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University, Okayama, JPN.
Department of Ophthalmology, Okayama University Hospital, Okayama, JPN.
Cureus. 2025 Jun 10;17(6):e85680. doi: 10.7759/cureus.85680. eCollection 2025 Jun.
Involved-site radiation therapy is effective for curative and palliative treatments of cancers, including lymphoma. This case study describes the use of whole-eye radiation for primary intraocular lymphoma occurring during primary central nervous system lymphoma. The patient, a 68-year-old man, developed personality changes and apathy two weeks after cataract surgery combined with vitrectomy for vitreous opacity in the left eye. Magnetic resonance imaging revealed a mass lesion in the left frontal lobe, and biopsy by craniotomy confirmed diffuse large B-cell lymphoma. He underwent chemotherapy using rituximab combined with high-dose methotrexate and high-dose cytarabine in association with intrathecal methotrexate and cytarabine injections, leading to complete remission. At age 75, he noticed forgetfulness, and fluorodeoxyglucose positron emission tomography and magnetic resonance imaging revealed a relapse of lymphoma in the splenium of the corpus callosum. He underwent chemotherapy using rituximab combined with high-dose methotrexate, followed by monthly rituximab monotherapy for one year and then rituximab monotherapy every two months for one year. He maintained complete remission with no treatment until age 78, when he developed subretinal choroidal lesions in the left eye and underwent whole-eye radiation at 40 Gy. One year later, he developed subretinal choroidal lesions in the right eye and underwent whole-eye radiation at 40 Gy. At age 81, he had lower limb weakness with disorientation. Magnetic resonance imaging showed a relapse of lymphoma in the right frontal to temporal lobe. The brain lesions showed a marked response to four weeks of oral tirabrutinib as a salvage therapy, but the lesions regrew, and the patient died seven months later. Throughout the treatment, he maintained a visual acuity of 0.7 (decimal scale) in both eyes. In conclusion, whole-eye radiation should be considered as a treatment option for the local control of active intraocular lymphoma, especially choroidal lesions, for patients with primary central nervous system lymphoma with no active brain lesions and without systemic treatment.
受累部位放射治疗对包括淋巴瘤在内的多种癌症的根治性和姑息性治疗均有效。本病例研究描述了在原发性中枢神经系统淋巴瘤期间发生的原发性眼内淋巴瘤采用全眼放射治疗的情况。患者为一名68岁男性,在因左眼玻璃体混浊行白内障手术联合玻璃体切除术后两周出现性格改变和淡漠。磁共振成像显示左额叶有一肿块病变,开颅活检证实为弥漫性大B细胞淋巴瘤。他接受了利妥昔单抗联合大剂量甲氨蝶呤和大剂量阿糖胞苷化疗,并鞘内注射甲氨蝶呤和阿糖胞苷,实现了完全缓解。75岁时,他出现记忆力减退,氟脱氧葡萄糖正电子发射断层扫描和磁共振成像显示胼胝体压部淋巴瘤复发。他接受了利妥昔单抗联合大剂量甲氨蝶呤化疗,随后每月接受利妥昔单抗单药治疗一年,然后每两个月接受利妥昔单抗单药治疗一年。在78岁之前未进行治疗的情况下他一直保持完全缓解,直到那时他左眼出现视网膜下脉络膜病变,并接受了40 Gy的全眼放射治疗。一年后,他右眼出现视网膜下脉络膜病变,并接受了40 Gy的全眼放射治疗。81岁时,他出现下肢无力和定向障碍。磁共振成像显示右额叶至颞叶淋巴瘤复发。脑部病变对作为挽救治疗的四周口服替拉布替尼有明显反应,但病变复发,患者七个月后死亡。在整个治疗过程中,他双眼视力均维持在0.7(十进制视力表)。总之,对于没有活动性脑病变且未进行全身治疗的原发性中枢神经系统淋巴瘤患者,全眼放射治疗应被视为局部控制活动性眼内淋巴瘤尤其是脉络膜病变的一种治疗选择。