Okujima Nami, Iimori Hirohito, Shiraishi Atsushi
Department of Ophthalmology, Ehime University School of Medicine, Toon, JPN.
Cureus. 2025 Jan 7;17(1):e77094. doi: 10.7759/cureus.77094. eCollection 2025 Jan.
Ophthalmic manifestations are a common occurrence in leukaemia cases and may result from a number of factors, including direct leukemic infiltration, haematologic abnormalities, central nervous system (CNS) involvement, or treatment-related effects. This case report discusses a paediatric patient with acute lymphoblastic leukaemia (ALL) who developed recurrent ocular symptoms, including retinitis pigmentosa-like findings, which is degeneration with pigment neopigmentation in the mid- to peripheral fundus, during remission, underscoring the necessity of continuous monitoring. A four-year-old female with a history of ALL, diagnosed at two years and three months of age, presented with ophthalmic complications during remission. The leukaemia was characterised by positivity for CD20, CD19, and the mature B-cell antigen, as well as a KMT2A-AFF1 gene rearrangement. Despite the administration of an intensive chemotherapy regimen and CAR-T cell therapy, the patient experienced a relapse and subsequently underwent umbilical cord blood transplantation, resulting in the attainment of molecular remission. However, at three years and seven months of age, a notable increase in the size of the left orbital tumour was observed. At three years and 11 months of age, the patient exhibited retinal changes that were consistent with retinitis pigmentosa, as confirmed by fundus photography. Additional findings included moderate left pupil dilation, an absent light reflex, optic disc swelling, dilated retinal vessels, and a serous retinal detachment. The presence of KMT2A-AFF1 mRNA in the anterior chamber fluid served to confirm the occurrence of an ocular relapse, a finding that was also evident in the bone marrow analysis. The patient was treated with salvage chemotherapy and localised radiation therapy (24 Gy) to the left eye, resulting in partial resolution of symptoms. At the four-year and three-month follow-up, retinitis pigmentosa-like changes with proliferative alterations persisted, although the serous retinal detachment had resolved. This case demonstrates that ophthalmic manifestations can occur even during the remission phase of leukaemia, emphasising the importance of regular, multidisciplinary follow-up.
眼部表现是白血病病例中的常见现象,可能由多种因素引起,包括白血病细胞直接浸润、血液学异常、中枢神经系统(CNS)受累或治疗相关影响。本病例报告讨论了一名患有急性淋巴细胞白血病(ALL)的儿科患者,该患者在缓解期出现复发性眼部症状,包括色素性视网膜炎样表现,即眼底中周部出现色素沉着的退行性变,强调了持续监测的必要性。一名4岁女性,有ALL病史,于2岁3个月时确诊,在缓解期出现眼部并发症。该白血病的特征是CD20、CD19和成熟B细胞抗原呈阳性,以及KMT2A - AFF1基因重排。尽管给予了强化化疗方案和嵌合抗原受体T细胞(CAR - T)疗法,但患者仍复发,随后接受了脐带血移植,实现了分子缓解。然而,在3岁7个月时,观察到左眼眶肿瘤大小显著增加。在3岁11个月时,经眼底照相证实患者出现了与色素性视网膜炎一致的视网膜变化。其他发现包括左瞳孔中度散大、光反射消失、视盘肿胀、视网膜血管扩张和浆液性视网膜脱离。前房液中存在KMT2A - AFF1 mRNA证实了眼部复发的发生,这一发现在骨髓分析中也很明显。患者接受了挽救性化疗和左眼局部放射治疗(24 Gy),症状部分缓解。在4岁3个月的随访中,尽管浆液性视网膜脱离已消退,但色素性视网膜炎样改变及增殖性改变仍然存在。本病例表明,即使在白血病缓解期也可能出现眼部表现,强调了定期进行多学科随访的重要性。