Isolated Optic Nerve Relapse in a Pediatric Patient With T-Cell Lymphoblastic Leukemia: A Brief Report.

IF 0.9 4区 医学 Q4 HEMATOLOGY Journal of Pediatric Hematology/Oncology Pub Date : 2024-08-01 Epub Date: 2024-06-04 DOI:10.1097/MPH.0000000000002893
Rakefet Shenkar, Samir B Kahwash, Diana P Rodriguez, Rolla Abu Arja, Suzanne M Reed, Hemalatha G Rangarajan
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Abstract

Isolated optic nerve (ON) relapse is a rare occurrence in lymphoblastic leukemia (LBL). A 10-year-old boy with T-LBL presented 8 months after diagnosis with blurred vision and thickening of right ON on magnetic resonance imaging consistent with relapse. Cerebrospinal fluid and bone marrow were negative for leukemia. He received reinduction chemotherapy (including nelarabine and craniospinal radiation) followed by a myeloablative matched sibling donor bone marrow transplant. He remains in remission 2 years post-transplant with normal vision. We also review the literature for reports of isolated ON relapse in patients with LBL. Our patient's clinical course demonstrates that disease control can be achieved with early detection of ON relapse before disease progression.

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一名 T 细胞淋巴细胞白血病儿科患者的孤立性视神经复发:简要报告。
淋巴细胞白血病(LBL)中罕见孤立性视神经(ON)复发。一名患有T-LBL的10岁男孩在确诊8个月后出现视力模糊,磁共振成像显示右侧视神经增粗,与复发一致。脑脊液和骨髓检查均为阴性。他接受了恢复性化疗(包括奈拉滨和颅骨放射治疗),随后接受了骨髓移植。移植后两年,他的病情仍在缓解,视力正常。我们还查阅了有关LBL患者孤立性ON复发的文献报道。我们患者的临床病程表明,如果能在疾病进展之前及早发现ON复发,就能控制疾病。
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来源期刊
CiteScore
1.90
自引率
8.30%
发文量
415
审稿时长
2.5 months
期刊介绍: ​Journal of Pediatric Hematology/Oncology (JPHO) reports on major advances in the diagnosis and treatment of cancer and blood diseases in children. The journal publishes original research, commentaries, historical insights, and clinical and laboratory observations.
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