一例Crigler-Najjar综合征患者原发性中枢神经系统淋巴瘤的病例报告及文献复习:我们如何处理

IF 0.3 Q4 ONCOLOGY
Udip Maheshwari, Disha Morzaria, Seema Jagiasi, Vashishth Maniar, Ashish Joshi, Sameer Soneji
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引用次数: 0

摘要

原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见的中枢神经系统肿瘤,可以使用大剂量化疗药物进行治疗。大剂量甲氨蝶呤是治疗PCNSL的必备药物。我们报告了一例26岁的男性,已知患有Crigler-Najjar综合征II型合并症,基线胆红素为13.5 mg/dL,表现为嗜睡和共济失调。鉴于高胆红素血症,针对该患者修改了CNS淋巴瘤的最佳治疗方案,即De Angelis方案。患者对化疗耐受良好,胆红素水平波动可控,随后进行全脑放疗。他在出现症状6个月后仍无症状,病情完全缓解。我们在这里强调这个不寻常的PCNSL的情况下,高剂量甲氨蝶呤使用密切观察肝功能鉴于高胆红素血症在一个已知的病例克里格勒-纳贾尔综合征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case Report and Literature Review of Primary Central Nervous System Lymphoma in a Patient with Crigler–Najjar Syndrome: How We Managed
Abstract Primary central nervous system lymphoma (PCNSL) is a rare form of CNS tumor that can be managed with curative intent using high-dose chemotherapeutic drugs. High-dose methotrexate is an essential drug for the management of PCNSL. We present a case of a 26-year-old man with a known comorbidity of Crigler–Najjar syndrome type II and a baseline bilirubin of 13.5 mg/dL, presented with somnolence and ataxia. In view of hyperbilirubinemia, the optimal treatment for CNS lymphoma, the De Angelis protocol, was modified for this patient. The patient tolerated the chemotherapy well with manageable fluctuations in bilirubin levels, followed by consolidation with whole-brain radiotherapy. He remains asymptomatic 6 months after the onset of the symptoms with the disease in complete remission. We highlight here this unusual case of PCNSL where high-dose methotrexate was used with close observation of liver function in view of hyperbilirubinemia in a known case of Crigler–Najjar syndrome.
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来源期刊
CiteScore
0.40
自引率
0.00%
发文量
91
期刊介绍: The journal will cover technical and clinical studies related to medical and pediatric oncology in human well being including ethical and social issues. Articles with clinical interest and implications will be given preference.
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