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白血病中枢神经系统治疗引起的神经毒性。

Neurotoxicity due to CNS therapy for leukemia.

作者信息

Pochedly C

出版信息

Med Pediatr Oncol. 1977;3(1):101-15. doi: 10.1002/mpo.2950030114.

DOI:10.1002/mpo.2950030114
PMID:840159
Abstract

CNS symptoms ranging from mild to lethal have occurred following CNS radiotherapy and intrathecal chemotherapy. Cranial radiotherapy often produces signs of mild encephalopathy, with predominance of somnolence. In rare cases, it appears that CNS radiotherapy may be followed by progressive encephalopathy. Intrathecal methotrexate frequently causes symptoms of meningeal irritation. Occasionally cases of weakness and paralysis, and rare instances of severe encephalopathy, may occur. However, in leukemic children treated with intensive chemotherapy and CNS radiotherapy who develop neurological complications, it is often difficult to determine which of many possible factors may be causing the CNS symptoms. The pathogenesis of the various forms of methotrexate neurotoxicity is poorly understood. The best-established cause for these symptoms is high concentrations of methotrexate in the CSF or porlonged exposure of the brain to low CSF concentrations of methotrexate. These elevated concentrations of the drug may in turn be due to impaired elimination of the drug from the cerebrospinal fluid (usually due to overt CNS leukemia) or to increased dosage in relation to cerebrospinal fluid volume (due to adolescent age). Leukoencephalopathy is occasionally found at autopsy in children given intensive therapy with CNS radiotherapy and intrathecal methotrexate, together with intensive systemic chemotherapy. It was proposed that alteration of the blood-brain barrier by cranial radiotherapy allows systemically administered anti-leukemic drugs to enter the brain and to cause necrotic changes in the CNS white matter. Leukoencephalopathy also occurs following intraventricular administration of methotrexate. CNS-toxicity due to intrathecal cytosine arabinoside is clinically similar to the symptoms seen following intrathecal methotrexate.

摘要

中枢神经系统放疗和鞘内化疗后曾出现过从轻度到致命的中枢神经系统症状。颅脑放疗常产生轻度脑病的体征,以嗜睡为主。在罕见情况下,中枢神经系统放疗后似乎可能会出现进行性脑病。鞘内注射甲氨蝶呤常引起脑膜刺激症状。偶尔会出现虚弱和瘫痪病例,以及罕见的严重脑病病例。然而,在接受强化化疗和中枢神经系统放疗并出现神经并发症的白血病儿童中,往往很难确定众多可能因素中哪一个可能导致中枢神经系统症状。各种形式的甲氨蝶呤神经毒性的发病机制尚不清楚。这些症状最确定的原因是脑脊液中甲氨蝶呤浓度高或大脑长期暴露于脑脊液中甲氨蝶呤的低浓度。这些药物浓度升高反过来可能是由于药物从脑脊液中的清除受损(通常由于明显的中枢神经系统白血病)或相对于脑脊液量的剂量增加(由于青春期)。在接受中枢神经系统放疗、鞘内注射甲氨蝶呤以及强化全身化疗的强化治疗的儿童尸检中偶尔发现白质脑病。有人提出,颅脑放疗引起的血脑屏障改变使全身给药的抗白血病药物进入大脑并导致中枢神经系统白质发生坏死性变化。脑室内注射甲氨蝶呤后也会发生白质脑病。鞘内注射阿糖胞苷引起的中枢神经系统毒性在临床上与鞘内注射甲氨蝶呤后出现的症状相似。

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Neurotoxicity due to CNS therapy for leukemia.白血病中枢神经系统治疗引起的神经毒性。
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Acute encephalopathy after initiation of cranial irradiation for meningeal leukaemia.脑膜白血病进行颅脑照射后发生的急性脑病。
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