Nakamura Takuji, Nishi Masanori, Rikitake Mihoko, Koga Daisuke, Eto Junya, Tajima Daisuke, Toda Shuji, Matsuo Muneaki
Department of Pediatrics, Faculty of Medicine, Saga University, 5-1-1 Nabeshima, Saga 849-8501, Japan; Department of Pediatrics, National Hospital Organization Ureshino Medical Center, 2436 Ureshino, Saga 843-0393, Japan.
Department of Pediatrics, Faculty of Medicine, Saga University, 5-1-1 Nabeshima, Saga 849-8501, Japan.
Brain Dev. 2019 Jan;41(1):111-115. doi: 10.1016/j.braindev.2018.07.006. Epub 2018 Aug 10.
Subacute combined degeneration of the spinal cord (SACD) is a rare neurologic disorder manifesting progressive symptoms of paresthesia and spastic paralysis. Herein we present an autopsy case of SACD caused by folic acid and copper deficiency. A 16-year-old male presented with gradually worsening unsteady gait, and bladder and rectal dysfunction. He had a medical history of T-cell acute lymphoblastic leukemia (T-ALL), diagnosed 1.5 years previously. The patient had undergone chemotherapy, including methotrexate, as well as allogeneic bone mallow transplantation. Laboratory tests revealed normal vitamin B and methylmalonic acid concentration, but reduced serum copper, ceruloplasmin and folic acid concentrations. Magnetic resonance imaging revealed symmetrical T2 signal hyperintensities in the posterior and lateral spinal cord. The patient was treated with oral copper, oral folate, and intravenous vitamin B. A month after this treatment, the patient's symptoms were unchanged, and 2 months later he died of acute adrenal insufficiency. The pathological findings of the spinal cord were compatible with SACD. Because SACD is usually reversible with early treatment, it should be suspected in high-risk patients undergoing chemotherapy or those who are malnourished with characteristic symptoms of SACD, even in young patients.
脊髓亚急性联合变性(SACD)是一种罕见的神经系统疾病,表现为进行性感觉异常和痉挛性瘫痪症状。在此,我们报告一例由叶酸和铜缺乏引起的SACD尸检病例。一名16岁男性患者出现步态逐渐不稳以及膀胱和直肠功能障碍。他有1.5年前诊断为T细胞急性淋巴细胞白血病(T-ALL)的病史。该患者接受了包括甲氨蝶呤在内的化疗以及异基因骨髓移植。实验室检查显示维生素B和甲基丙二酸浓度正常,但血清铜、铜蓝蛋白和叶酸浓度降低。磁共振成像显示脊髓后部和外侧对称的T2信号高增强。患者接受了口服铜、口服叶酸和静脉注射维生素B治疗。治疗一个月后,患者症状未改善,两个月后死于急性肾上腺功能不全。脊髓的病理 findings与SACD相符。由于SACD通常早期治疗可逆转,对于接受化疗的高危患者或有SACD特征性症状的营养不良患者,即使是年轻患者,也应怀疑该病。 (原文中“findings”拼写错误,正确拼写为“findings” )