Imashuku Shinsaku, Okazaki Nagisa ' Amamoto ', Nakayama Masahiko, Fujita Naoto, Fukuyama Tetsuhiro, Koike Kenichi, Minato Toshinori, Kobayashi Ryoji, Morimoto Akira
Division of Pediatrics, Takasago-seibu Hospital, Takasago, Japan.
Pediatr Blood Cancer. 2008 Feb;50(2):308-11. doi: 10.1002/pbc.21259.
In rare cases, patients with Langerhans cell histiocytosis (LCH) develop neurodegenerative CNS disease (ND-CNS-LCH). Management of ND-CNS-LCH has not been established.
We treated five pediatric patients with a combination of intravenous immunoglobulin (IVIG) and chemotherapy (steroid +/- vinblastine +/- 6-mercaptopurine +/- methotrexate). Prior to the therapy, three of the five patients had cerebellar ataxia while the remaining two had abnormal MRI findings without apparent neurological deficits. IVIG was given monthly or twice monthly at the dosage of 250-400 mg/kg/dose.
The four patients administered more than 23 doses of IVIG and chemotherapy remained in a stable condition and did not show significant progression signs in neurological deficits or brain MRI findings during the 30-month follow-up period (median; range: 19+ to 38+) following the initiation of therapy for ND-CNS-LCH.
The IVIG-containing treatment may be promising for ND-CNS-LCH; however, its effectiveness remains to be further tested in more patients as well as in a randomized trial.
在罕见情况下,朗格汉斯细胞组织细胞增多症(LCH)患者会发展为神经退行性中枢神经系统疾病(ND-CNS-LCH)。ND-CNS-LCH的治疗方法尚未确立。
我们用静脉注射免疫球蛋白(IVIG)和化疗(类固醇+/-长春花碱+/-6-巯基嘌呤+/-甲氨蝶呤)联合治疗了5名儿科患者。治疗前,5名患者中有3名患有小脑共济失调,其余2名患者MRI检查结果异常,但无明显神经功能缺损。IVIG每月或每半月给药一次,剂量为250 - 400mg/kg/剂量。
在开始针对ND-CNS-LCH进行治疗后的30个月随访期(中位数;范围:19 +至38 +)内,接受超过23剂IVIG和化疗的4名患者病情保持稳定,神经功能缺损或脑部MRI检查结果未显示出明显进展迹象。
含IVIG的治疗方法可能对ND-CNS-LCH有前景;然而,其有效性仍有待在更多患者中以及在随机试验中进一步检验。