Choi Sung W, Bangaru Babu S, Wu C Daniel, Finlay Jonathan L
Department of Pediatrics, New York University Medical Center, New York, New York, USA
J Pediatr Hematol Oncol. 2003 Jun;25(6):503-6. doi: 10.1097/00043426-200306000-00016.
Successful treatment of infants with gastrointestinal involvement in Langerhans cell histiocytosis (LCH) has been poor, with no specific chemotherapeutic regimen of clear benefit. An 8-month-old male, diagnosed with LCH by skin and gastrointestinal biopsies, was treated with several cycles of 2-chlorodeoxyadenosine, vinblastine and prednisone with only partial response. Ultimately, two cycles of 2-chlorodeoxyadenosine concomitant with high-dose cytarabine led to a durable complete response. Twenty-seven months since the last course of chemotherapy, the patient continues to thrive free of disease. Treatment with 2-chlorodeoxyadenosine and cytarabine should be considered for further study in patients with poor-prognosis LCH.
朗格汉斯细胞组织细胞增多症(LCH)累及胃肠道的婴儿的成功治疗情况一直不佳,尚无明确有益的特定化疗方案。一名8个月大的男性通过皮肤和胃肠道活检被诊断为LCH,接受了几个周期的2-氯脱氧腺苷、长春花碱和泼尼松治疗,仅部分缓解。最终,两个周期的2-氯脱氧腺苷联合大剂量阿糖胞苷导致了持久的完全缓解。自最后一个化疗疗程以来的27个月里,该患者持续健康成长,无疾病迹象。对于预后不良的LCH患者,应考虑使用2-氯脱氧腺苷和阿糖胞苷进行进一步研究。