Langerhans cell histiocytosis and neuroblastoma: report of two cases with follow-up for over 3 years

被引:0
作者
Huang, Cheng [1 ,2 ,3 ,4 ]
Zhang, Li [1 ,2 ,3 ,4 ]
Jin, Mei [1 ,2 ,3 ,4 ]
Ge, Xinshun [3 ,4 ]
Qin, Hong [3 ,4 ]
Zhou, Chunju [3 ,4 ]
Zhang, Rui [1 ,2 ,3 ,4 ]
Ma, Xiaoli [1 ,2 ,3 ,4 ]
机构
[1] Capital Med Univ, Minist Educ, Beijing Key Lab Pediat Hematol Oncol, 56 Nanlishi Rd, Beijing 100045, Peoples R China
[2] Capital Med Univ, Minist Educ, Natl Key Discipline Pediat, 56 Nanlishi Rd, Beijing 100045, Peoples R China
[3] Capital Med Univ, Hematol Oncol Ctr, 56 Nanlishi Rd, Beijing 100045, Peoples R China
[4] Capital Med Univ, Beijing Childrens Hosp, 56 Nanlishi Rd, Beijing 100045, Peoples R China
关键词
Langerhans cell histiocytosis; neuroblastoma; follow up;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Langerhans cell histiocytosis (LCH) is a clinically heterogeneous disorder characterized by proliferation of abnormal bone marrow derived dendritic cells. Neuroblastoma (NB) is embryonal tumors that form around sympathetic nerve ganglions. It is the most extracranial malignant tumor type. We present 2 patients who developed LCH and NB. Up to July 31, 2015, these 2 patients have been followed up over 3 years, the prognosis are optimistic. Here we introduce our experiences during the therapeutic process of the 2 cases.
引用
收藏
页码:2702 / 2705
页数:4
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