中华医学杂志（英文版）2012，Vol.125Issue(9)：1675-1676,2.DOI:10.3760/cma.j.issn.0366-6999.2012.09.031
A child with pulmonary and liver Langerhans'-cell histiocytosis
A child with pulmonary and liver Langerhans'-cell histiocytosis
MA Xiao-li 1SHEN Kun-ling 1WANG Bin1
作者信息
- 1. Hematology Center, Beijing Children's Hospital Affiliated to Capital Medical University, Beijing 100045, China
- 折叠
摘要
Abstract
Clinical categories of Langerhans cell histiocytosis (LCH) include single and multi-system disease.Pulmonary LCH is rare,which is an unusual interstitial lung disease with the characteristics of monoclonal proliferation and infiltration of Langerhans' cells to organs.We report our experience of a rare LCH case of multiple organs such as pulmonary and liver as the main clinical manifestation.The patient was treated with chemotherapy which included prednisone,vinblastine,methotrexate and 6-mercaptopurine for 52 weeks and follow up all along.The patient has a favorable clinical outcome.关键词
Langerhans '-cell histiocytosis/pulmonary/liver, childKey words
Langerhans '-cell histiocytosis/pulmonary/liver, child引用本文复制引用
MA Xiao-li,SHEN Kun-ling,WANG Bin..A child with pulmonary and liver Langerhans'-cell histiocytosis[J].中华医学杂志（英文版）,2012,125(9):1675-1676,2.
