Objective to explore the clinical and laboratory characteristics of langerhans cell histiocytosis (LCH) in children, so as to improve diagnosis level and decrease misdiagnosis rate.
目的探讨郎格罕组织细胞增生症(LCH)的临床特征，以提高诊断水平，减少误诊率。
Histiocytosis associated with disturbance of cholesterol metabolism, occurs chiefly in young children.
代谢障碍有关的组织细胞增多症，通常发生在年轻人身上。
Histiocytosis associated with disturbance of cholesterol metabolism, occurs chiefly in young children.
代谢障碍有关的组织细胞增多症，通常发生在年轻人身上。
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