Abstract
Histiocytic disorders in children and adults are caused by an abnormal accumulation of cells of the mononuclear phagocytic system. Langerhans cell histiocytosis (LCH) is a myeloid-derived dendritic cell disorder. The disease may affect any organ or system of the body, but those more frequently affected are the skin, bone and lymph nodes. Objectives: To evaluate characteristics of demography, location of lesions and histopathology of LCH. Methods: Cross sectional study of 80 children who have been performed biopsy with pathological diagnosis of LCH at Children’s Hospital 1 from Jan 2015 to Dec 2019. Results: LCH was encountered in children from 1 month to 12 years old in the study population. The mean age is 3.1 ± 2.7 (years) and in both male and female (M: F= 1.7/1). The most frequent sites of lession are skin and soft tissues. Conclusion: Langerhans cell histiocytosis is a malignant disease that may be encountered in clinical practice with different sites of lesions. LCH should be thought of when suspected and diagnosed early by histopathology to help guide treatment promptly and appropriately
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