A rare cause of hepatosplenomegaly: Langerhans cell histiocytosis

References (1)

1. Langerhans cell histiocytosis (LHH) is a rare disease with infiltration and monoclonal proliferation, typically infant and organs with mononuclear phagocytic systems therein. The most common bone involvement (osteolytic lesions) and the second most common skin involvement. Since Langerhans cell histiocyte cells are present in many places in our body, they can also produce symptoms with rare symptoms. In this case, a 9-month-old girl with fever, hepatosplenomegaly, papular, seborrheic dermatitis on hands and diagnosed as LHH was examined.