Endocrine Abstracts

Introduction: Langerhans cell histiocytosis (LCH) is a very rare haematological disease, with difficult diagnosis for its very variable clinical picture. It is caused by monoclonal proliferation of cutaneous Langerhans cells. It affects most commonly the skin and bones, less often bone marrow, liver, pituitary and CNS.Case report: A 74-year-old female patient with progressive sclerosing cholangitis was referred to a transplant centre to consider liver tr...