MULTISYSTEM LANGERHANS CELL HISTIOCYTOSIS: CASE REPORT AND REVIEW OF THE LITERATURE
Journal Title: World Journal of Pharmaceutical Research - Year 2017, Vol 6, Issue 10
Abstract
Langerhans cell histiocytosis (LCH) is a rare and heterogeneous disease of unknown etiopathogenesis caused by clonal proliferation of Langerhans cells. We report a case of an adult woman diagnosed with Langerhans cell histiocytosis with neurological, endocrine and bone involvement. Clinicians should consider Langerhans cell histiocytosis in combination of central diabetes insipidus and lytic bone lesions.
Authors and Affiliations
J. Fatihi
Keywords
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