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WJPR Citation
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| All | Since 2020 | |
| Citation | 8502 | 4519 |
| h-index | 30 | 23 |
| i10-index | 227 | 96 |
MULTISYSTEM LANGERHANS CELL HISTIOCYTOSIS: CASE REPORT AND REVIEW OF THE LITERATURE
J. Fatihi*, S. Bellasri, H. Janah, R. Akka, T. Aatif and A. C. El Asri
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. Keywords: Langerhans Cell Histiocytosis, Bone, Central nervous system. [Full Text Article] [Download Certificate] |
