CENTRAL DIABETES INSIPIDUS REVEALING A MULTISYSTEM LANGERHANS CELL HISTIOCYTOSIS : A CASE REPORT
- Department of Endocrinology, Diabetology, Metabolic Diseases and Nutrition. Hassan II University Hospital Center. Fez. Morocco.
- Laboratory of Epidemiology, Research in Health Sciences, Faculty of Medicine and Pharmacy, USMBA, Fez, Morocco.
Abstract
Introduction: Langerhans Cell Histiocytosis (LCH) is a rare myeloid precursor disorder primarily affecting young individuals, in which hypothalamic-pituitary involvement is uncommon but often diagnostically challenging due to non-specific clinical and radiological features.
Conclusion : This case highlights the diagnostic value of skin biopsy in inaccessible lesions and the importance of early diagnosis and multidisciplinary intervention in aggressive multisystemic LCH.
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Zineb Serhane, Meryem El Adla, Zineb EL Azime, Mohammed-Amine Essafi, Hayat Aynaou and Houda Salhi (2025); CENTRAL DIABETES INSIPIDUS REVEALING A MULTISYSTEM LANGERHANS CELL HISTIOCYTOSIS : A CASE REPORT, International Journal of Advanced Research (IJAR), 13 (11), 169-177, ISSN 2320-5407. DOI: https://doi.org/10.21474/IJAR01/22101
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