CENTRAL DIABETES INSIPIDUS REVEALING A MULTISYSTEM LANGERHANS CELL HISTIOCYTOSIS : A CASE REPORT
Zineb Serhane
, Meryem El Adla
, Zineb EL Azime
, Mohammed-Amine Essafi
, Hayat Aynaou
and Houda Salhi
- 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
- Keywords
- Cite This Article as
- Corresponding Author
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.
[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 Int. J. of Adv. Res. (Nov). 169-177] (ISSN 2320-5407). www.journalijar.com
Department of Endocrinology, Diabetology, Metabolic Diseases and Nutrition, Hassan II University Hospital, Fes, Morocco.
Morocco
