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
- How to Cite This Article
- 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., 13 (11), 169-177, ISSN 2320-5407. DOI URL: https://dx.doi.org/10.21474/IJAR01/22101
Department of Endocrinology, Diabetology, Metabolic Diseases and Nutrition, Hassan II University Hospital, Fes, Morocco.
Morocco
