Liver Involvement in Langerhans’ Cell Histiocytosis. Case Report
Keywords:
Langerhans'cell histiocytosis, diabetes insipidus, S100 proteinAbstract
Langerhans'cell histiocytosis (Histiocytosis X) is a rare disease of unknown cause characterized by oligoclonal proliferation of Langerhans cells. It occurs mostly in children and young adults and involves one or more body systems such as bone, hypothalamus, posterior pituitary gland, lymph nodes, liver or various soft tissues.The diagnosis is always made by a histological approach.We report a case of Langerhans'cell histiocytosis in a young patient with clinical signs of diabetes insipidus and hepatic involvement in whom the immunohistochemical analysis of the liver tissue led to the definitive diagnosis.
Downloads
Published
2006-03-01
How to Cite
1.
Dina I, Copaescu C, Herlea V, Wrba F, Iacobescu C. Liver Involvement in Langerhans’ Cell Histiocytosis. Case Report. JGLD [Internet]. 2006 Mar. 1 [cited 2026 Jul. 17];15(1):57-9. Available from: https://www.jgld.ro/jgld/index.php/jgld/article/view/2006.1.9
Issue
Section
Case Reports

