Liver Involvement in Langerhans’ Cell Histiocytosis. Case Report

Authors

  • Ion Dina Medical Clinic," Sf.Ioan" Hospital, Bucharest, Romania
  • Catalin Copaescu Surgical Clinic," Sf.Ioan" Hospital, Bucharest, Romania
  • Vlad Herlea Department of Pathology, Fundeni Clinical Institute, Bucharest, Romania
  • Fritz Wrba Department of Clinical Pathology, University of Vienna - Medical School, Austria
  • Claudia Iacobescu Medical Clinic," Sf.Ioan" Hospital, Bucharest, Romania

Keywords:

Langerhans'cell histiocytosis, diabetes insipidus, S100 protein

Abstract

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.

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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

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Section

Case Reports