| Literature DB >> 11402519 |
I Ben Ghorbel1, M H Houman, S B'chir, S Chamakhi, M Miled.
Abstract
INTRODUCTION: Langerhans' cell histiocytosis is a rare disorder of unknown etiology characterized by a wide clinical spectrum and varied behavior. Diabetes insipidus is a relatively common feature in Langerhans' cell histiocytosis. The presence of both diabetes insipidus and mellitus associated with histiocytosis in an adult is rare. To our knowledge, only three previous cases have been reported. EXEGESIS: We report the clinical presentation, pathologic findings and clinical progress in an adult female who had disseminated Langerhans' cell histiocytosis (hypothalamic infiltration, multifocal bone involvement) associated with both diabetes insipidus and mellitus.Entities:
Mesh:
Year: 2001 PMID: 11402519 DOI: 10.1016/s0248-8663(01)00373-3
Source DB: PubMed Journal: Rev Med Interne ISSN: 0248-8663 Impact factor: 0.728