Searchable abstracts of presentations at key conferences in endocrinology

ea0049ep837 | Clinical case reports - Pituitary/Adrenal | ECE2017

Multifocal multisystem langerhans cell histiocytosis – a rare cause of panhypopituitarism and diabetes insipidus – a case report

Gabalec Filip , Simkovic Martin , Kasparova Petra , Zak Pavel , Cap Jan

Introduction: Langerhans cell histiocytosis (LCH) is a very rare disease in adults and as well a very rare cause of sellar expansion. The clinical presentation can be heterogeneous, from a single bone lesion to potentially fatal, widespread disease. We describe the difficulties with the evaluation and the treatment of LCH.Case: 39 years old woman has had amenorrhea for 2 years and higher intake of fluids (5–7 l/day) for 6 years. Non-functioning pitu...