ESPE Abstracts

Introduction: Langerhans cell histiocytosis (LCH) is a rare disease that the clinical presentation can vary from the involvement of a single region to widespread multiorgan involvement. The most common central nervous system infiltration is observed in the hypothalamic-pituitary region, which frequently leads to central diabetes insipidus (CDİ) and occasionally to anterior pituitary hormone deficiencies. There is limited data on endocrinological findings,...