ea0063p269 | Pituitary and Neuroendocrinology 1 | ECE2019
Barcelo Carlos Antich
, Soler Guillermo Serra
, Font Mercedes Noval
, Ribas Elena Mena
, Povidano Santiago Tofe
, Jimenez Inaki Arguelles
, Fernandez Honorato Garcia
, Macazaga Vicente Pereg
Introduction: Langerhans cell histiocytosis (LCH) is a rare systemic disease. Diabetes insipidus is the most frequent endocrine alteration and occurs mostly after diagnosis. Others are hypogonadism, growth hormone deficiency (GHD) and alterations in glucose metabolism.Clinical case: A 61-year-old smoker, diagnosed with LCH 9 years ago with pulmonary and hepatic involvement, without treatment, who consulted for asthenia, unquantifiable polyuria, polydipsi...