Publication details

Centrální diabetes insipidus - první příznak histiocytózy z Langerhansových buněk a Erdheimovy - Chesterovy choroby dospělých osob. Popis tří případů a přehled literatury

Title in English Central diabetes insipidus in adult patients--the first sign of Langerhans cell histiocytosis and Erdheim-Chester disease. Three case studies and literature review
Authors

ADAM Zdeněk BALŠÍKOVÁ Karola KREJČÍ Marta POUR Luděk ŠTĚPÁNKOVÁ Soňa SVAČINA Petr HERMANOVÁ Markéta VANÍČEK Jiří KRUPA Petr STANÍČEK Jiří KOUKALOVÁ Renata NEUBAUER Jiří KŘIVANOVÁ Andrea MAYER Jiří HÁJEK Roman

Year of publication 2010
Type Article in Periodical
Magazine / Source Vnitřní lékařství
MU Faculty or unit

Faculty of Medicine

Citation
Field Oncology and hematology
Keywords Langerhans cell histiocystosis; Erdheim-Chester disease; diabetes insipidus centralis
Description Central diabetes insipidus with an onset in adulthood is very rare. Unlike in children, central diabetes insipidus in adults is more frequently caused by inflammatory processes and neoplastic infiltrations that do not originate from the neuronal tissue than primary neuronal tissue tumours. Rare histiocytic neoplasias (Langerhans cell histiocytosis, xanthogranulomatosis and Erdheim-Chester disease) have a specific affinity to hypothalamus and the pituitary stalk not only in paediatric patients but also when occurring in adults. We describe 3 cases of central diabetes insipidus with an onset in adulthood.
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