Journal of Pediatric Biochemistry 2010; 01(04): 289-296
DOI: 10.1055/s-0036-1586385
Review Article
Georg Thieme Verlag KG Stuttgart – New York

Management of sodium metabolism derangements in children treated for hypothalamic-hypophyseal tumors

Autoren

  • Patrizia Matarazzo

    a   Department of Pediatric Endocrinology and Diabetology, Regina Margherita Children Hospital, University of Torino, Torino, Italy
  • Gerdi Tuli

    a   Department of Pediatric Endocrinology and Diabetology, Regina Margherita Children Hospital, University of Torino, Torino, Italy
  • Francesca Verna

    a   Department of Pediatric Endocrinology and Diabetology, Regina Margherita Children Hospital, University of Torino, Torino, Italy
  • Daniele Tessaris

    a   Department of Pediatric Endocrinology and Diabetology, Regina Margherita Children Hospital, University of Torino, Torino, Italy
  • Ludovica Fiore

    a   Department of Pediatric Endocrinology and Diabetology, Regina Margherita Children Hospital, University of Torino, Torino, Italy
  • Alessandro Mussa

    a   Department of Pediatric Endocrinology and Diabetology, Regina Margherita Children Hospital, University of Torino, Torino, Italy
  • Marialia Repici

    a   Department of Pediatric Endocrinology and Diabetology, Regina Margherita Children Hospital, University of Torino, Torino, Italy
  • Roberto Lala

    a   Department of Pediatric Endocrinology and Diabetology, Regina Margherita Children Hospital, University of Torino, Torino, Italy

Verantwortlicher Herausgeber dieser Rubrik:
Weitere Informationen

Publikationsverlauf

26. Oktober 2010

05. Januar 2011

Publikationsdatum:
01. August 2016 (online)

Abstract

Hyponatremia and hypernatremia, common electrolyte abnormalities in children hospitalized for intracranial diseases, are life-threatening events. Diagnosis and adequate treatment of hypo- and hypernatremia are mandatory to prevent neurological sequelae. We report ante-and post-hypophyseal dysfunctions, disabilities and acute sodium metabolism derangements in 16 children affected by hypothalamic-hypophyseal tumors treated by neurosurgery and/or chemotherapy during a long-lasting follow-up. We compare acute hypo- and hypernatremic episodes during surgery between these patients, treated with a specific hormonal and infusive protocol (protocol A), and a previous cohort of patients, affected by similar tumors, treated with a previously published protocol (protocol B). All patients showed multiple or isolated pituitary dysfunctions and disabilities before chemotherapy and/or surgical treatment that worsened during the follow-up period. We found a statistical significant decrease of hyponatremic intra-operative acute events in children treated with protocol A. Sodium metabolism derangements complicating the course of hypothalamic-hypophyseal tumors can be partially prevented with specific per-operative protocols. Aim of this study is to present a new sodium metabolism derangements management in children treated for hypothalamic-hypophyseal tumors and to compare this with a previous one.