A Rare Case of Central Diabetes Insipidus in a Pediatric Patient
-
Published:2024-07-01
Issue:7-8
Volume:37
Page:577-578
-
ISSN:1646-0758
-
Container-title:Acta Médica Portuguesa
-
language:
-
Short-container-title:Acta Med Port
Author:
Henriques Ana Raquel, M. Lopes MiguelORCID, Robalo Brígida, Pereira Carla, Sampaio Maria de Lurdes
Publisher
Ordem dos Medicos
Reference5 articles.
1. Schaefers J, Cools M, De Waele K, Gies I, Beauloye V, Lysy P, et al. Clinical presentation and outcome of children with central diabetes insipidus associated with a self-limited or transient pituitary stalk thickening, diagnosed as infundibuloneurohypophysitis. Clin Endocrinol. 2017;87:171-6. 2. Morota K, Tadokoro H, Sawano K, Watanabe K, Iwata N, Fujisawa H, et al. A 7-year-old boy with central diabetes insipidus presenting with thickened pituitary stalk and anti-rabphilin-3A antibody positivity. J Pediatr Endocrinol Metab. 2022;35:687-90. 3. Johnston PC, Chew LS, Hamrahian AH, Kennedy L. Lymphocytic infundibulo-neurohypophysitis: a clinical overview. Endocrine. 2015;50:531-6. 4. Moszczyńska E, Kunecka K, Baszyńska-Wilk M, Perek-Polnik M, Majak D, Grajkowska W. Pituitary stalk thickening: causes and consequences. the children’s memorial health institute experience and literature review. Front Endocrinol. 2022;13:868558. 5. Donegan D, Saeed Z, Delivanis DA, Murad MH, Honegger J, Amereller F, et al. Outcomes of initial management strategies in patients with autoimmune lymphocytic hypophysitis: a systematic review and meta- analysis. J Clin Endocrinol Metab. 2022;107:1170-90.
|
|