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Evaluation of the etiological and clinical characteristics of pediatric central diabetes insipidus

  • Elnare Gasimova , Merih Berberoğlu , Elif Özsu ORCID logo EMAIL logo , Zehra Aycan , Rukiye Uyanık , Esra Bilici , Ayşegül Ceran and Zeynep Şiklar
Published/Copyright: July 12, 2022

Abstract

Objectives

Central diabetes insipidus (CDI) is a rare but important disease of varying etiology that poses challenges in diagnosis and follow-up. Identifying diagnostic difficulties in patients with CDI will help ensure an optimal approach to their management and follow-up. This study aimed to characterize the clinical and etiological characteristics of CDI in pediatric patients.

Methods

We analyzed the admission and follow-up data of CDI patients aged 0–18 years who were followed in our center between 2010 and 2019.

Results

The study included 56 patients with a mean age at diagnosis of 7.92 ± 5.11 years and symptom duration of 8.65 ± 21.3 months. The patients were grouped by etiology into those with organic causes, such as structural anomalies, tumors, and trauma (group 1, n=41) and other causes (group 2, n=15). The prevalence of idiopathic CDI was 16%. At least one pituitary hormone deficiency was detected in 60.7%, the most common being thyroid stimulating hormone deficiency. Patients in group 1 had a higher mean age at diagnosis, shorter symptom duration, and higher frequency of other pituitary hormone deficiencies compared to group 2. Additionally, germinoma was detected 1 year subsequent to normal MRI findings at diagnosis and another patient was diagnosed with Langerhans cell histiocytosis (LCH) 5 years after diagnosis. All patients responded well to replacement therapies, but two patients with germinoma died during follow-up.

Conclusions

In the pediatric age group, intracranial organic pathologies are an important etiology of CDI, and despite a short symptomatic period, determining the cause may be challenging and prolonged. Patients presenting at a young age with a long history of symptoms and no other pituitary hormone deficiency are unlikely to have organic CDI. However, organic causes such as LCH should be evaluated at all ages. Patients with idiopathic disease are candidates for further etiological studies, and repeated cranial imaging is important during follow-up.


Corresponding author: Associate Prof. Elif Ozsu, MD, Department of Pediatric Endocrinology and Diabetes, Ankara Univesity School of Medicine, Balkiraz Mahallesi, Tıp Fakültesi Caddesi No: 1/4, 06620, Mamak, Ankara, Turkey, Phone: +90 505 454 75 89, Fax: +90 312 319 82 36, E-mail:

  1. Research funding: None declared.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: The local Institutional Review Board deemed the study exempt from review.

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Received: 2022-01-31
Accepted: 2022-06-20
Published Online: 2022-07-12
Published in Print: 2022-08-26

© 2022 Walter de Gruyter GmbH, Berlin/Boston

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