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      An adolescent girl with syndrome of inappropriate antidiuretic hormone secretion preceding the diagnosis of olfactory neuroblastoma – a case report

      case-report

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          Abstract

          Objectives

          We present an adolescent in whom olfactory neuroblastoma (ONB) was detected on follow-up magnetic resonance imaging (MRI) 2.5 years after SIADH diagnosis. Our case contrasts prior pediatric reports in which ONB and SIADH were diagnosed concurrently.

          Case presentation

          A previously healthy 13-year-old girl was found to have SIADH during evaluation for restrictive eating. Work-up ruled out adrenal, thyroid and paraneoplastic causes, diuretic use, and vasopressin receptor and aquaporin channel mutations. Brain MRI was normal except for paranasal sinus (PNS) inflammatory changes to the left fronto-maxillary sinuses and frontoethmoidal recess. The sodium levels normalized with fluid restriction (800-900 ml/m 2/day). Multiple repeated attempts to liberalize fluid intake resulted in recurrent hyponatremia. Follow-up brain MRIs 4 and 11 months after the initial presentation showed persistent PNS inflammatory changes. A subsequent brain MRI 31 months after initial presentation demonstrated a lesion in the left frontoethmoidal recess extending into the left nasal cavity and biopsy showed low grade ONB. The patient underwent surgery with normalization of serum sodium on liberalized fluid intake. Seven days after surgery, she had recurrence of SIADH, and brain MRI showed remnant of the ONB at the fovea ethmoidalis. She completed adjuvant radiotherapy though her SIADH persisted.

          Conclusions

          Our case highlights the importance of considering ONB in the evaluation of children with SIADH. Idiopathic SIADH is rare in children and if no cause is identified, computed tomography of sinuses and nasal endoscopy should be considered earlier in the work-up of these patients, particularly in the absence of sinus symptoms.

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          Most cited references15

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          Diagnosis, evaluation, and treatment of hyponatremia: expert panel recommendations.

          Hyponatremia is a serious, but often overlooked, electrolyte imbalance that has been independently associated with a wide range of deleterious changes involving many different body systems. Untreated acute hyponatremia can cause substantial morbidity and mortality as a result of osmotically induced cerebral edema, and excessively rapid correction of chronic hyponatremia can cause severe neurologic impairment and death as a result of osmotic demyelination. The diverse etiologies and comorbidities associated with hyponatremia pose substantial challenges in managing this disorder. In 2007, a panel of experts in hyponatremia convened to develop the Hyponatremia Treatment Guidelines 2007: Expert Panel Recommendations that defined strategies for clinicians caring for patients with hyponatremia. In the 6 years since the publication of that document, the field has seen several notable developments, including new evidence on morbidities and complications associated with hyponatremia, the importance of treating mild to moderate hyponatremia, and the efficacy and safety of vasopressin receptor antagonist therapy for hyponatremic patients. Therefore, additional guidance was deemed necessary and a panel of hyponatremia experts (which included all of the original panel members) was convened to update the previous recommendations for optimal current management of this disorder. The updated expert panel recommendations in this document represent recommended approaches for multiple etiologies of hyponatremia that are based on both consensus opinions of experts in hyponatremia and the most recent published data in this field. Copyright © 2013 Elsevier Inc. All rights reserved.
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            Esthesioneuroblastoma recurrence presenting as a syndrome of inappropriate antidiuretic hormone secretion

              • Record: found
              • Abstract: found
              • Article: not found

              Malignancy associated SIADH: Characterization and clinical implications.

              To determine the distribution of etiologies for the syndrome of inappropriate antidiuretic hormone secretion (SIADH) in hospitalized patients with active malignancies and to characterize them according to the different etiologies.

                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/2765199Role: Role: Role: Role: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/1525155Role: Role: Role: Role: Role: Role:
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                Role: Role: Role: Role: Role: Role:
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                URI : https://loop.frontiersin.org/people/982373Role: Role: Role: Role: Role: Role: Role:
                Journal
                Front Endocrinol (Lausanne)
                Front Endocrinol (Lausanne)
                Front. Endocrinol.
                Frontiers in Endocrinology
                Frontiers Media S.A.
                1664-2392
                16 October 2024
                2024
                : 15
                : 1447685
                Affiliations
                [1] 1 Division of Pediatric Endocrinology, Department of Pediatrics, Hasbro Children’s Hospital , Providence, RI, United States
                [2] 2 The Warren Alpert Medical School of Brown University , Providence, RI, United States
                [3] 3 Department of Pediatrics, Center for Endocrinology, Diabetes and Metabolism, Children’s Hospital Los Angeles, Department of Pediatrics, Keck School of Medicine, University of Southern California , Los Angeles, CA, United States
                [4] 4 Department of Diagnostic Imaging, Rhode Island Hospital , Providence, RI, United States
                [5] 5 Division of Pediatric Otolaryngology, Department of Surgery, Hasbro Children's Hospital , Providence, RI, United States
                [6] 6 Division of Pediatric Hematology-Oncology, Department of Pediatrics, Hasbro Children’s Hospital , Providence, RI, United States
                [7] 7 Division of Pediatric Nephrology and Hypertension, Department of Pediatrics, Hasbro Children’s Hospital , Providence, RI, United States
                Author notes

                Edited by: Rodolfo A. Rey, Hospital de Niños Ricardo Gutiérrez, Argentina

                Reviewed by: Anna Arecco, University of Genova, Italy

                Sebastian Castro, CONICET Centro de Investigaciones Endocrinológicas “Dr. César Bergadá” (CEDIE), Argentina

                *Correspondence: Monica Serrano-Gonzalez, monica_serrano@ 123456brown.edu
                Article
                10.3389/fendo.2024.1447685
                11521841
                39479268
                ecf700df-5d2b-487b-831a-1ff8e919c84d
                Copyright © 2024 Sasidharan Pillai, Boxerman, Groblewski, DeNardo, Faizan, Topor, Robilliard and Serrano-Gonzalez

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 12 June 2024
                : 27 September 2024
                Page count
                Figures: 1, Tables: 2, Equations: 0, References: 15, Pages: 6, Words: 2476
                Funding
                The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.
                Categories
                Endocrinology
                Case Report
                Custom metadata
                Pediatric Endocrinology

                Endocrinology & Diabetes
                adolescents,children,olfactory neuroblastoma,esthesioneuroblastoma,siadh,hyponatremia,antidiuretic hormone,eating disorder

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