An exceptionally rare case of Cushing’s syndrome caused by ectopic ACTH syndrome due to olfactory neuroblastoma in childhood
Author:
Affiliation:
1. Division of Pediatric Endocrinology , School of Medicine, Pamukkale University , Denizli , Türkiye
2. Division of Pathology , Pamukkale University, School of Medicine , Denizli , Türkiye
Abstract
Publisher
Walter de Gruyter GmbH
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health
Link
https://www.degruyter.com/document/doi/10.1515/jpem-2022-0506/pdf
Reference10 articles.
1. Stratakis, CA. An update on Cushing syndrome in pediatrics. Ann Endocrinol 2018;79:125–31.
2. More, J, Young, J, Reznik, Y, Raverot, G, Borson-Chazot, F, Rohmer, V, et al.. Groupe Français des Tumeurs Endocrines (GTE). J Clin Endocrinol Metab 2011;96:1213–22. https://doi.org/10.1210/jc.2010-2276.
3. Kunc, M, Gabrych, A, Czapiewski, P, Sworczak, K. Paraneoplastic syndromes in olfactory neuroblastoma. Contemp Oncol 2015;19:6–16. https://doi.org/10.5114/wo.2015.46283.
4. Galioto, S, Petrillo, AD, Pastori, M, Arecchi, A. Metastatic esthesioneuroblastoma secreting adrenocorticotropic hormone in pediatric patients. J Craniofac Surg 2011;22:1924–9. https://doi.org/10.1097/scs.0b013e318210bce4.
5. Fiani, B, Quadri, SA, Cathel, A, Farooqui, M, Ramachandran, A, Siddiqi, I, et al.. Esthesioneuroblastoma: a comprehensive review of diagnosis, management, and current treatment options. World Neurosurg 2019;126:194–211. https://doi.org/10.1016/j.wneu.2019.03.014.
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