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Parathyroidectomy in the Treatment of Childhood Hyperparathyroidism

A Single-Institution Experience

Bibliographic Data

ID15714818
AuthorsSeyithan Özaydin (0000-0003-1964-903X, Bahçeşehir University, corresponding author), Serkan Volkan SARI (Sağlık Bilimleri Üniversitesi), Serkan Sari (0000-0003-2918-1776, Department of General Surgery, Basaksehir Cam and City Hospital, University of Health Sciences, Istanbul 34480, Turkey), Emel Hatun Aytaç Kaplan (0000-0002-8385-4049, University of Health Science), Zümrüt Kocabey Sütçü (0000-0001-7335-1272, University of Health Science), Sevgi Yavuz (0000-0002-0053-6986, University of Health Science), Hamit Yücel Barut (0000-0002-6004-9194, University of Health Science), Huseyin Karatay (0000-0002-4217-2834, University of Health Science), Burcu Esen Akkaş (0000-0001-6623-1600, University of Health Science)
Year2025
Volume13
Issue1
Pages64-64
Publication date2025-12-31
Open AccessYes
TypeARTICLE
VenueChildren (JOURNAL)
Journal identifiersISSN: 2227-9067 • E-ISSN: 2227-9067
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/children13010064
PMID41597072
OpenAlexW7117787840
LanguageEN
References cited31

Purpose: Hyperparathyroidism (HPT) is a condition marked by excessive secretion of parathyroid hormone (PTH), leading to disturbances in calcium, phosphate, and vitamin D metabolism. HPT is classified into primary (pHPT), secondary (sHPT), and tertiary (tHPT) types, which can cause systemic complications. Parathyroidectomy (PTX) remains the cornerstone treatment for pHPT and refractory cases of sHPT and tHPT. Methods: A retrospective review was conducted on 10 pediatric patients who underwent PTX for HPT at our clinic between 2016 and 2024. Demographic data, preoperative imaging, laboratory findings, surgical details, pathology reports, and postoperative outcomes were analyzed. Patients were categorized as having either pHPT ( n = 6) or renal HPT (r-HPT; n = 4), which included one case of sHPT and three cases of tHPT. Results: The mean age of pHPT and r-HPT patients was 15 and 13 years, respectively. While 50% of pHPT patients were female, all r-HPT patients were female. Preoperative imaging localized parathyroid lesions using ultrasonography in all cases, but Sestamibi scintigraphy had a lower detection rate (66.7%). Minimally invasive parathyroidectomy was performed in single-gland pHPT cases, while bilateral neck exploration was used for multiglandular pHPT and all r-HPT cases. No intraoperative complications were observed. Postoperatively, all patients demonstrated normalized calcium, phosphate, and PTH levels with significant symptomatic improvement. Hungry bone syndrome developed in one r-HPT patient and was managed successfully. No recurrences were noted during an average follow-up of 39 months. Conclusions: PTX is a safe and effective treatment for pediatric HPT, providing excellent biochemical and clinical outcomes. Multidisciplinary collaboration is crucial in managing pediatric cases, particularly those with complex renal HPT

Hyperparathyroidism · Parathyroid hormone · Parathyroidectomy · Primary hyperparathyroidism · Retrospective cohort study · Secondary hyperparathyroidism · Tertiary hyperparathyroidism · Parathyroid Disorders and Treatments · Thyroid and Parathyroid Surgery · Vitamin D Research Studies

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