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Pediatric endocrine surgery: a 20-year experience at the Mayo Clinic

Authors :
Yi Cai
L. X. Qiu
Clive S. Grant
Anna Kundel
Geoffrey B. Thompson
Aida N. Lteif
Peter J. Tebben
Siobhan T. Pittock
F. W. Schwenk
Melanie L. Richards
Seema Kumar
Ian D. Hay
Source :
The Journal of clinical endocrinology and metabolism. 99(2)
Publication Year :
2014

Abstract

Surgically managed endocrinopathies are rare in children. Most surgeons have limited experience in this field. Herein we report our operative experience with pediatric patients, performed over two decades by high-volume endocrine surgeons.The study was conducted at the Mayo Clinic (a tertiary referral center).Patients were19 years old and underwent an endocrine operation (1993-2012).Demographics, surgical procedure, diagnoses, morbidity, and mortality were retrospectively reviewed.A total of 241 primary cases included 177 thyroid procedures, 13 neck dissections, 24 parathyroidectomies, 14 adrenalectomies, 7 paragangliomas, and 6 pancreatic procedures. Average age of patients was 14.2 years. There were 133 total thyroidectomies and 40 hemithyroidectomies. Fifty-three cases underwent a central or lateral neck dissection. Six-month follow-up was available for 98 total thyroidectomy patients. There were four cases of permanent hypoparathyroidism (4%) and no permanent recurrent laryngeal nerve (RLN) paralyses. Sequelae of neck dissections included temporary RLN neurapraxia and Horner's syndrome. Parathyroidectomy was performed on 24 patients: 20 with primary hyperparathyroidism (HPT), three with tertiary HPT, and one with familial hypocalciuric hypocalcemia. Three patients (16%) had recurrent HPT, all with multiglandular disease. One patient had temporary RLN neurapraxia. We performed seven bilateral and seven unilateral adrenalectomies; eight were laparoscopic. Indications included pheochromocytoma, Cushing's syndrome, adrenocortical carcinoma, congenital adrenal hyperplasia, and ganglioneuroma. One death was due to adrenocortical carcinoma. Five paraganglioma patients had succinate dehydrogenase subunit B mutations, and one recurred. Six patients with insulinoma underwent enucleation (n = 5) or distal pancreatectomy (n = 1). A single postoperative abscess was managed nonoperatively.Pediatric endocrine procedures are uncommon but can be safely performed with complication rates comparable to those of the adult population. It is imperative that these operations be performed by high-volume surgeons.

Details

ISSN :
19457197
Volume :
99
Issue :
2
Database :
OpenAIRE
Journal :
The Journal of clinical endocrinology and metabolism
Accession number :
edsair.doi.dedup.....4608fcf6e3a7724cc158d2de76a85b1b