Pediatric Endocrine Surgery: A 20-Year Experience at the Mayo Clinic

被引:70
作者
Kundel, A. [1 ]
Thompson, G. B. [1 ]
Richards, M. L. [1 ]
Qiu, L. X. [1 ]
Cai, Y. [1 ]
Schwenk, F. W. [1 ]
Lteif, A. N. [1 ]
Pittock, S. T. [1 ]
Kumar, S. [1 ]
Tebben, P. J. [1 ]
Hay, I. D. [1 ]
Grant, C. S. [1 ]
机构
[1] Mayo Clin, Rochester, MN 55905 USA
关键词
PRIMARY HYPERPARATHYROIDISM; ECONOMIC OUTCOMES; THYROID-CARCINOMA; CHILDREN; VOLUME; CANCER; COMPLICATIONS; PREDICTORS; SPECIALTY; MORBIDITY;
D O I
10.1210/jc.2013-2617
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: 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. Setting: The study was conducted at the Mayo Clinic (a tertiary referral center). Patients: Patients were < 19 years old and underwent an endocrine operation (1993-2012). Main Outcome Measures: Demographics, surgical procedure, diagnoses, morbidity, and mortality were retrospectively reviewed. Results: 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. Conclusion: 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.
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页码:399 / 406
页数:8
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