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Surgical treatment of children with hyperparathyroidism: Single centre experience

Abstract Background Hyperparathyroidism (HPT) in children is rare and surgical management is supported only by limited evidence. Methods Retrospective case series of all children under the age of 16 years who underwent parathyroidectomy (PTx) between 1978 and 2012. Results We identified 29 children...

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Bibliographic Details
Published in:Journal of pediatric surgery 2014-11, Vol.49 (11), p.1539-1543
Main Authors: Alagaratnam, S, Brain, C, Spoudeas, H, Dattani, M.T, Hindmarsh, P, Allgrove, J, Van’t Hoff, W, Kurzawinski, T.R
Format: Article
Language:English
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Summary:Abstract Background Hyperparathyroidism (HPT) in children is rare and surgical management is supported only by limited evidence. Methods Retrospective case series of all children under the age of 16 years who underwent parathyroidectomy (PTx) between 1978 and 2012. Results We identified 29 children who had surgery for HPT. Six were neonates with neonatal severe hyperparathyroidism (NSHPT) and 23 older children (age range 7–16 years) with sporadic (16) or familial (7) HPT and 93% were symptomatic. Accuracy of ultrasound and MIbi in localising solitary parathyroid adenomas was 96%, but less helpful in hyperplasia and neonates. Children with NSHPT underwent 5 curative total and 1 subtotal PTx (no reoperations). Children with familial HPT underwent 3 total and 4 subtotal PTx. One child with subtotal PTx required a reoperation. Children with sporadic HPT underwent subtotal PTx prior to 1980 (2), exploration and removal of enlarged glands 1980–2002 (5) and minimally invasive PTx since 2002 (9) and all cured by the first operation. Conclusions Our study documents that HPT in children is predominantly symptomatic on presentation and genetically determined in 46% of cases. Imaging is accurate in localising parathyroid adenomas, but not hyperplasias. Total PTx for familial HPT was curative and minimally invasive PTx is the operation of choice for older children with sporadic HPT.
ISSN:0022-3468
1531-5037
DOI:10.1016/j.jpedsurg.2014.05.032