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Biology and Technology in the Surgical Treatment of Malignant Bone Tumours in Children and Adolescents, with a Special Note on the Very Young

Overview
Journal J Child Orthop
Publisher Sage Publications
Specialty Pediatrics
Date 2021 Sep 3
PMID 34476021
Citations 3
Authors
Affiliations
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Abstract

Purpose: The main challenge in reconstruction after malignant bone tumour resection in young children remains how and when growth-plates can be preserved and which options remain if impossible.

Methods: We describe different strategies to assure best possible long-term function for young children undergoing resection of malignant bone tumours.

Results: Different resources are available to treat children with malignant bones tumours: a) preoperative planning simulates scenarios for tumour resection and limb reconstruction, facilitating decision-making for surgical and reconstructive techniques in individual patients; b) allograft reconstruction offers bone-stock preservation for future needs. Most allografts are intact at long-term follow-up, but limb-length inequalities and corrective/revision surgery are common in young patients; c) free vascularized fibula can be used as stand-alone reconstruction, vascularized augmentation of structural allograft or devitalized autograft. Longitudinal growth and joint remodelling potential can be preserved, if transferred with vascularized proximal physis; d) epiphysiolysis before resection with continuous physeal distraction provides safe resection margins and maintains growth-plate and epiphysis; e) 3D printing may facilitate joint salvage by reconstruction with patient-specific instruments. Very short stems can be created for fixation in (epi-)metaphysis, preserving native joints; f) growing endoprosthesis can provide for remaining growth after resection of epi-metaphyseal tumours. At ten-year follow-up, limb survival was 89%, but multiple surgeries are often required; g) rotationplasty and amputation should be considered if limb salvage is impossible and/or would result in decreased function and quality of life.

Conclusion: Several biological and technological reconstruction options must be merged and used to yield best outcomes when treating young children with malignant bone tumours.

Level Of Evidence: Level V Expert opinion.

Citing Articles

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What Do We Know about Survival in Skeletally Premature Children Aged 0 to 10 Years with Ewing Sarcoma? A Multicenter 10-Year Follow-Up Study in 60 Patients.

Bosma S, Van der Heijden L, Sierrasesumaga L, Merks H, Haveman L, van de Sande M Cancers (Basel). 2022; 14(6).

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A Reassessment of the Barrier Effect of the Physis against Metaphyseal Osteosarcoma: A Comprehensive Pathological Study with Its Radiological and Clinical Follow-Up Correlations.

Idoate M, Aquerreta J, Lamo-Espinosa J, San-Julian M Diagnostics (Basel). 2022; 12(2).

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Malignant bone tumours in children: What's up?.

Alves C J Child Orthop. 2021; 15(4):310-311.

PMID: 34476019 PMC: 8381390. DOI: 10.1302/1863-2548.15.210123.

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