A Novel, Joint Sparing Surgical Approach to the Management of Giant Cell Tumor of the Distal Radius in a Pediatric Patient: A Case Report and Comprehensive Literature Review.
{"title":"A Novel, Joint Sparing Surgical Approach to the Management of Giant Cell Tumor of the Distal Radius in a Pediatric Patient: A Case Report and Comprehensive Literature Review.","authors":"Tushar Lalchandani, Lakshmana Das, Pankaj Sharma, Tarun Goyal, Nilesh Barwar","doi":"10.13107/jocr.2025.v15.i09.6028","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Giant cell tumor (GCT) of bone is a rare, locally aggressive neoplasm predominantly affecting skeletally mature individuals, with infrequent, uncommon occurrence in the pediatric population.</p><p><strong>Case report: </strong>This case report describes a young skeletally immature female presenting with a Campanacci grade 3 GCT of the distal radius, characterized an osteolytic lesion sparing the epiphysis. Following biopsy confirmation, the patient underwent wide local excision of the tumor with ulnar translocation, fixed using a distal radius locking plate to preserve joint integrity. Post-operative rehabilitation included physiotherapy to restore wrist mobility and grip strength.</p><p><strong>Results: </strong>At 2 years post-surgery, the patient demonstrated no re-occurrence of tumor and satisfactory functional outcomes, including 90° dorsiflexion, 35° palmar flexion, 60° pronosupination, and 68% grip strength compared to the contralateral side.</p><p><strong>Conclusion: </strong>This report highlights an innovative surgical approach that preserves joint functionality in pediatric GCT cases, emphasizing the importance of anatomical reconstruction and long-term functional restoration.</p>","PeriodicalId":16647,"journal":{"name":"Journal of Orthopaedic Case Reports","volume":"15 9","pages":"95-100"},"PeriodicalIF":0.0000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12422635/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Orthopaedic Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.13107/jocr.2025.v15.i09.6028","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Giant cell tumor (GCT) of bone is a rare, locally aggressive neoplasm predominantly affecting skeletally mature individuals, with infrequent, uncommon occurrence in the pediatric population.
Case report: This case report describes a young skeletally immature female presenting with a Campanacci grade 3 GCT of the distal radius, characterized an osteolytic lesion sparing the epiphysis. Following biopsy confirmation, the patient underwent wide local excision of the tumor with ulnar translocation, fixed using a distal radius locking plate to preserve joint integrity. Post-operative rehabilitation included physiotherapy to restore wrist mobility and grip strength.
Results: At 2 years post-surgery, the patient demonstrated no re-occurrence of tumor and satisfactory functional outcomes, including 90° dorsiflexion, 35° palmar flexion, 60° pronosupination, and 68% grip strength compared to the contralateral side.
Conclusion: This report highlights an innovative surgical approach that preserves joint functionality in pediatric GCT cases, emphasizing the importance of anatomical reconstruction and long-term functional restoration.