{"title":"Tibial Plateau Fracture in a Patient with Fibular Hemimelia: A Case Report.","authors":"L Warnau, S Koulischer, V Bobu, S Y Maatou","doi":"10.13107/jocr.2026.v16.i10.8228","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Fibular hemimelia (FH) is the most common congenital longitudinal deficiency of the lower limb, characterized by partial or complete fibular absence and associated musculoskeletal abnormalities. Its coexistence with a traumatic tibial plateau fracture has not been previously reported in the literature. We present the first reported case of a comminuted bicondylar tibial plateau fracture occurring in a patient with complete congenital fibular absence and describe the specific anatomical and technical challenges encountered during surgical management.</p><p><strong>Case report: </strong>A 37-year-old Portuguese man with congenital right-sided FH (Achterman and Kalamchi type II) sustained a comminuted Schatzker V tibial plateau fracture following a fall from an electric scooter. Staged management consisted of temporary external fixation followed by dual-plate open reduction and internal fixation. The congenitally altered proximal tibial geometry necessitated the use of a contralateral implant, as the standard ipsilateral plate did not conform adequately. Post-operative recovery was complicated by delayed union of the posteromedial fragment, complex regional pain syndrome, and a complete rupture of the anterior cruciate ligament of indeterminate origin. At 4 years of follow-up, the patient had persistent knee stiffness with flexion limited to 100°, early post-traumatic gonarthrosis, and ambulated with a single crutch.</p><p><strong>Conclusion: </strong>Congenital fibular absence alters proximal tibial anatomy and neurovascular landmarks, complicating fracture fixation and requiring individualized surgical planning. However, the guarded long-term outcome and multiple confounding factors in this single case indicate that these anatomical observations should inform surgical vigilance rather than be generalized as a management protocol.</p>","PeriodicalId":16647,"journal":{"name":"Journal of Orthopaedic Case Reports","volume":"16 10","pages":"180-185"},"PeriodicalIF":0.0000,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13646565/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Orthopaedic Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.13107/jocr.2026.v16.i10.8228","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract
Introduction: Fibular hemimelia (FH) is the most common congenital longitudinal deficiency of the lower limb, characterized by partial or complete fibular absence and associated musculoskeletal abnormalities. Its coexistence with a traumatic tibial plateau fracture has not been previously reported in the literature. We present the first reported case of a comminuted bicondylar tibial plateau fracture occurring in a patient with complete congenital fibular absence and describe the specific anatomical and technical challenges encountered during surgical management.
Case report: A 37-year-old Portuguese man with congenital right-sided FH (Achterman and Kalamchi type II) sustained a comminuted Schatzker V tibial plateau fracture following a fall from an electric scooter. Staged management consisted of temporary external fixation followed by dual-plate open reduction and internal fixation. The congenitally altered proximal tibial geometry necessitated the use of a contralateral implant, as the standard ipsilateral plate did not conform adequately. Post-operative recovery was complicated by delayed union of the posteromedial fragment, complex regional pain syndrome, and a complete rupture of the anterior cruciate ligament of indeterminate origin. At 4 years of follow-up, the patient had persistent knee stiffness with flexion limited to 100°, early post-traumatic gonarthrosis, and ambulated with a single crutch.
Conclusion: Congenital fibular absence alters proximal tibial anatomy and neurovascular landmarks, complicating fracture fixation and requiring individualized surgical planning. However, the guarded long-term outcome and multiple confounding factors in this single case indicate that these anatomical observations should inform surgical vigilance rather than be generalized as a management protocol.