{"title":"Chronic Midfoot Pain Due to Idiopathic Osteonecrosis of Tarsal Navicular Bone in Adult - Mueller-Weiss Syndrome: A Case Report.","authors":"N Adithya, P Sunil Kumar, B S Narendra, V Varun","doi":"10.13107/jocr.2025.v15.i02.5228","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Mueller-Weiss syndrome is a rare condition seen in adults due to spontaneous osteonecrosis of tarsal navicular bone unlike Koehler's disease which is quite common in paediatric population.</p><p><strong>Case report: </strong>We report a single case of Mueller-Weiss syndrome in an adult female. After a trail of conservative treatment, operative management was done with excision of necrotic fragment and arthrodesis of mid-foot joints augmented with tricortical iliac crest graft. Good fusion and significant reduction of pain on weight-bearing was observed after a duration of 6 weeks.</p><p><strong>Conclusion: </strong>Mueller-Weiss syndrome is relatively rare differential for mid-foot pain in adult population. Early recognition and management of the condition prevents arthritic changes and disability.</p>","PeriodicalId":16647,"journal":{"name":"Journal of Orthopaedic Case Reports","volume":"15 2","pages":"60-64"},"PeriodicalIF":0.0000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11823864/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.i02.5228","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: Mueller-Weiss syndrome is a rare condition seen in adults due to spontaneous osteonecrosis of tarsal navicular bone unlike Koehler's disease which is quite common in paediatric population.
Case report: We report a single case of Mueller-Weiss syndrome in an adult female. After a trail of conservative treatment, operative management was done with excision of necrotic fragment and arthrodesis of mid-foot joints augmented with tricortical iliac crest graft. Good fusion and significant reduction of pain on weight-bearing was observed after a duration of 6 weeks.
Conclusion: Mueller-Weiss syndrome is relatively rare differential for mid-foot pain in adult population. Early recognition and management of the condition prevents arthritic changes and disability.