{"title":"Associated Coalitions of Tarsal Bones: Review of the Literature and Presentation of a Classification.","authors":"Amir Reza Vosoughi, Jacob Matz, Stefan Rammelt","doi":"10.5435/JAAOS-D-24-01191","DOIUrl":null,"url":null,"abstract":"<p><p>Associated coalitions of tarsal bones, either unilateral or bilateral, may be classified to developmental or syndromic types. There are no specific patterns for osseous or nonosseous configurations of associated tarsal coalitions. Associated developmental tarsal coalitions can be categorized into dual, threefold, massive, and total tarsal coalitions according to the number and sites of the involved joints. Dual coalitions are more common than other types. Among dual tarsal coalitions, the most frequent combination is talocalcaneal (TC) and calcaneonavicular coalitions, also referred to as double coalition, followed by combination of TC and talonavicular coalitions. The most frequent threefold coalition is the triple coalition, defined as concomitant TC, calcaneonavicular, and talonavicular coalitions. Massive tarsal coalition is defined as a nonsyndromic abnormality with involvement of more than three intertarsal joints or occurrence of a concomitant coalition outside the intertarsal joints, that is, tarsometatarsal joints and/or between metatarsal bases. Total tarsal coalition is the synostosis between all tarsal bones. Syndromic multiple tarsal coalition is a part of a hereditary complex skeletal malformation such as different phocomelia, craniosynostosis, and tarsal-carpal coalition syndromes. This literature review discusses associated coalitions, focusing on anatomical classification, workup, and treatment.</p>","PeriodicalId":51098,"journal":{"name":"Journal of the American Academy of Orthopaedic Surgeons","volume":" ","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Academy of Orthopaedic Surgeons","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.5435/JAAOS-D-24-01191","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ORTHOPEDICS","Score":null,"Total":0}
Associated Coalitions of Tarsal Bones: Review of the Literature and Presentation of a Classification.
Associated coalitions of tarsal bones, either unilateral or bilateral, may be classified to developmental or syndromic types. There are no specific patterns for osseous or nonosseous configurations of associated tarsal coalitions. Associated developmental tarsal coalitions can be categorized into dual, threefold, massive, and total tarsal coalitions according to the number and sites of the involved joints. Dual coalitions are more common than other types. Among dual tarsal coalitions, the most frequent combination is talocalcaneal (TC) and calcaneonavicular coalitions, also referred to as double coalition, followed by combination of TC and talonavicular coalitions. The most frequent threefold coalition is the triple coalition, defined as concomitant TC, calcaneonavicular, and talonavicular coalitions. Massive tarsal coalition is defined as a nonsyndromic abnormality with involvement of more than three intertarsal joints or occurrence of a concomitant coalition outside the intertarsal joints, that is, tarsometatarsal joints and/or between metatarsal bases. Total tarsal coalition is the synostosis between all tarsal bones. Syndromic multiple tarsal coalition is a part of a hereditary complex skeletal malformation such as different phocomelia, craniosynostosis, and tarsal-carpal coalition syndromes. This literature review discusses associated coalitions, focusing on anatomical classification, workup, and treatment.
期刊介绍:
The Journal of the American Academy of Orthopaedic Surgeons was established in the fall of 1993 by the Academy in response to its membership’s demand for a clinical review journal. Two issues were published the first year, followed by six issues yearly from 1994 through 2004. In September 2005, JAAOS began publishing monthly issues.
Each issue includes richly illustrated peer-reviewed articles focused on clinical diagnosis and management. Special features in each issue provide commentary on developments in pharmacotherapeutics, materials and techniques, and computer applications.