BACKGROUND Posterior ankle impingement syndrome (PAIS) is a cause of ankle pain due to pinching of bony or soft tissue structures in the hindfoot. The diagnosis is primarily made based on detailed history and accurate clinical examination. The delay in its diagnosis has not yet been described in the pediatric and adolescent population. AIM To identify and characterize misdiagnosed cases of PAIS in pediatric and adolescent patients. METHODS This descriptive prospective study at a tertiary children's hospital included patients <= 18 years who underwent posterior ankle arthroscopy after presenting with chronic posterior ankle pain after being diagnosed with PAIS. Collected data included: Demographics, prior diagnoses and treatments, providers seen, time to diagnosis from presentation, and prior imaging obtained. Visual Analogue Scale (VAS) for pain and American Orthopedic Foot Ankle Society (AOFAS) ankle-hindfoot scores were noted at initial presentation and follow-up. RESULTS 35 patients (46 ankles) with average age of 13 years had an average 19 mo (range 0-60 mo) delay in diagnosis from initial presentation. 25 (71%) patients had previously seen multiple medical providers and were given multiple other diagnoses. All 46 (100%) ankles had tenderness to palpation over the posterior ankle joint. Radiographs were reported normal in 31/42 (72%) exams. In 32 ankles who underwent MRI, the most common findings included os trigonum (47%)/Stieda process (47%). Conservative treatment had already been attempted in all patients. Ankle impingement pathology was confirmed during arthroscopy in 46 (100%) ankles. At an average follow-up of 13.1 mo, there was an improvement of VAS (pre-op 7.0 to post-op 1.2) and AOFAS scores (pre-op 65.1 to post-op 94). CONCLUSION This is the first study which shows that PAIS is a clinically misdiagnosed cause of posterior ankle pain in pediatric and adolescent population; an increased awareness about this diagnosis is needed amongst providers treating young patients.
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Cambridge Hlth Alliance, Podiatr Surg, Cambridge, MA 02139 USA
Harvard Med Sch, 1439 Cambridge St, Cambridge, MA 02139 USACambridge Hlth Alliance, Podiatr Surg, Cambridge, MA 02139 USA
Theodoulou, Michael H.
Ravine, Madison
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Cambridge Hlth Alliance, Podiatr Med & Surg Residency Program, 1439 Cambridge St, Cambridge, MA 02139 USACambridge Hlth Alliance, Podiatr Surg, Cambridge, MA 02139 USA
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St Vincents & Mercy Private Hosp, Orthopaed Res Unit, Melbourne, Vic 3002, AustraliaSt Vincents & Mercy Private Hosp, Orthopaed Res Unit, Melbourne, Vic 3002, Australia
Henderson, I
La Valette, D
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St Vincents & Mercy Private Hosp, Orthopaed Res Unit, Melbourne, Vic 3002, AustraliaSt Vincents & Mercy Private Hosp, Orthopaed Res Unit, Melbourne, Vic 3002, Australia
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Palo Alto Med Fdn, 701 E EL Camino Real, Mountain View, CA 94040 USAPalo Alto Med Fdn, 701 E EL Camino Real, Mountain View, CA 94040 USA
Ishibashi, Megan A.
Doyle, Matthew D.
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Palo Alto Med Fdn, 701 E EL Camino Real, Mountain View, CA 94040 USAPalo Alto Med Fdn, 701 E EL Camino Real, Mountain View, CA 94040 USA
Doyle, Matthew D.
Krcal Jr, Craig E.
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Kaiser San Francisco Bay Area Foot & Ankle Residen, 3600 Broadway, Oakland, CA 94611 USAPalo Alto Med Fdn, 701 E EL Camino Real, Mountain View, CA 94040 USA
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Chelsea & Westminster Hosp, Dept Radiol, London SW10 9NH, EnglandChelsea & Westminster Hosp, Dept Radiol, London SW10 9NH, England
Lee, Justin C.
Calder, James D. F.
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Univ London Imperial Coll Sci Technol & Med, London, EnglandChelsea & Westminster Hosp, Dept Radiol, London SW10 9NH, England
Calder, James D. F.
Healy, Jeremiah C.
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Chelsea & Westminster Hosp, Dept Radiol, London SW10 9NH, England
Univ London Imperial Coll Sci Technol & Med, London, EnglandChelsea & Westminster Hosp, Dept Radiol, London SW10 9NH, England