Journal of chiropractic medicine · 2025
Congenital Bilateral Complete Agenesis of the Hallucal Sesamoids: A Case Report.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Shi Dingbo, O'Brien Aidan E, Politowski Jesse D, Kettner Norman W
Аннотация
OBJECTIVE: The purpose of this case report is to describe a patient with bilateral complete hallucal sesamoidal agenesis.
CLINICAL FEATURES: A 23 year-old female presented with left 4th metatarsal head pain that is worse in the morning and prevents her from running. A week later, she had an inversion injury in the right foot while playing flag football.
INTERVENTIONS AND OUTCOMES: Radiography incidentally demonstrated bilateral complete absence of osseous hallucal sesamoids with a round, featureless 1st metatarsal head that does not have sesamoidal grooves nor an intersesamoidal crest and later confirmed lack of fibrocartilaginous nodes on ultrasonography.
CONCLUSION: Bilateral complete agenesis of the hallucal sesamoids is rare. This study describes a case of asymptomatic congenital bilateral complete agenesis of the hallucal sesamoids visualized on radiography and confirmed with ultrasonography.
CLINICAL FEATURES: A 23 year-old female presented with left 4th metatarsal head pain that is worse in the morning and prevents her from running. A week later, she had an inversion injury in the right foot while playing flag football.
INTERVENTIONS AND OUTCOMES: Radiography incidentally demonstrated bilateral complete absence of osseous hallucal sesamoids with a round, featureless 1st metatarsal head that does not have sesamoidal grooves nor an intersesamoidal crest and later confirmed lack of fibrocartilaginous nodes on ultrasonography.
CONCLUSION: Bilateral complete agenesis of the hallucal sesamoids is rare. This study describes a case of asymptomatic congenital bilateral complete agenesis of the hallucal sesamoids visualized on radiography and confirmed with ultrasonography.