Congenital Bilateral Complete Agenesis of the Hallucal Sesamoids: A Case Report

Journal of chiropractic medicine Pub Date : 2025-01-01 Epub Date: 2025-09-24 DOI:10.1016/j.jcm.2025.08.016
Dingbo Shi DC , Aidan E. O’Brien DC , Jesse D. Politowski DC , Norman W. Kettner DC
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Abstract

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.
先天性双侧幻觉籽状体完全缺失1例
目的报告一例双侧完全性幻觉海马发育不全的病例。临床特征:23岁女性,左侧第4跖骨头部疼痛,早晨加重,无法跑步。一周后,她在打橄榄球时右脚内翻受伤。干预措施和结果:x线摄影显示双侧完全没有骨性幻觉性籽状瘤,第一跖骨头圆形,无特征,没有籽状沟,也没有籽状嵴,后来在超声检查中证实缺乏纤维软骨淋巴结。结论双侧幻觉籽突完全发育不全是罕见的。本研究报告一例无症状的先天性双侧幻觉性籽状体完全性发育不全,其影像学表现及超声检查证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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