Incidental Finding of Unilateral Tensor Fascia Lata Agenesis in a Marathon Runner: An Unreported Phenomenon.

IF 3.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Tommaso Bellini, Claudio Bruno, Giacomo Brisca
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引用次数: 0

Abstract

Congenital agenesis of the tensor fascia lata (TFL) muscle is an extremely rare anomaly, with very few reports in the literature and unclear clinical significance. We report the incidental finding of unilateral TFL agenesis in a 25-year-old male physician who had been enrolled as a healthy control in a muscle MRI study on genetic myopathies. Imaging demonstrated a complete absence of the right TFL with mild compensatory hypertrophy of the ipsilateral rectus femoris, while the contralateral side and all other muscles appeared normal. The subject had no history of neuromuscular disease, exhibited only a subtle waddling gait, and had previously completed the New York Marathon in 4 h and 16 min without symptoms. Laboratory tests, including creatine kinase, were within normal limits. Thirteen years later, he remains in good health, continues regular sports activities, and has not developed pain or functional impairment. This case emphasizes that TFL agenesis may remain clinically silent and compatible with high levels of physical activity. Nevertheless, awareness of such anomalies is important, as compensatory mechanisms might predispose to long-term biomechanical imbalance, and recognition on imaging can prevent misinterpretation or unnecessary investigations.

偶然发现的单侧阔筋膜张肌发育不全在马拉松运动员:一个未报道的现象。
先天性阔筋膜张肌发育不全是一种极为罕见的畸形,文献报道很少,临床意义不明。我们报告一位25岁的男性医生偶然发现单侧TFL发育不全,他作为健康对照参加了一项关于遗传性肌病的肌肉MRI研究。影像学显示右侧TFL完全缺失,同侧股直肌轻度代偿性肥大,而对侧及所有其他肌肉均正常。受试者无神经肌肉疾病史,仅表现出轻微的摇摇晃晃的步态,之前在4小时16分钟内完成了纽约马拉松比赛,没有任何症状。实验室检查,包括肌酸激酶,都在正常范围内。13年后,他身体健康,继续定期进行体育活动,没有出现疼痛或功能障碍。本病例强调TFL发育可能在临床上保持沉默,并与高水平的体育活动相适应。然而,意识到这种异常是很重要的,因为代偿机制可能会导致长期的生物力学失衡,而在影像学上的识别可以防止误解或不必要的调查。
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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来源期刊
Diagnostics
Diagnostics Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
4.70
自引率
8.30%
发文量
2699
审稿时长
19.64 days
期刊介绍: Diagnostics (ISSN 2075-4418) is an international scholarly open access journal on medical diagnostics. It publishes original research articles, reviews, communications and short notes on the research and development of medical diagnostics. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodological details must be provided for research articles.
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