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马拉松运动员单侧阔筋膜张肌发育不全的偶然发现:一种未报道的现象。

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

作者信息

Bellini Tommaso, Bruno Claudio, Brisca Giacomo

机构信息

Pediatric Emergency Room and Emergency Medicine Unit, Emergency Department, IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy.

Centre of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy.

出版信息

Diagnostics (Basel). 2025 Sep 20;15(18):2396. doi: 10.3390/diagnostics15182396.

DOI:10.3390/diagnostics15182396
PMID:41008767
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12468499/
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.

摘要

阔筋膜张肌先天性发育不全是一种极其罕见的异常情况,文献报道极少,临床意义尚不明确。我们报告了一名25岁男性内科医生单侧阔筋膜张肌发育不全的偶然发现,该医生在一项关于遗传性肌病的肌肉MRI研究中作为健康对照入选。影像学检查显示右侧阔筋膜张肌完全缺如,同侧股直肌有轻度代偿性肥大,而对侧及所有其他肌肉均正常。该患者无神经肌肉疾病史,仅表现出轻微的摇摆步态,此前曾在4小时16分钟内完成纽约马拉松赛且无症状。包括肌酸激酶在内的实验室检查结果均在正常范围内。13年后,他依然健康,继续定期进行体育活动,未出现疼痛或功能障碍。该病例强调阔筋膜张肌发育不全可能在临床上没有症状,且与高水平的体力活动相容。然而,认识到这类异常情况很重要,因为代偿机制可能导致长期的生物力学失衡,而影像学上的识别可以避免误解或不必要的检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d157/12468499/366d39d8d026/diagnostics-15-02396-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d157/12468499/5b58f6480bb7/diagnostics-15-02396-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d157/12468499/366d39d8d026/diagnostics-15-02396-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d157/12468499/5b58f6480bb7/diagnostics-15-02396-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d157/12468499/366d39d8d026/diagnostics-15-02396-g002.jpg

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本文引用的文献

1
Isolated pathologies of Tensor Fasciae Latae: Retrospective cohort analysis from a tertiary referral centre.阔筋膜张肌孤立性病变:来自三级转诊中心的回顾性队列分析。
J Clin Orthop Trauma. 2022 Apr 20;29:101870. doi: 10.1016/j.jcot.2022.101870. eCollection 2022 Jun.
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Femoral head necrosis and progressive osteoarthritis of a healed intracapital osteotomy in a severe sequelae of Legg-Calvé-Perthes disease with aplasia of tensor fasciae latae.股骨头坏死以及已愈合的经股骨颈截骨术的进行性骨关节炎,这是Legg-Calvé-Perthes病的严重后遗症,伴有阔筋膜张肌发育不全。
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人类胚胎和胎儿中的阔筋膜张肌,特别提及它对髂胫束发育的贡献。
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Three different manifestations of congenital muscular aplasia in a family.一个家族中先天性肌肉发育不全的三种不同表现形式。
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