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先天性双侧胫骨前肌发育不全:一例罕见病例报告

Congenital bilateral agenesis of the tibialis anterior muscles: a rare case report.

作者信息

Htwe Ohnmar, Swarhib M, Pei Tan Sook, Naicker Amaramalar Selvi, Das S

机构信息

Rehabilitation Unit, Department of Orthopedic and Traumatology, Universiti Kebangsaan Malaysia Medical Centre, Jalan Yaacob Latif, Bandar Tun Razak, Cheras, Kuala Lumpur, Malaysia.

出版信息

Rom J Morphol Embryol. 2012;53(3):657-9.

Abstract

Congenital bilateral agenesis of the tibialis anterior muscles is a rare condition. We present a case of congenital absence of bilateral tibialis anterior muscles in a 6-year-old boy who presented with an abnormal gait. He was previously diagnosed to have bilateral congenital talipes equinovarus (CTEV) deformity for which he underwent corrective surgery two times. However, he still had a residual foot problem and claimed to have difficulty in walking. On examination, he walked with a high stepping gait and muscle power of both lower limbs was 5/5 on the medical research council scale (MRCS) except for both ankle dorsiflexors and long toe extensors. The sensation was intact. Magnetic Resonance Imaging (MRI) study of both legs revealed that tibialis anterior muscles were not visualized on both sides suggestive of agenesis of the tibialis anterior muscles. The rest of the muscles appeared mildly atrophied. The electrophysiological study showed normal motor and sensory conduction in both upper and lower limbs. Electromyographic (EMG) study of the vastus medialis was within normal limit and no response could be elicited for EMG of tibialis anterior muscles suggesting possible absence of tibialis anterior muscles, bilaterally. The patient underwent split tibialis posterior tendon transfer to achieve a balanced and functional foot and was well on discharge. The present case describes the normal anatomy and embryology of tibialis anterior muscles as well as possible causes of its agenesis along with its clinical implications.

摘要

先天性双侧胫前肌发育不全是一种罕见的病症。我们报告一例6岁男孩先天性双侧胫前肌缺如的病例,该男孩表现为异常步态。他之前被诊断为双侧先天性马蹄内翻足(CTEV)畸形,并接受了两次矫正手术。然而,他仍存在残留的足部问题,且自称行走困难。检查时,他以高抬腿步态行走,除双侧踝背屈肌和长趾伸肌外,双下肢肌肉力量根据医学研究委员会(MRC)量表评估为5/5。感觉功能正常。双腿的磁共振成像(MRI)研究显示双侧均未显示出胫前肌,提示胫前肌发育不全。其余肌肉出现轻度萎缩。电生理研究显示上下肢运动和感觉传导正常。股内侧肌的肌电图(EMG)研究在正常范围内,而胫前肌的EMG未引出反应,提示双侧胫前肌可能缺如。该患者接受了胫后肌腱劈开转移术以实现足部的平衡和功能,出院时情况良好。本病例描述了胫前肌的正常解剖结构和胚胎学,以及其发育不全的可能原因及其临床意义。

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