Fodor Marius, Fodor Lucian, Ciuce Constantin
Vascular Surgery Unit, First Surgical Clinic, Emergency District Hospital, University of Medicine and Pharmacy, Cluj Napoca, Romania.
Ann Vasc Surg. 2011 Oct;25(7):961-8. doi: 10.1016/j.avsg.2011.05.019. Epub 2011 Aug 10.
Thoracic outlet syndrome (TOS) identifies the clinical condition determined by the mechanical compression and entrapment of the subclavian vessels and the brachial plexus cords within the space delineated by the scalene muscles, the clavicle, and the first rib. To date, there are no concluding explanations concerning the real causes of the appearance of TOS in children. This is the first study to investigate the existence, frequency, and type of thoracic outlet anomalies in the prenatal stage (human fetuses).
Eighty cervical dissections (40 consecutive spontaneously aborted human fetuses) were performed, and the musculoskeletal, vascular, and nervous elements that pass through the thoraco-cervico-axillary region were investigated.
Overall, anatomical anomalies of the thoraco-cervico-axillary region were found in 60% of the 80 cervical dissections. Nine (22.5%) of the 40 fetuses had normal bilateral anatomy. In 6.3%, the scalene hiatus had an oval shape due to the common costal insertion of the anterior and middle scalene muscles. Fibromuscular bands were found in 15% of the fetuses. Hypertrophy of the anterior scalene muscle was seen in 12.5% of the dissections. In 28.7% of the cervical dissections, hypertrophy of the C7 transversal process was noted, bilateral in seven cases. There was one case of a "C-shaped" clavicle anomaly. The absence of the internal mammary artery was noted in one case.
This study shows that the presence of TOS anomalies in fetuses is not a rare occurrence, emphasizing a pathological cervical background which can be harmful in situations of cervical trauma or inflammatory processes. Having knowledge of the types of anomalies which can lead to TOS is important for performing a complete surgical correction and avoiding the high failure rate of recurrent TOS.
胸廓出口综合征(TOS)指的是由锁骨下血管和臂丛神经束在由斜角肌、锁骨和第一肋骨所界定的空间内受到机械性压迫和卡压所导致的临床病症。迄今为止,关于儿童出现TOS的真正原因尚无定论。这是第一项研究产前阶段(人类胎儿)胸廓出口异常的存在、频率和类型的研究。
进行了80例颈部解剖(40例连续的自然流产人类胎儿),并对穿过胸-颈-腋区域的肌肉骨骼、血管和神经成分进行了研究。
总体而言,在80例颈部解剖中,60%发现了胸-颈-腋区域的解剖异常。40例胎儿中有9例(22.5%)双侧解剖结构正常。6.3%的胎儿因前斜角肌和中斜角肌共同附着于肋骨而使斜角肌裂孔呈椭圆形。15%的胎儿发现有纤维肌性束带。12.5%的解剖中可见前斜角肌肥大。在28.7%的颈部解剖中,发现C7横突肥大,7例为双侧肥大。有1例“C形”锁骨异常。1例发现胸廓内动脉缺如。
本研究表明,胎儿中存在TOS异常并非罕见情况,强调了一种病理性的颈部背景,在颈部创伤或炎症过程中可能有害。了解可导致TOS的异常类型对于进行完整的手术矫正以及避免复发性TOS的高失败率很重要。