- Case report
- Open Access
Compression of the lower trunk of the brachial plexus by a cervical rib in two adolescent girls: case reports and surgical treatment
© Dahlin et al. 2009
- Received: 26 June 2009
- Accepted: 6 September 2009
- Published: 6 September 2009
Presence of a cervical rib in children is extremely rare, particularly when symptoms of compression of the lower trunk of the brachial plexus occur. We present two cases with such a condition, where two young girls, 11 and 16 years of age were treated by resection of the cervical rib after a supraclavicular exploration of the lower trunk of the brachial plexus. The procedure led to successful results, objectively verified with tests in a work simulator, at one year follow-up.
A cervical rib, articulating into the first rib is typically an asymptomatic condition that is even discovered incidentally. Clinical symptoms from the lower trunk of the brachial plexus by the cervical rib are less frequent. In a pediatric population, a cervical rib with neurogenic symptoms is an extremely rare condition with only single cases treated and reported [1–3]. In the published case reports, resection of the first rib and the attached cervical rib has been done through an axillary or a supraclavicular approach with successful postoperative result at one month after surgery, but long-term results are not available. We present two cases with compression of the lower trunk of the brachial plexus by a cervical rib in two young girls, 11 and 16 years old. The condition was successfully treated by resection of the cervical rib through a supraclavicular approach. At one year follow-up, both patients remained free of recurrent symptoms.
At regular follow-up at 1, 3, 6 and 12 months, she had no remaining symptoms from the lower trunk of the brachial plexus, except a slight allodynia around the scar during the first six months. She had no symptoms during full abduction. Cold intolerance was markedly reduced (none or insignificant) and a Froment's sign was not found. At one year follow-up, she had full range of motion and no impairment of strength compared to the contralateral side. Endurance, isometric and dynamic grip strength showed 9-18% higher values than on the left side. The girl was pleased with the surgical procedure. She continued her leisure activities in gymnastics.
At one year follow-up she had no symptoms in the hand. The preoperative symptoms had disappeared although she still experienced a feeling of impaired strength in the left arm. She had full range of motion and it was not possible to provoke any paraesthesia. Tests of fine motor activity in the hand (Crawford pins and sleeve and Minnesota picking test) showed improved values. Tests in the work simulator showed improvement [isometric test 5% weakness (preoperatively 32%), endurance 54% weaker (preoperatively 62%), isometric test of extension with elevated arm 4% weaker than the right side (preoperatively 16%), endurance of flexion/extension with elevated arm similar value on the right side (preoperative 54% weaker)]. MRI follow-up 11 months after surgery revealed no occurrence of the resected cervical rib. There were no differences compared to the two CT-scans done at three and six months after surgery (done for other reasons; fever investigation and a fall from a horse). The patient was pleased with the surgery. She continued with her previous studies and leisure activities without restriction.
Our patients had cervical ribs bilaterally, but mainly experienced unilateral symptoms, where resection of only the symptomatic cervical rib through a supraclavicular approach was successfully done in both cases. Both girls had symptoms and a history, including pain at night time with a clear suspicion that the lower trunk of the brachial plexus was affected since carrying heavy things and lifting the arm above the shoulder and other activities elicited paraesthesia and numbness particularly in the ulnar part of the hand. Objectively, the impaired function in the arm and the hand was clearly demonstrated with the various tests using a work simulator, indicating the usefulness of such novel investigation pre- and postoperatively in patients with compression of the brachial plexus. The symptoms of the patients corresponded to the findings in the clinical examination and the MRI, indicating the value of MRI. Preoperatively, neurography and EMG did not reveal any specific impairment of nerve function, except an increased F-wave in Case One. However, MRI showed a clear affection of the brachial plexus from the cervical rib in both cases when imaging was done with the arm abducted. This indicates that MRI should be done in the positions that elicit symptoms. The MRI findings were verified when the lower trunk of the brachial plexus was explored. In both cases the nerve structures were riding over the cervical rib with fibrous bands approaching the lower trunk.
Compression of one or more of the neurovascular structures traversing the superior aperture of the chest is generally referred as thoracic outlet syndrome (TOS). This syndrome has been the focus in a large number of articles including description of neurophysiologic examinations, surgical techniques and results, see for example [4–14]. But only a few papers have focused on children and adolescents , and on the importance of cervical rib for irritation of the brachial plexus and the subclavian artery . A thorough history should be taken and appropriate investigations should be undertaken in patients with a suspected TOS to define the cause of symptom and exclude other diagnoses .
In contrast to a previous report , our patients did not have any muscular wasting, but only sensory symptoms, probably explaining the lack of electrophysiological alterations. In both cases, there was a successful relief of symptoms with a complete recovery in the younger girl and with just minor remaining intermittent symptoms in the older girl, at the one-year follow- up. In addition, the preoperative tests performed at our hand rehabilitation unit demonstrated a clear improvement of the results at the regular follow-up at 3, 6 and 12 months. In addition, we could objectively demonstrate improvement by examination of various tasks using the work simulator, indicating its usefulness in pre- and postoperative investigations, which has not been previously utilised. Electrophysiological criteria for neurogenic thoracic outlet syndrome have previously been suggested, such as low amplitude of the median compound muscle action potentials, low or relatively low ulnar sensory nerve action potentials, relatively low amplitude or normal ulnar compound muscle action potential and normal-amplitude median sensory nerve action potential . We found that the electrophysiological investigation showed no abnormalities, which maybe due to the fact that the lower trunk was affected to a limited extent in contrast to other published cases . Electrodiagnostic procedures have previously been discussed in the literature [4, 9, 12]. The brachial plexus in Case Two had a distorted (rotated; a horizontal rather than a vertical plane) direction caused by the cervical rib and the bony formation. We could not observe any signs that the subclavian artery was compressed between the rib and the fibrous bands even if it has been reported that a cervical rib of more than 5.5 cm long tends to lift up and kink the subclavian artery .
We decided to explore the lower trunk through a supraclavicular approach to be able to explore the impact of the cervical rib on the lower trunk due to the disturbing, mainly sensory, symptoms in the patients. Advantages of a supraclavicular exploration for thoracic outlet syndrome have been presented earlier with few reported complications after such approach as compared to a transaxillary resection of the first rib [9, 17, 18], but conflicting opinions exist about the best approach . The presence of a cervical rib and fibrous band form a barrier over which particularly the lower trunk of the brachial plexus enters the arm with a potential microtrauma to the trunk by stretching and compression [19, 20]. Interestingly, even if our present cases had similar cervical ribs bilaterally (just a short one on the right side in the older girl), symptoms only occurred on one side. In the contralateral side of the younger girl the symptoms were extremely rare and therefore no indication for exploration. In the older girl, symptoms occurred on the side where the cervical rib was more prominent; thus, only a rudimentary cervical rib was presented on the asymptomatic side.
We suggest that the presence of a cervical rib even in children may induce true nerve compression, where the symptoms vary with position of the arm causing mainly sensory symptoms in the distribution of the lower trunk. These patients should be carefully examined and investigated, including MRI and various tests in work simulator. The possibility of surgical exploration with resection of the cervical rib should be considered in appropriate cases. We advocate a supraclavicular approach with a careful exploration of the lower trunk and resection of the cervical rib, the bony formation from the first rib and fibrous bands.
Informed consent was obtained from the patients and their parents for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
The research on nerve injury and repair done by the authors are supported by grants from the Swedish Research Council (Medicine), Region Skåne and Funds from the University Hospital Malmö, Sweden. We thank Marianne Neving and Pernilla Vikström at department of Hand Surgery for help with pre- and postoperative examinations at the Hand Rehabilitation unit.
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