MRI findings in thoracic outlet syndrome

Aralasmak A., Cevikol C., KARAALİ K., ŞENOL A. U., SHARIFOV R., Kilicarslan R., ...Daha Fazla

SKELETAL RADIOLOGY, cilt.41, sa.11, ss.1365-1374, 2012 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Derleme
  • Cilt numarası: 41 Sayı: 11
  • Basım Tarihi: 2012
  • Doi Numarası: 10.1007/s00256-012-1485-3
  • Dergi Adı: SKELETAL RADIOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1365-1374
  • Anahtar Kelimeler: Arterial, Venous, Neurogenic thoracic outlet syndrome, Neurovascular syndrome, Brachial plexus, Scalenus anticus syndrome, Costoclavicular syndrome, Congenital bone variations, Congenital fibromuscular anomalies, Positional, SUBCLAVIUS POSTICUS, BRACHIAL-PLEXUS, DIAGNOSIS, MUSCLE
  • Akdeniz Üniversitesi Adresli: Evet

Özet

We discuss MRI findings in patients with thoracic outlet syndrome (TOS). A total of 100 neurovascular bundles were evaluated in the interscalene triangle (IS), costoclavicular (CC), and retropectoralis minor (RPM) spaces. To exclude neurogenic abnormality, MRIs of the cervical spine and brachial plexus (BPL) were obtained in neutral. To exclude compression on neurovascular bundles, sagittal T1W images were obtained vertical to the longitudinal axis of BPL from spinal cord to the medial part of the humerus, in abduction and neutral. To exclude vascular TOS, MR angiography (MRA) and venography (MRV) of the subclavian artery (SA) and vein (SV) in abduction were obtained. If there is compression on the vessels, MRA and MRV of the subclavian vessels were repeated in neutral. Seventy-one neurovascular bundles were found to be abnormal: 16 arterial-venous-neurogenic, 20 neurogenic, 1 arterial, 15 venous, 8 arterial-venous, 3 arterial-neurogenic, and 8 venous-neurogenic TOS. Overall, neurogenic TOS was noted in 69%, venous TOS in 66%, and arterial TOS in 39%. The neurovascular bundle was most commonly compressed in the CC, mostly secondary to position, and very rarely compressed in the RPM. The cause of TOS was congenital bone variations in 36%, congenital fibromuscular anomalies in 11%, and position in 53%. In 5%, there was unilateral brachial plexitis in addition to compression of the neurovascular bundle. Severe cervical spondylosis was noted in 14%, contributing to TOS symptoms. For evaluation of patients with TOS, visualization of the brachial plexus and cervical spine and dynamic evaluation of neurovascular bundles in the cervicothoracobrachial region are mandatory.