Zusätzliches Halsrippen-Syndrom

Cervical rib syndrome, also referred to as Naffziger’s syndrome, represents a constellation of clinical symptoms arising from an exceptionally rare congenital anomaly within the osteomuscular system, affecting approximately 1% of the general population. The primary pathological mechanism involves the development of an aberrant bony structure, colloquially termed a cervical or supernumerary rib. This condition typically results in abnormal compression of neural and vascular structures supplying the upper quadrant of the torso—specifically the upper limb and the cervicothoracic junction of the spine. Consequently, patients experience a significant decline in functional capacity, manifesting as multiple impairments in daily activities. Furthermore, this syndrome frequently coexists with overuse injuries and pathological alterations in the sternocleidomastoid muscle, as well as scapular depression, which may be attributed to age-related degenerative processes or chronic mechanical stress.

Cervical rib syndrome predominantly arises as a consequence of congenital developmental anomalies within the skeletal system, wherein an supernumerary rib-like structure forms. This condition is classified as a distinct variant of a broader pathological spectrum known as thoracic outlet syndrome. The resultant osseous formation may exhibit considerable variability in both size and morphology, with its anatomical localization most frequently involving the C7 vertebral segment. It is not uncommon for the cervical rib to undergo further development, establishing connections with adjacent skeletal components—typically the first pair of ribs—through either rigid (osseous) or more pliable (fibrous) ankylosis. Beyond its congenital etiology, this syndrome may also emerge due to a constellation of predisposing factors, including the prolonged maintenance of improper posture, which precipitates a reduction in cervical lordosis and excessive anterior displacement of the head, ultimately leading to scapular protraction and elevation. Additionally, clinicians identify contributing factors such as mechanical trauma, chronic stress fostering non-ergonomic postural habits, muscular hypertrophy stemming from repetitive motion sequences (e.g., in professional athletes), and surgical interventions, notably sternotomy—a procedure involving the division of the sternum to access the cardiac muscle. It is also noteworthy that this syndrome may develop secondarily in association with factors such as macromastia, breast implants, or prior mastectomy procedures. Clinical manifestations are intrinsically linked to the presence of the osseous protrusion, which exerts compressive forces on neurovascular structures, thereby eliciting characteristic symptomatology, including pain, sensory disturbances, and functional impairments.

To definitively confirm the presence of cervical rib syndrome, a comprehensive imaging-based diagnostic protocol must be implemented to visualize the anomalous bony structure. Primary diagnostic modalities include thoracic and cervical spine radiography, supplemented by ultrasonography employing advanced dual-contrast imaging techniques. In clinically justified cases, the evaluation may be extended to include specialized procedures such as arterial angiography, electrophysiological muscle activity assessment (electromyography), contrast-enhanced venous imaging (phlebography), and non-invasive peripheral vascular flow analysis (rheoangiography). Therapeutic management is exclusively surgical, with the core objective of decompressing the affected neurovascular structures. The procedure involves the precise excision of the cervical rib and—in the majority of clinical scenarios—the first pair of thoracic ribs. A critical prerequisite for surgical planning is a multidisciplinary consultation incorporating cardiac, neurological, and orthopedic assessments to refine the treatment strategy and mitigate potential intraoperative or postoperative complications.