Sprengel deformity, named after Sprengel is as congenital high of the scapula. Sprengel deformity is a congenital anomaly associated with malposition and dysplasia of the scapula causing disfigurement and limitation of shoulder movement.
Sprengel deformity is the most common congenital malformation of the shoulder girdle affecting males three times more than females.
The condition is sporadic but may be found in families in autosomal dominant inheritance.
The condition occurs due to failure of descent of scapula.In embryo, the scapula is a cervical appendage that differentiates opposite the fourth, fifth, and sixth cervical vertebrae at about 5 weeks.
By third month of intrauterine life, in a normal foetus, it comes down to thorax in its usual place.
Development of bone, cartilage, and muscle also occurs resulting in absent or hypoplastic trapezius, rhomboid, or levator scapulae.
Serratus anterior, pectoralis major, latissimus dorsi, or the sternocleidomastoid may also be involved
Changes in Sprengel Deformity
The affected scapula in Sprengel’s deformity is abnormally high. It is small, with a smaller vertical diameter and an apparently greater width. Its shape is distorted, is smaller than normal in the vertical plane and appears larger horizontally.
The inferior angle is rotated medially, causing the glenoid to face inferiorly.
An omovertebral bar is a fibrous, cartilaginous, or bony connection that exists in about one third of cases and spans the superomedial angle of the scapula to the spinous process, lamina, or transverse process of the cervical vertebrae.
It adds to restriction of shoulder motion.
The shoulder girdle musculature is usually defective, the trapezius being most often affected. The muscle may be absent or weak, especially in its lower portion. The rhomboids and levator scapulae are usually hypoplastic and partially fibrosed. The serratus anterior may be weak.
The pectoralis major, pectoralis minor, latissimus dorsi, and sternocleidomastoid muscles may be affected.
Associated Congenital Deformities
- Absence or fusion of ribs
- Cervical ribs
- Klippel-Feil syndrome
- Congenital scoliosis with hemivertebrae
- Spina bifida in the cervical region
- Situs inversus
- Mandibulofacial dysostosis.
The humerus may be shortened on the affected side.
The clavicle may be malformed or hypoplastic, or it may fail to articulate with the acromion. Congenital shortening of the femur, incomplete intercalary tibial hemimelia, radial hemimelia, and ray defects of the hand and foot are other rare associated congenital anomalies.
Kidney malformations, such as ectopia, hypoplasia or absence of a kidney are infrequent but do occur.
Classification of Sprengel Deformity
The classification by Cavendish is based on the severity of the Sprengel deformity [also called Cavendish grades]
Mild deformity. The shoulders are almost level, and the deformity cannot be noticed with the clothes on.
Mild deformity. The shoulders are almost level, but the superomedial portion of the high scapula is visible as a lump.
Moderate deformity. The affected shoulder is elevated 2-5 cm higher than the opposite shoulder.
Severe deformity. The scapula is very high, with the superomedial angle at the occiput, with neck webbing.
The asymmetry of the shoulder caused by the upward and forward displacement of the scapula is the salient physical finding.
The deformity is usually noticed at birth; it progresses with growth. It is more preponderant in girls.
The deformity may be bilateral. The level of the scapula in relation to the vertebral column varies with the severity of the condition.
On the affected side, the neck is fuller and shorter. The affected scapula is often tilted obliquely upward and laterally at an angle of 25 degree from the horizontal.
Passive motion of the glenohumeral joint is usually within normal range. Scapulocostal motion is restricted owing to loss or marked decrease of mobility of the scapula over the thorax secondary to omovertebral bone or fibrous adhesions binding the scapula to the ribs.
When the condition is bilateral, the neck appears very short and thick. Abduction is limited in both shoulders, and the cervical lordosis may be increased.
There are few syndromes in which Sprengel deformity may be associated. These are quite rare syndromes.
- Klippel-Feil syndrome
- Greig syndrome
- Poland syndrome
- VATER (ie, vertebral defects, imperforate anus, tracheoesophageal fistula, and radial and renal dysplasia)
- Velocardiofacial syndrome
- Floating-harbor syndrome
- Goldenhar syndrome
- X-linked dominant hydrocephalus, skeletal anomalies, and mental disturbance syndrome
Radiograms will demonstrate the elevation of the scapula and its associated bony deformities. They are best visualized by taking the following views
- Anteroposterior views of both shoulders with the arms at the sides and with the shoulders in both maximal active and passive abduction
- Lateral view of the cervical and dorsal spine to rule out associated spinal anomalies
- Oblique and lateral views of the scapula to demonstrate the omovertebral bone.
CT scans with 3-D reconstruction may be performed to visualize the pathoanatomy of the affected region and to visualize the omovertebral bar. CT is useful in planning for surgery.
In patients where surgical correction is not required, the treatment consists of physical therapy for providing strength and range of motion. In infants and young children, passive and active stretching should be initiated.
If deformity is severe and functional impairment is high surgical correction mus be considered.
The main objectives in performing surgery are to improve the cosmetic appearance and contour of the neck and to improve the scapular function when it is severely impaired. Best surgical results are obtained before 8 years of age.
Surgery removes the structure that bind the scapula and relocates it.
Modified Green scapuloplasty and Woodward procedures are most successful in Sprengel deformity.
Both are done in moderated to severe cases of the deformity.
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