- Published on
Orthopaedic Surgery - Torticollis
Basics
Torticollis is a condition in which the:
Head and neck are held in an abnormal tilted and rotated position.
The deformity may result from:
Muscular
Skeletal
Neurologic
or other systemic abnormalities.
Typical Posture
The characteristic posture consists of:
Lateral flexion of the head toward one side
with rotation of the:
Chin toward the opposite side.
Classification
Torticollis can broadly be divided into:
Congenital
and
Acquired forms.
Congenital Torticollis
Congenital causes include:
Congenital muscular torticollis
and
Congenital cervical skeletal abnormalities.
Acquired Torticollis
Acquired torticollis may result from:
Trauma
Inflammation
Atlantoaxial rotatory subluxation
Neurologic disease
Ocular disorders
or other:
Systemic conditions.
Synonyms
Historical terms include:
Wry neck
Congenital wry neck
Skeletal wry neck
and
Cock-robin deformity.
Sandifer Syndrome
Sandifer syndrome refers to episodic torticollis or abnormal head positioning associated with:
Gastroesophageal reflux
and sometimes:
Hiatal hernia.
Prevention
Prompt recognition and treatment of the underlying cause may prevent:
Fixed deformity
and reduce the need for:
Surgery.
Epidemiology
Torticollis can occur at:
Any age
depending on the underlying cause.
Congenital Muscular Torticollis
Congenital muscular torticollis usually becomes apparent during the first:
6–8 weeks of life.
Atlantoaxial Rotatory Subluxation
In children, one important acquired cause is:
Atlantoaxial rotatory subluxation.
This may follow:
Upper respiratory infection
Pharyngitis
or
Trauma.
Sex
Males and females are affected approximately:
Equally.
Incidence
Because torticollis has many causes, the exact incidence is difficult to define.
Historical estimates range from approximately:
1 in 100
to
1 in 1,000 individuals.
Risk Factors
Risk factors depend on the specific:
Etiology.
Congenital Muscular Torticollis Risk Factors
Potential associations include:
Difficult delivery
Birth trauma
and localized injury or ischemia involving the:
Sternocleidomastoid muscle.
Atlantoaxial Rotatory Subluxation Risk Factors
Potential triggers include:
Upper respiratory infection
Pharyngitis
and
Neck trauma.
Genetics
Several congenital disorders associated with torticollis have:
Genetic components.
Down Syndrome
Down syndrome is an important genetic condition associated with:
Cervical instability
including abnormalities involving the:
Atlantoaxial joint.
Etiology
The cause depends on whether the disorder is:
Muscular
Skeletal
Neurologic
Inflammatory
or
Traumatic.
Congenital Muscular Torticollis
Congenital muscular torticollis results from shortening and fibrosis of the:
Sternocleidomastoid muscle.
Sternocleidomastoid Effect
Contracture of one sternocleidomastoid causes the head to:
Tilt toward the affected side
while the chin rotates:
Away from the affected side.
Congenital Bony Torticollis
Congenital skeletal causes include abnormalities of the:
Occipitocervical junction
and
Cervical vertebrae.
Bony Abnormalities
Examples include:
Cervical hemivertebrae
Congenital vertebral fusion
and
Asymmetry of the occipital condyles.
Atlantoaxial Rotatory Subluxation
This condition involves abnormal rotation of:
C1 relative to C2.
It may occur after:
Trauma
Inflammation
or occasionally as part of a:
Congenital abnormality.
Diagnosis
Diagnosis begins with careful assessment of:
Head position
Neck motion
Neurologic status
and possible:
Underlying systemic disease.
Signs and Symptoms
The hallmark feature is:
Head tilt with restricted cervical range of motion.
Direction of Motion
The patient may be able to rotate the head farther:
Away from the neutral position
but may have difficulty rotating toward:
Correction.
Neck Mass
Infants with congenital muscular torticollis may have a palpable:
Sternocleidomastoid mass.
This represents localized:
Fibrosis or thickening.
Pain
Pain is less prominent in infants but is more common in:
Older children and adults.
Occipital Symptoms
Some patients report:
Occipital pain
Vertigo
or
Dizziness
that worsens with certain:
Head movements.
Plagiocephaly
Persistent torticollis in infancy may cause secondary:
Plagiocephaly
or facial:
Asymmetry.
Physical Examination
Observe the patient’s:
Head
Face
Neck
and
Shoulder alignment.
Characteristic Position
The ear is typically tilted toward the:
Affected side
while the chin points toward the:
Opposite side.
Range of Motion
Assess:
Active
and
Passive cervical rotation
and
Lateral flexion.
Sternocleidomastoid Examination
Palpate the sternocleidomastoid for:
Tightness
Fibrosis
or a localized:
Mass.
Craniofacial Asymmetry
Longstanding torticollis may produce:
Flattening of the skull
Facial asymmetry
or altered:
Ear position.
Cervical Skeletal Abnormality
A patient with congenital cervical fusion may have a:
Short neck
Low posterior hairline
and reduced:
Cervical motion.
These findings may suggest:
Klippel-Feil syndrome.
Neurologic Examination
A complete neurologic examination should assess:
Strength
Sensation
Reflexes
and
Coordination.
Laboratory Tests
There are no laboratory tests specific for:
Torticollis.
Inflammatory or Neoplastic Evaluation
If infection, inflammatory disease, or malignancy is suspected, laboratory studies may include:
CBC
ESR
and
C-reactive protein.
Additional Specialist Evaluation
When no obvious musculoskeletal cause is present, additional assessment may be needed by:
Ophthalmology
Audiology
or
Gastroenterology.
Imaging
Plain Radiographs
AP and lateral cervical spine radiographs may be used to identify:
Congenital bony abnormalities
Fracture
Dislocation
or abnormal:
Alignment.
CT
CT is particularly useful for evaluating:
Atlantoaxial rotatory subluxation
Occipitocervical injury
Fracture
or
Dislocation.
Rotatory Subluxation
CT may demonstrate persistent abnormal rotational alignment between:
C1
and
C2.
MRI
MRI is indicated when there is concern for:
Spinal cord
Brainstem
Soft-tissue
or other:
Neurologic lesions.
Pathological Findings
In congenital muscular torticollis, the:
Sternocleidomastoid muscle
typically demonstrates:
Fibrosis
and
Shortening.
Differential Diagnosis
The differential diagnosis is broad.
Neurogenic Causes
Potential neurologic causes include:
Brainstem tumor
Cervical spinal cord tumor
Cerebellar tumor
and
Syringomyelia.
Ocular Causes
An ocular disorder may cause compensatory:
Head tilt
to optimize:
Vision.
Traumatic Causes
Traumatic causes include:
Atlantoaxial subluxation
Cervical fracture
and
Occipitocervical dislocation.
Inflammatory Causes
Potential causes include:
Cervical lymphadenitis
and
Rheumatoid arthritis.
Congenital Skeletal Causes
Examples include:
Hemivertebra
Congenital fusion
and
Occipital condyle asymmetry.
Gastrointestinal Cause
In infants, episodic abnormal head positioning may result from:
Sandifer syndrome
associated with:
Gastroesophageal reflux.
Treatment
Treatment depends on the:
Underlying cause
and duration of the:
Deformity.
Congenital Muscular Torticollis
Early treatment consists primarily of:
Stretching exercises.
Early Prognosis
When treatment begins before approximately:
1 year of age
stretching is successful in the vast majority of:
Infants.
Positioning
Parents can position:
Toys
Lights
or other points of interest so the child is encouraged to rotate the head toward the:
Restricted side.
Home Program
A structured home stretching program should focus on:
Gentle cervical rotation
and
Lateral flexion.
Atlantoaxial Rotatory Subluxation
Recent-onset atlantoaxial rotatory subluxation may respond to:
Rest
Analgesics
Physical therapy
and a:
Soft cervical collar.
Early Treatment
Patients treated within approximately the:
First week
often recover without:
Surgery.
Muscle Relaxants
Selected patients may require:
Muscle relaxants
when painful spasm prevents:
Reduction.
Rigid Immobilization
Persistent symptoms may require a:
Hard collar
or another form of:
Cervical bracing.
Traction
If treatment is delayed or the deformity becomes fixed, reduction may require:
Cervical traction.
Activity
Contact sports and strenuous activity should be restricted until the:
Cause is identified
and cervical stability is:
Confirmed.
Physical Therapy
Physical therapy can be curative for many cases of:
Congenital muscular torticollis
and
Recent-onset atlantoaxial rotatory subluxation.
Stretch Direction
The therapist should receive clear instructions regarding:
Direction of stretching
and whether:
Traction
is appropriate.
Medication
Pain may be treated with:
Acetaminophen
or
Ibuprofen
when medically appropriate.
Surgery
Surgery is reserved for selected cases that fail appropriate:
Nonoperative treatment.
Muscular Torticollis Surgery
Persistent congenital muscular torticollis may require:
Sternocleidomastoid release
or
Lengthening.
Timing
Surgery is generally considered when:
Persistent contracture
Restricted motion
or progressive:
Craniofacial asymmetry
remains despite adequate:
Stretching.
Atlantoaxial Rotatory Subluxation Surgery
Severe or chronic atlantoaxial rotatory subluxation that cannot be reduced with:
Traction
may require:
Reduction and C1–C2 fusion.
Congenital Bony Abnormality
Selected congenital cervical abnormalities causing severe persistent deformity or instability may also require:
Spinal fusion.
Follow-Up
Follow-up should assess:
Head position
Range of motion
Neurologic findings
and development of:
Craniofacial asymmetry.
Prognosis
Most cases of torticollis improve:
Spontaneously
or with appropriate:
Treatment.
Early Muscular Torticollis
Congenital muscular torticollis treated early generally has an:
Excellent prognosis.
Delayed Treatment
Delayed treatment increases the risk of:
Persistent contracture
and
Plagiocephaly.
Complications
Potential complications include:
Fixed atlantoaxial subluxation
Persistent neck deformity
and
Plagiocephaly.
Fixed Subluxation
Untreated atlantoaxial rotatory subluxation may become:
Fixed
and increasingly difficult to:
Reduce.
Plagiocephaly
Persistent head positioning in infancy may cause permanent:
Cranial or facial asymmetry
if treatment is delayed beyond the period of active:
Remodeling.
Patient Monitoring
Neurologic status should be followed:
Closely.
Imaging Follow-Up
Bony abnormalities such as persistent:
Atlantoaxial rotatory subluxation
may require repeat:
Imaging.
CT use should be balanced against cumulative:
Radiation exposure, particularly in children.
Clinical Summary
Typical presentation: Head tilted toward one side with the chin rotated to the opposite side and restricted neck motion.
Most common infant cause: Congenital muscular torticollis from sternocleidomastoid fibrosis or contracture.
Important acquired cause in children: Atlantoaxial rotatory subluxation, often after trauma or an upper respiratory infection.
Key examination: Assess cervical ROM, palpate the sternocleidomastoid, look for plagiocephaly, and perform a complete neurologic examination.
Imaging: Plain cervical radiographs for bony abnormalities; CT for suspected C1–C2 rotatory subluxation or fracture; MRI for suspected spinal cord, brainstem, or other neurologic disease.
Initial treatment: Early muscular torticollis responds to stretching and positioning; recent atlantoaxial rotatory subluxation may respond to analgesics, therapy, and cervical immobilization.
Surgery: Reserved for persistent muscular contracture or irreducible/fixed atlantoaxial abnormalities.
Red flags: New neurologic deficits, severe pain, trauma, fever, progressive deformity, or acquired torticollis without an obvious benign explanation.
Key Principle
Torticollis is a clinical posture characterized by lateral head tilt with rotation of the chin in the opposite direction.
It may arise from:
Muscular, skeletal, neurologic, inflammatory, traumatic, ocular, or gastrointestinal causes.
In infants, the most common form is:
Congenital muscular torticollis, which usually responds well to early:
Stretching and positioning.
In older children with acute painful torticollis, especially after:
Trauma or upper respiratory infection, consider:
Atlantoaxial rotatory subluxation.
Persistent, painful, neurologically abnormal, or atypical torticollis requires evaluation for an underlying:
Structural or neurologic cause.