FRCS Paediatric Ortho — improved notes
FRCS Paediatric Ortho — visual inline notes

082. Torticollis

visual-inline rebuild2 extracted figuresspeaker notes XML79 study lines8 Q&A

Individual slide images have been cropped from the rendered slide and inserted beside the matching note section. The full slide remains below only for layout/audit.

Clean FRCS notes with inline figures

•This is a clinical photo showing a paed patient with right sided torticollis
•Evidenced by the head tilting to the right side and rotating to the left side
•There is no plagiocephaly or facial asymmetry noted, over the neck there is no scar, no obvious strabismus noted
•Cock robin posture

History

•Perinatal history (Breech, 1st born, oligohydramios), known congenital conditions (e.g. Klippel Feil syndrome)
•PAIN

Acute painful vs chronic painless

•Onset of symptoms, progression, trauma, previous treatment or H&N
•Any hearing or optical impairment
•Any recently URI sx
•Functional impairment

Examination

Clinical photograph
Fig 1. Clinical photographtop left
Clinical photograph
Fig 2. Clinical photographtop centre
•1. Plagiocephaly, low hair line, scapula (KF syndrome)
•2. Facial dysmorphic features or facial asymmetry
•3. SCM spasm, tumour, cervical LN
•4. Rotation and tilt lag 15deg
•5. Squint, hearing
•6. Neuro exam
•If newborn, look for other packaging disorders

Investigations

•Bloods: CBC, inflammatory markers
•Xray look for lateral mass asymmetry in open mouth view, lateral to see ADI, trapezoidal anterior C1 shadow, oval posterior arch sign. Also to exclude fracture or congenital abnormalities
•Dynamic CT is gold standard for AARI (only book it if failed initial conservative management)
•Look for fixed rotation of C1/2 relationship
•+/- contrast to r/o retropharyngeal abscess if raised inflammatory markers
•+/- MRI to exclude underlying infection or tumor

Fielding CT classification:

•Unilateral subluxation with intact transverse ligament (dens is the pivot point)
•Unilateral ant subluxation 3-5mm (opposite facet acts as pivot)
•Bilateral ant subluxation >5mm
•Post subluxation (dens deficiency)
•Dynamic CT (3 sets) to look for fixed relationship between C1 and C2
•Normal C1/2 rotation
•Phase 1-3
Type / groupDefinition / note
1Purely C1 rotate, up to 21deg (SCM pulls skull, OC segment no rotation)
2C1 C2 rotate together, (C2 pulled by alar ligament)
3C1 C2 fixed and rotate together
•Mx depends on timing
•<1w: Soft neck collar, analgesics
•1-4w: (“1hr off ,3hr on” cycle) 2-3kg till reduced with reverse Trendelenburg (full rotation over both direction) then SOMI 4wk (if failed after 4w to OT)
•>4w: Halo traction 4w as well, high chance of failure then OT x fuse C1/2 (other indications: irreducible >3 months, neurological deficit, recurrent)
•Grisel’s syndrome: drainage of inflammatory mediators through pharyngovertebral vein to periodontoid plexus → ligamentous laxity

•CMT
•Remember to look for other packaging disorders
•Pathophysiology: local compartment syndrome of SCM avascular fibrous band formation
•Operation
•Presentation >1yo
•>15 deg Head tilt, lag, with tumour

Failed conservative management x 6m

•Unipolar (sternal head <3, sternal + clavicular head 3-10)
•Bipolar in > 10 year
•(alternative is Z plasty)
•Bipolar release in a nutshell
•2cm incision below mastoid, strip attachment from bone
•2cm incision above the sterno-clavicular jx, incise platysma, then cut both heads of SCM together w/ the deep fasica;

Postop:

•Intensive stretching for 3 months
•>2yo → add adjustable torticollis brace for 3 months

Dangers in bipolar release?

•Surface – greater auricular nerve
•Underneath – CNXI
•Anterior - facial nerve

Evidence on CMT:

•Cheng 2001 JBJS
•800 patients < 1yo onset
•95% good response to physiotherapy (address flexion, rotation, tilting), mean FU 4.5 yr
•Poor prognostic factors: >15deg rotation deficit, SCM tumor, late presentation (present >1yo)

Torticollis causes:

Congenital: (usually painless):

•CMT, Klippel Feil

Acquired:

•Osseous – AARI (trauma, tumor, infection, odontoid hypoplasia in Down’s and Achondroplasia, JRA/RA) (usually painful)
•Non Osseous – ENT, eye (Squint), CNS (Arnold chiari), Postural (usually painless), neck burns

Child more likely to have AADI:

•Capsular laxity due to hormonal cause
•Facet more transverse

Direct Q&A

Q1 What history should be elicited for Torticollis?
•Perinatal history (Breech, 1st born, oligohydramios), known congenital conditions (e.g. Klippel Feil syndrome)
•PAIN
Q2 What is the acute management for Torticollis?

Onset of symptoms, progression, trauma, previous treatment or H&N

•Any hearing or optical impairment
•Any recently URI sx
•Functional impairment
Q3 What examination findings should be assessed in Torticollis?
•1. Plagiocephaly, low hair line, scapula (KF syndrome)
•2. Facial dysmorphic features or facial asymmetry
•3. SCM spasm, tumour, cervical LN
•4. Rotation and tilt lag 15deg
•5. Squint, hearing
•6. Neuro exam
•If newborn, look for other packaging disorders
Q4 What investigations are listed for Torticollis?

Bloods: CBC, inflammatory markers

•Xray look for lateral mass asymmetry in open mouth view, lateral to see ADI, trapezoidal anterior C1 shadow, oval posterior arch sign. Also to exclude fracture or congenital abnormalities
•Dynamic CT is gold standard for AARI (only book it if failed initial conservative management)
•Look for fixed rotation of C1/2 relationship
•+/- contrast to r/o retropharyngeal abscess if raised inflammatory markers
•+/- MRI to exclude underlying infection or tumor
Q5 How is Torticollis classified here?
•Unilateral subluxation with intact transverse ligament (dens is the pivot point)
•Unilateral ant subluxation 3-5mm (opposite facet acts as pivot)
•Bilateral ant subluxation >5mm
•Post subluxation (dens deficiency)
•Dynamic CT (3 sets) to look for fixed relationship between C1 and C2
•Normal C1/2 rotation
•Phase 1-3
•1: Purely C1 rotate, up to 21deg (SCM pulls skull, OC segment no rotation)
•2: C1 C2 rotate together, (C2 pulled by alar ligament)
•3: C1 C2 fixed and rotate together

Mx depends on timing

•<1w: Soft neck collar, analgesics
•1-4w: (“1hr off ,3hr on” cycle) 2-3kg till reduced with reverse Trendelenburg (full rotation over both direction) then SOMI 4wk (if failed after 4w to OT)
•>4w: Halo traction 4w as well, high chance of failure then OT x fuse C1/2 (other indications: irreducible >3 months, neurological deficit, recurrent)
•Grisel’s syndrome: drainage of inflammatory mediators through pharyngovertebral vein to periodontoid plexus → ligamentous laxity
Q6 What thresholds, cut-offs, or criteria are listed under Failed conservative management x 6m?
•Unipolar (sternal head <3, sternal + clavicular head 3-10)
•Bipolar in > 10 year
•(alternative is Z plasty)
•Bipolar release in a nutshell
•2cm incision below mastoid, strip attachment from bone
•2cm incision above the sterno-clavicular jx, incise platysma, then cut both heads of SCM together w/ the deep fasica;
Q7 Dangers in bipolar release?

Surface – greater auricular nerve

•Underneath – CNXI
•Anterior - facial nerve
Q8 What evidence or study finding is cited for Torticollis?

Cheng 2001 JBJS

•800 patients < 1yo onset
•95% good response to physiotherapy (address flexion, rotation, tilting), mean FU 4.5 yr
•Poor prognostic factors: >15deg rotation deficit, SCM tumor, late presentation (present >1yo)

Raw speaker-note hierarchy audit

#lvlmarLindentlogicaloriginal note line
10NoneNone0This is a clinical photo showing a paed patient with right sided torticollis
20NoneNone0Evidenced by the head tilting to the right side and rotating to the left side
30NoneNone0There is no plagiocephaly or facial asymmetry noted, over the neck there is no scar, no obvious strabismus noted
40NoneNone0Cock robin posture
50NoneNone0Hx
60NoneNone0Perinatal history (Breech, 1st born, oligohydramios), known congenital conditions (e.g. Klippel Feil syndrome)
70NoneNone0PAIN
80NoneNone0Acute painful vs chronic painless
90NoneNone0Onset of symptoms, progression, trauma, previous treatment or H&N
100NoneNone0Any hearing or optical impairment
110000Any recently URI sx
120000Functional impairment
130NoneNone0PE
140NoneNone01. Plagiocephaly, low hair line, scapula (KF syndrome)
1500002. Facial dysmorphic features or facial asymmetry
160NoneNone03. SCM spasm, tumour, cervical LN
170NoneNone04. Rotation and tilt lag 15deg
180NoneNone05. Squint, hearing
190NoneNone06. Neuro exam
200NoneNone0If newborn, look for other packaging disorders
210NoneNone0Ix:
220NoneNone0Bloods: CBC, inflammatory markers
230000Xray look for lateral mass asymmetry in open mouth view, lateral to see ADI, trapezoidal anterior C1 shadow, oval posterior arch sign. Also to exclude fracture or congenital abnormalities
240000Dynamic CT is gold standard for AARI (only book it if failed initial conservative management)
250000Look for fixed rotation of C1/2 relationship
260000+/- contrast to r/o retropharyngeal abscess if raised inflammatory markers
270000+/- MRI to exclude underlying infection or tumor
280000Fielding CT classification:
291685800-2286002Unilateral subluxation with intact transverse ligament (dens is the pivot point)
301685800-2286002Unilateral ant subluxation 3-5mm (opposite facet acts as pivot)
311685800-2286002Bilateral ant subluxation >5mm
321685800-2286002Post subluxation (dens deficiency)
330000Dynamic CT (3 sets) to look for fixed relationship between C1 and C2
340000Normal C1/2 rotation
350000Phase 1-3
361457200011: Purely C1 rotate, up to 21deg (SCM pulls skull, OC segment no rotation)
371457200012: C1 C2 rotate together, (C2 pulled by alar ligament)
381457200013: C1 C2 fixed and rotate together
390000Mx depends on timing
400000<1w: Soft neck collar, analgesics
4100001-4w: (“1hr off ,3hr on” cycle) 2-3kg till reduced with reverse Trendelenburg (full rotation over both direction) then SOMI 4wk (if failed after 4w to OT)
421001>4w: Halo traction 4w as well, high chance of failure then OT x fuse C1/2 (other indications: irreducible >3 months, neurological deficit, recurrent)
430000Grisel’s syndrome: drainage of inflammatory mediators through pharyngovertebral vein to periodontoid plexus → ligamentous laxity
440000===================================
450NoneNone0CMT
460NoneNone0Remember to look for other packaging disorders
470NoneNone0Pathophysiology: local compartment syndrome of SCM avascular fibrous band formation
480NoneNone0OT:
490171450-1714501Presentation >1yo
500171450-1714501>15 deg Head tilt, lag, with tumour
510171450-1714501Failed conservative management x 6m
520000Unipolar (sternal head <3, sternal + clavicular head 3-10)
530000Bipolar in > 10 year
540000(alternative is Z plasty)
550NoneNone0Bipolar release in a nutshell
560NoneNone02cm incision below mastoid, strip attachment from bone
570NoneNone02cm incision above the sterno-clavicular jx, incise platysma, then cut both heads of SCM together w/ the deep fasica;
580000Postop:
590000Intensive stretching for 3 months
600000>2yo → add adjustable torticollis brace for 3 months
610000Dangers in bipolar release?
620171450-1714501Surface – greater auricular nerve
630171450-1714501Underneath – CNXI
640171450-1714501Anterior - facial nerve
650000Evidence on CMT:
660000Cheng 2001 JBJS
670000800 patients < 1yo onset
68000095% good response to physiotherapy (address flexion, rotation, tilting), mean FU 4.5 yr
690000Poor prognostic factors: >15deg rotation deficit, SCM tumor, late presentation (present >1yo)
700000===================================
710NoneNone0Torticollis causes:
720NoneNone0Congenital: (usually painless):
730171450-1714501CMT, Klippel Feil
740NoneNone0Acquired:
750171450-1714501Osseous – AARI (trauma, tumor, infection, odontoid hypoplasia in Down’s and Achondroplasia, JRA/RA) (usually painful)
760171450-1714501Non Osseous – ENT, eye (Squint), CNS (Arnold chiari), Postural (usually painless), neck burns
770000Child more likely to have AADI:
780000Capsular laxity due to hormonal cause
790000Facet more transverse

Improved semantic hierarchy used for the study notes

#semantic levelsection?rewritten line
10This is a clinical photo showing a paed patient with right sided torticollis
21Evidenced by the head tilting to the right side and rotating to the left side
31There is no plagiocephaly or facial asymmetry noted, over the neck there is no scar, no obvious strabismus noted
41Cock robin posture
50yesHistory
61Perinatal history (Breech, 1st born, oligohydramios), known congenital conditions (e.g. Klippel Feil syndrome)
71PAIN
80yesAcute painful vs chronic painless
91Onset of symptoms, progression, trauma, previous treatment or H&N
101Any hearing or optical impairment
111Any recently URI sx
121Functional impairment
130yesExamination
1411. Plagiocephaly, low hair line, scapula (KF syndrome)
1512. Facial dysmorphic features or facial asymmetry
1613. SCM spasm, tumour, cervical LN
1714. Rotation and tilt lag 15deg
1815. Squint, hearing
1916. Neuro exam
201If newborn, look for other packaging disorders
210yesInvestigations
221Bloods: CBC, inflammatory markers
231Xray look for lateral mass asymmetry in open mouth view, lateral to see ADI, trapezoidal anterior C1 shadow, oval posterior arch sign. Also to exclude fracture or congenital abnormalities
241Dynamic CT is gold standard for AARI (only book it if failed initial conservative management)
251Look for fixed rotation of C1/2 relationship
261+/- contrast to r/o retropharyngeal abscess if raised inflammatory markers
271+/- MRI to exclude underlying infection or tumor
280yesFielding CT classification:
292Unilateral subluxation with intact transverse ligament (dens is the pivot point)
302Unilateral ant subluxation 3-5mm (opposite facet acts as pivot)
312Bilateral ant subluxation >5mm
322Post subluxation (dens deficiency)
331Dynamic CT (3 sets) to look for fixed relationship between C1 and C2
341Normal C1/2 rotation
351Phase 1-3
3611: Purely C1 rotate, up to 21deg (SCM pulls skull, OC segment no rotation)
3712: C1 C2 rotate together, (C2 pulled by alar ligament)
3813: C1 C2 fixed and rotate together
391Mx depends on timing
401<1w: Soft neck collar, analgesics
4111-4w: (“1hr off ,3hr on” cycle) 2-3kg till reduced with reverse Trendelenburg (full rotation over both direction) then SOMI 4wk (if failed after 4w to OT)
421>4w: Halo traction 4w as well, high chance of failure then OT x fuse C1/2 (other indications: irreducible >3 months, neurological deficit, recurrent)
431Grisel’s syndrome: drainage of inflammatory mediators through pharyngovertebral vein to periodontoid plexus → ligamentous laxity
440——
451CMT
461Remember to look for other packaging disorders
471Pathophysiology: local compartment syndrome of SCM avascular fibrous band formation
481Operation
491Presentation >1yo
501>15 deg Head tilt, lag, with tumour
510yesFailed conservative management x 6m
521Unipolar (sternal head <3, sternal + clavicular head 3-10)
531Bipolar in > 10 year
541(alternative is Z plasty)
551Bipolar release in a nutshell
5612cm incision below mastoid, strip attachment from bone
5712cm incision above the sterno-clavicular jx, incise platysma, then cut both heads of SCM together w/ the deep fasica;
580yesPostop:
591Intensive stretching for 3 months
601>2yo → add adjustable torticollis brace for 3 months
610yesDangers in bipolar release?
621Surface – greater auricular nerve
631Underneath – CNXI
641Anterior - facial nerve
650yesEvidence on CMT:
661Cheng 2001 JBJS
671800 patients < 1yo onset
68195% good response to physiotherapy (address flexion, rotation, tilting), mean FU 4.5 yr
691Poor prognostic factors: >15deg rotation deficit, SCM tumor, late presentation (present >1yo)
700——
710yesTorticollis causes:
720yesCongenital: (usually painless):
731CMT, Klippel Feil
740yesAcquired:
751Osseous – AARI (trauma, tumor, infection, odontoid hypoplasia in Down’s and Achondroplasia, JRA/RA) (usually painful)
761Non Osseous – ENT, eye (Squint), CNS (Arnold chiari), Postural (usually painless), neck burns
770yesChild more likely to have AADI:
781Capsular laxity due to hormonal cause
791Facet more transverse