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Surgical management cleft lip and palate
1. Surgical Management of Cleft lip
and Cleft palate
Dr. Nikitha Sree. K
Lecturer
Malabar Dental
College and
Research Centre
2. Introduction
•Facial clefting is the second most common
congenital deformity
• Affects 1in 750 births
• Problems are cosmetic, dental, speech,
swallowing, hearing, facial growth, emotional
3. Embryology
Primary Palate- Triangular area
of hard palate anterior to
incisive foramen to point just
lateral to
lateral incisor teeth
– Includes that portion of
alveolar ridge and four incisor
teeth.
Secondary Palate- Remaining
hard palate and all of soft palate
4. Facial Development - 4th - 10th week of development
Formed by the fusion of five prominences
Unpaired frontonasal process
lateral/medial nasal processes
Nose/Philtrum of upper lip
Paired maxillary swellings
Cheeks/Upper lip (-philtrum)
Paired mandibular swelling
Lower face (lower lip/chin)
5. Facial Development
Medial nasal processes
(green) migrate toward each
other and fuse
Inferior tips of medial nasal
processes expand laterally to
form the intermaxillary process
Tips of maxillary swellings
(yellow) grow to meet the
intermaxillary process and fuse
6th week
7th week
Failure of maxillary
swellings to fuse with
intermaxillary process
= cleft lip
Clinical Aspects of Cleft Lip/Palate Reconstruction
6.
7. Formation of the Palate
6th week
1) As nasal pits of
lateral nasal
process
invaginate and
fuse,
intermaxillary
process extends
to form primary
palate
Clinical Aspects of Cleft Lip/Palate Reconstruction
8. 8th - 9th week
2) Medial walls of maxillary processes produce palatine
shelves
3) Shelves grow downwards, parallel to lateral suface of
tongue
4) End of week 9, rotate upward into a horizontal position and
fuse with each other and primary palate to form secondary palate
Clinical Aspects of Cleft Lip/Palate Reconstruction
9. Epidemiology
The second most common congenital anomaly
Affects 1in 750 births
The incidence of cleft lip/palate varies among different
populations
The most common in asians (1:500)
In whites (1:750)
The lowest in blacks (1:1000 or less)
Cleft lip more often in boys (left side)
Isolated cleft palate more often in girls
Young mothers are less risky
12. Genetic Factors
First child has anomaly
Probability of second child
% 4
Probability of third child % 10
Two childern have anomaly
Probability of third child % 20
Mother or Father has anomaly
Probability of first child % 5
Both mother and father have anomaly
Probability of first child % 25
13. Environmental factors
Mothers sickness during first trimester (viral
infections)
Chronic diseases ( Diabetes Mellitus etc.)
Drugs (excessive use of antibiotics, steroids and
insulin,antiepileptic drugs)
Smoking
Aspirin
X Rays
14. CLASSIFICATION
DAVIS AND RITCHIE CLASSIFICATION (1922)
Based on position of the cleft in relation to the
alveolar process:
• Group I- Prealveolar clefts –
(unilateral,bilateral,median)
• Group II- Postalveolar clefts
• Group III- Complete alveolar clefts (unilateral,bilateral,median)
15. VEAU CLASSIFICATION (1931)
• Group I: Cleft of the soft palate only
• Group II: Cleft of soft and hard
palate
• Group III: Complete unilateral cleft,
extending from uvula to incisive
foramen and then deviates to one
side extending through the alveolus
• Group IV: Complete bilateral
alveolar cleft
16. • Areas 1 and 4 – Lip
• Areas 2 and 5 –Alveolus
• Areas 3 and 6 –Palate between the
alveolus and the incisive foramen
• Areas 7 and 8 –Hard palate
• Area 9 – Soft palate
Kernahan and Stark symbolic classification
17. 1 & 5 - Floor of nose on right & left sides
2 & 6 - Lip
3 & 7 - Alveolar ridges
4 & 8 - Premaxilla to incisive foramen
9 & 10 - Each half of the hard palate
11 - Soft palate
12 - Congenital velopharyngeal incompetence without obvious clefts
13 - Protrusion of premaxilla
18. Problems in Cleft Lip and Cleft
Palate
• Feeding
• Speech problems
• Frequent upper respiratuary tract infection
• Otitis media
• Nasal regurgitation of food
• Aspiration pneumonia
• Growth retardation
• Dental problems
• Psycological problems (family)
21. Surgical correction of orofacial
clefts
Lip adhesion- 1 month
Definitive lip repair- 4-6 weeks
Cleft palate repair- 12-24 months
Alveolar grafting- 8-11 years
Orthognathic surgery + cleft nose repair- 17-18
years
Final prosthodontics- 17-19 years
22. Lip repair
Timing of lip surgery
• Millard’s Rule of 10
10 weeks of age
10 gm of Hb
10 pounds of weight
Recently- 4-6 weeks
23. Lip adhesion procedure
Done at the age of one
month old
Only the cleft lip margins
were sutured without
involving muscular
component.
Re modelling of maxilla
take place and assist in
feeding.
Additional surgical
procedure is needed.
24. Rose-Thompson operation or straight
line repair
Edges of cleft are excised and
approximated in a figure of eight
sutures.
Rose used curved incisions with
concavities and Thompson used
straight incisions running
obliquely across the lip to gain
length.
Indicated in incomplete and
narrow clefts.
25. Tennison triangular flap
Tennison in 1952 used the height of the normal side of the
lip for estimating the repaired side.
A wire bent into a Z shape, the two sides were marked to
give a method of measurement that is simple, preserves the
cupid bow and gives a zig zag scar, which helps to hide the
scar.
A cut is made to correct the upward tilt of cupid’s bow on the
lower one third of the lip, the gap is later filled with a triangle
of skin ,muscle and mucosal flap from the lower end of
lateral lip element
26.
27. Advantages
• Cupid’s bow is brought from its angulated, upright
position to a level one.
• The added tissue on medial side gives a natural
protrusion in this area.
• The zig zag scar hides the line from the vermilion to the
nasal floor.
Disadvantages
• Philtral column is not restored
• May produce a lip that is too long.
28. Millard rotation advancement repair
Used in complete, incomplete and wide cleft lip
repairs.
In this repair ,the tilted cupid’s bow is rotated down
following a curved incision extending under the
columella. The high rotation gap created will be filled
with a triangular flap comprising skin ,muscle and
mucosa
The resultant scar is hidden under the nose and
follows the line of philitrum.
29.
30. Advantages
• The resultant scar follows natural lines in the lower half
of the lip and provides a scar that is simple to revise.
• Preserves cupid’s bow and philitral dimple.
• Preserves pleasing outward pointing of the lower
portion of the lip.
Disadvantages
• Difficult to get adequate rotation and optimal lateral flap
in wide cleft lip.
31. Palate repair
The hard palate is supported by bony shelves
with mucosal coverings ,while the soft palate
consists of muscle with mucosal covering.
TIMING OF REPAIR
Most surgeons close the soft and hard palate
as early as 6 – 9 months of age and almost
always before 18 months of age.
32. Primary veloplasty
Introduced by Schweekendick
Soft palate is closed at an early stage(6-12
months) and hard palate is closed few years later.
Principle behind this technique is that softpalate
aids in speech and essential to be closed early
for velopharyngeal mechanism.
But it seen to cause severe speech problem due
to scarring and shortening of softpalate. So it is
rarely indicated.
33. Von Langenbeck’s palatoplasty
It is a side to side approximation of the cleft margins
of both the hard and soft palate, with detachment of
the levator muscles from their bony insertions and
use of long relaxing incisions laterally to close the
hard palate without tension.
34. Wardill –kilner- V-Y Palatoplasty
An incision is placed to enable v-y closure.
This includes lateral relaxing incision and bilateral
island flaps based on the posterior palatine arteries.
Soft palate is also incised along the margins and
oral and nasal layers are seperated.
Nasa layers are sutured and soft palate is closed in
3 layers.
Lengthens palate and better velopharyngeal seal,
which allows better speech.
35.
36. Alveolar Grafting
Placement of bone graft during the eruption of
permanent canine(8-11 years)
Bone harvested is mainly from cancellous bone of
iliac crest, and packed tightly in to the defect.
37. Orthognathic surgery
Facial deformity is corrected at the age of 17-18
years, after the growth completion.
Maxillary advancement by orthognathic surgery or
by distraction osteogenesis.
Mandibular retrusion may also be done
38. Cleft nose repair
Cleft nose requires correction and rhinoplasty at a
much later stage of growth of the patient
Final prosthodontics
From 17-19 years, final implant placement for the
missing lateral incisors may be done.
39. Reference
Textbook of Oral and Maxillofacial Surgery- Chitra
Chakravarthy
Textbook of Oral and Maxillofacial and Surgery-
Neelima Anil Malik