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ACHEBE JU
HONORARY CONSULTANT PLASTIC SURGEON
UNTH
 Common congenital abnormality of the face
 Involves the lips, nose and mouth
 Produces functional or aesthetic problems or
both
 Structures that will form the face present about
4-6wks of gestation
 Frontonasal process, paired maxillary and
mandibular prominences
 Bilateral nasal placodes form from the
frontonasal process
 They have medial and nasal processes
 Upper lip formed by fusion of medial nasal
process with each other and maxillary
prominence
 These events occur in the first trimester.
 Structures destined to form the palate by
8wks
 Two palatal shelves of the maxilla, initially
vertical with the tongue in between
 Palatal shelves rotate to become horizontal
while the tongue descends
 Palatal shelves start fusion from in front and
proceeds backwards
 Failure of fusion
 Lack of mesodermal infiltration after fusion
 both
 CLEFT LIP --unilateral- complete or incomplete
 bilateral -complete or incomplete
 median
CLEFT OF THE PALATE----- extent
 CLEFT OF THE LIP AND PALATE—unilateral or
bilateral—complete or incomplete
 SUBMUCOUS CLEFT.
 Cleft of primary palate anterior to incisive
foramen –eg cleft lip
 Cleft of the secondary palate- posterior to
incisive foramen-eg cleft palate
 White ancestry : 1 in 1000 live births
 Asian ancestry : 1 in 500 live births
 African ancestry : 1 in 2000 live births
 Cleft palate no racial bias 1:2000 live births
 White population CLP > CP > CL
 NIGERIA 8o’s CL > CP > CLP
 NIGERIA now CLP > CL > CP
 CL and CLP different entity from CP
 CL and CLP more common on the left and
males
 Isolated cleft palate more common in females
 Associated anomalies including syndromes
more common in CP
Environmental teratogens
phenytoin
steroids
alcohol
smoking
GENETIC FACTORS
positive family history
syndromes with cleft—Van der Woudes
pierre robin sequence
velocardiofacial syndro
trisomy 21
Cleft lip and cleft lip and palate gentically different from isolated
Cleft palate
 From childhood to adult
 Multidisciplinary team
 PLASTIC SURGEON
 ORAL SURGEON
 ENT SURGEON
 ORTHODONTIST
 PEDIATRICIAN
 SPEECH THERAPIST
 CHILD PSYCHIATRIST
 PEDIATRIC NURSES
 History antenatal , family and social history
 Immediate problem feeding, and airway
 Nasal regurgitation of food
 Examination also look for associated abnormality
 Examine the mouth
 Baseline investigation
 Clinical photograph
 Reassure parents and outline management
programme
 Submucous clefts could be missed
 ANTENATAL ULTRSOUND SCAN
For cleft palate assess the ear
Higher incidence of sensorineural and
conductive hearing loss
 MICROGNATHIA
 CONGENITAL HEART DISEASE
 LIMB ABNORMALITIES
 LIP PITS
 CONGENITAL HERNIA
 Cleft lip from 3months
 Cleft lip and palate lip repair as from 3mths
palate repair 10-12mths
Cleft palate palate repair 10-12mths
Pierre Robin’s sequence palate 18 months
 RULE OF TEN
 >10wks
 >10 Ibs
 >10gms
 Normal appearance of lip, nose and face
 Normal speech
 Normal dentition
 Normal facial development
 PRE-OP EVALUATION
 DEFORMITY
 RULE OF TEN
 CLEFT
 ORBICULARIS ORIS
 NASAL DEFORMITY
 MAXILLARY
HYPOPLASIA
 DENTAL PROBLEM
 ROTATION ADVANCEMENT TECHNIQUE
[MILLARD]
 STRAIGHT LINE CLOSURE
 ASSOCIATED
PROBLEM
 SPEECH
 MIDDLE EAR
INFECTION
 PIERRE ROBIN
SYNDROME
 FEEDING PROBLEM
 Adequate mechanism
 Hearing
 Intelligence
 Stimulating environment
 consonants
 Hyper nasality
 Nasal escape
 Omission
 substitution
 Poor aeration of middle ear
 Secretory otitis media with hearing loss
 Myringotomy and ventilating tubes
 10mths ----- 12mths
 PRE-OP ASSESMENT
 TIMING OF REPAIR
 METHOD OF REPAIR
 V-Y PALATOPLASTY
 LANGENBECH PALTOPLASTY
 FURLOW TECHNIQUE
 BARDACH TECHNIQUE
 HEMORRAGE
 AIR WAY OBSTRUCTION
 BREAK DOWN OF REPAIR
 FISTULA
 VPI
 MAXILLARY HYPOPLASIA
 History
 Physical exam
 Nasendoscopy
 videofluroscopy
 REVISION OF LIP 4-6yrs
 PHARYNGOPLASTY 6-9yrs
 ALVEOLAR BONE GRAFT 8-11yrs
 MAXILLARY OSTEOTOMY 15-18yrs
 ORTHODONTIC PROCEDURE
 RHINOPLASTY 15-18yrs
 LACK OF OTHER SPECIALISTS IN THE CLEFT
TEAM
 Speech language pathologists
 Orthodontists
 Maxillofacial surgeons interested in clefts
 Limited involvement of ENT surgeons in cleft
care
 Poor follow up
 poverty
 Functional reconstruction of cleft lip
 Functional reconstruction of cleft palate
 Primary nasal repair at the time of lip repair
 Charity organizations that sponsor cleft care
in the developing countries
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CLEFT LIP AND PALATE.pptx

  • 1. ACHEBE JU HONORARY CONSULTANT PLASTIC SURGEON UNTH
  • 2.  Common congenital abnormality of the face  Involves the lips, nose and mouth  Produces functional or aesthetic problems or both
  • 3.
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.
  • 9.
  • 10.
  • 11.
  • 12.
  • 13.
  • 14.
  • 15.
  • 16.
  • 17.
  • 18.
  • 19.
  • 20.
  • 21.
  • 22.
  • 23.
  • 24.
  • 25.
  • 26.
  • 27.  Structures that will form the face present about 4-6wks of gestation  Frontonasal process, paired maxillary and mandibular prominences  Bilateral nasal placodes form from the frontonasal process  They have medial and nasal processes  Upper lip formed by fusion of medial nasal process with each other and maxillary prominence  These events occur in the first trimester.
  • 28.
  • 29.
  • 30.  Structures destined to form the palate by 8wks  Two palatal shelves of the maxilla, initially vertical with the tongue in between  Palatal shelves rotate to become horizontal while the tongue descends  Palatal shelves start fusion from in front and proceeds backwards
  • 31.  Failure of fusion  Lack of mesodermal infiltration after fusion  both
  • 32.  CLEFT LIP --unilateral- complete or incomplete  bilateral -complete or incomplete  median CLEFT OF THE PALATE----- extent  CLEFT OF THE LIP AND PALATE—unilateral or bilateral—complete or incomplete  SUBMUCOUS CLEFT.
  • 33.
  • 34.  Cleft of primary palate anterior to incisive foramen –eg cleft lip  Cleft of the secondary palate- posterior to incisive foramen-eg cleft palate
  • 35.  White ancestry : 1 in 1000 live births  Asian ancestry : 1 in 500 live births  African ancestry : 1 in 2000 live births  Cleft palate no racial bias 1:2000 live births
  • 36.  White population CLP > CP > CL  NIGERIA 8o’s CL > CP > CLP  NIGERIA now CLP > CL > CP  CL and CLP different entity from CP  CL and CLP more common on the left and males  Isolated cleft palate more common in females  Associated anomalies including syndromes more common in CP
  • 37. Environmental teratogens phenytoin steroids alcohol smoking GENETIC FACTORS positive family history syndromes with cleft—Van der Woudes pierre robin sequence velocardiofacial syndro trisomy 21 Cleft lip and cleft lip and palate gentically different from isolated Cleft palate
  • 38.  From childhood to adult  Multidisciplinary team
  • 39.  PLASTIC SURGEON  ORAL SURGEON  ENT SURGEON  ORTHODONTIST  PEDIATRICIAN  SPEECH THERAPIST  CHILD PSYCHIATRIST  PEDIATRIC NURSES
  • 40.  History antenatal , family and social history  Immediate problem feeding, and airway  Nasal regurgitation of food  Examination also look for associated abnormality  Examine the mouth  Baseline investigation  Clinical photograph  Reassure parents and outline management programme  Submucous clefts could be missed  ANTENATAL ULTRSOUND SCAN
  • 41.
  • 42.
  • 43.
  • 44.
  • 45.
  • 46.
  • 47. For cleft palate assess the ear Higher incidence of sensorineural and conductive hearing loss
  • 48.  MICROGNATHIA  CONGENITAL HEART DISEASE  LIMB ABNORMALITIES  LIP PITS  CONGENITAL HERNIA
  • 49.
  • 50.
  • 51.  Cleft lip from 3months  Cleft lip and palate lip repair as from 3mths palate repair 10-12mths Cleft palate palate repair 10-12mths Pierre Robin’s sequence palate 18 months
  • 52.  RULE OF TEN  >10wks  >10 Ibs  >10gms
  • 53.  Normal appearance of lip, nose and face  Normal speech  Normal dentition  Normal facial development
  • 54.  PRE-OP EVALUATION  DEFORMITY  RULE OF TEN  CLEFT  ORBICULARIS ORIS  NASAL DEFORMITY  MAXILLARY HYPOPLASIA  DENTAL PROBLEM
  • 55.
  • 56.
  • 57.
  • 58.  ROTATION ADVANCEMENT TECHNIQUE [MILLARD]  STRAIGHT LINE CLOSURE
  • 59.
  • 60.
  • 61.
  • 62.
  • 63.
  • 64.
  • 65.
  • 66.
  • 67.  ASSOCIATED PROBLEM  SPEECH  MIDDLE EAR INFECTION  PIERRE ROBIN SYNDROME  FEEDING PROBLEM
  • 68.  Adequate mechanism  Hearing  Intelligence  Stimulating environment
  • 69.  consonants  Hyper nasality  Nasal escape  Omission  substitution
  • 70.  Poor aeration of middle ear  Secretory otitis media with hearing loss  Myringotomy and ventilating tubes
  • 72.  PRE-OP ASSESMENT  TIMING OF REPAIR  METHOD OF REPAIR  V-Y PALATOPLASTY  LANGENBECH PALTOPLASTY  FURLOW TECHNIQUE  BARDACH TECHNIQUE
  • 73.
  • 74.
  • 75.
  • 76.
  • 77.
  • 78.
  • 79.
  • 80.  HEMORRAGE  AIR WAY OBSTRUCTION  BREAK DOWN OF REPAIR  FISTULA  VPI  MAXILLARY HYPOPLASIA
  • 81.  History  Physical exam  Nasendoscopy  videofluroscopy
  • 82.
  • 83.  REVISION OF LIP 4-6yrs  PHARYNGOPLASTY 6-9yrs  ALVEOLAR BONE GRAFT 8-11yrs  MAXILLARY OSTEOTOMY 15-18yrs  ORTHODONTIC PROCEDURE  RHINOPLASTY 15-18yrs
  • 84.
  • 85.
  • 86.
  • 87.  LACK OF OTHER SPECIALISTS IN THE CLEFT TEAM  Speech language pathologists  Orthodontists  Maxillofacial surgeons interested in clefts  Limited involvement of ENT surgeons in cleft care  Poor follow up  poverty
  • 88.  Functional reconstruction of cleft lip  Functional reconstruction of cleft palate  Primary nasal repair at the time of lip repair  Charity organizations that sponsor cleft care in the developing countries

Editor's Notes

  1. NORMAL LIP NOSE