100%(3)100% ont trouvé ce document utile (3 votes)
611 vues54 pages
Cleft lip and cleft palate are congenital abnormalities where the lip or roof of the mouth do not fully form during development. In the past, they were thought to be caused by evil spirits or solar eclipses affecting the pregnant woman, but now are understood to have multiple genetic and environmental causes. A multi-disciplinary team approach is used for treatment, involving specialists like plastic surgeons, pediatricians, dentists, orthodontists and speech therapists to address issues from infancy through adulthood. Left untreated, cleft lip and palate can cause problems with feeding, speech, dental development and psychological impacts; however with proper treatment and management by a team of experts, affected individuals can now lead happy and functional lives
Cleft lip and cleft palate are congenital abnormalities where the lip or roof of the mouth do not fully form during development. In the past, they were thought to be caused by evil spirits or solar eclipses affecting the pregnant woman, but now are understood to have multiple genetic and environmental causes. A multi-disciplinary team approach is used for treatment, involving specialists like plastic surgeons, pediatricians, dentists, orthodontists and speech therapists to address issues from infancy through adulthood. Left untreated, cleft lip and palate can cause problems with feeding, speech, dental development and psychological impacts; however with proper treatment and management by a team of experts, affected individuals can now lead happy and functional lives
Cleft lip and cleft palate are congenital abnormalities where the lip or roof of the mouth do not fully form during development. In the past, they were thought to be caused by evil spirits or solar eclipses affecting the pregnant woman, but now are understood to have multiple genetic and environmental causes. A multi-disciplinary team approach is used for treatment, involving specialists like plastic surgeons, pediatricians, dentists, orthodontists and speech therapists to address issues from infancy through adulthood. Left untreated, cleft lip and palate can cause problems with feeding, speech, dental development and psychological impacts; however with proper treatment and management by a team of experts, affected individuals can now lead happy and functional lives
Dr. Ritu Jindal Submitted By : Dr. Jasvi Shergill Ravi Sher Singh Toor Dr. Sandeep Mahajan MDS 1 st year (2007) Dr. Rohini Dua Dept.of Pedodontics.
Definition
It can be defined as congenital abnormal gap in the palate that may occur alone or in conjunction with lip and alveolus cleft.
Ancient times It was considered to be due the effect of evil powers or solar eclipse on a pregnant woman .
Some tribes considered it to be a blessing and were supposed to bring fortune to the family.
Now a days cleft lip and cleft palate baby leads a happy life in the society without much esthetic or functional deficiencies.
How it happens ? In the early weeks of development, long before a child is born, the right and left sides of the lip and the roof of the mouth normally grow together.
Occasionally, however, in about one of every 800 babies, those sections don't quite meet.
A child born with a separation in the upper lip is said to have a cleft lip.
A similar birth defect in the roof of the mouth, or palate, is called a cleft palate.
Since the lip and the palate develop separately, it is possible for a child to have a cleft lip, a cleft palate, or variations of both. Development of palate Embryological development of palate can be divided into two parts.
Development of primary palate It includes lip and the area anterior to the incisive foramen. It develops from the fusion of maxillary and medial nasal process.
Development of secondary palate It includes the plate behind the incisive foramen. The palatal shelves are formed by contribution of maxillary and frontonasal process. The maxillary process gives off two offshoots called as palatal shelves that grow medially towards each other. The union of these two shelves is prevented by the tongue, there by leading to downward growth of the shelves. The tongue descends down by 81/2 weeks which results in the close proximal relation of the two shelves, complete fusion occurs by 12 weeks.
A- Palatine shelves are forming from the maxillary processes and directed downwards on each side of the tongue. B- Tongue has been depressed and the palatine shelves have been elevated but not fused. C- Fusion of the shelves and the nasal septum is completed. Pathogenesis of clefting Various theories and mechanisms have tried to explain the development of cleft lip and cleft palate. Some of them are:
Dursy- (Hypothesis): Failure of fusion between median nasal and maxillary process. Veaus Hypothesis: Failure of in-growth of mesoderm between the two palatal shelves. Excessive head width or diminutive palatal shelves. Alterations in intrinsic palatal forces. Excessive tongue resistance. Non fusion of shelves. Fusion of shelves with subsequent breakdown. Failure of tongue to drop down as in case of Pierre Robin syndrome. Inclusion cyst pathology. Incidence of cleft Overall incidence varies from 0.3 to 6.5 per 1000 live births.
Negroid race has least incidence while mongoloid have the maximum.
Cleft lip is more common in males.
Cleft palate is more in females.
Unilateral clefts are more common as compared to bilateral.
Left side is more predisposition for clefts.
Incidence is increased with increase in parental age.
More chances of cleft in patients with family history of the same. Etiology of cleft lip and palate. Some of the postulated reasons are : Heredity - Defect seems to run in families. Environment Teratogens like rubella virus, thalidomide. Mutant genes Some syndromes follow Mendelian inheritance. E.g. Lobster defect-cleft with ectodermal dysplasia. Chromosomal aberrations- Cleft can occur with many cromosomal defects like trisomy 21. Increased maternal age. Decreased blood supply in naso-maxillary region. Defeciency of folic acid and vitamin A. Multifactorial inheritance- recent studies have shown that cleft cannot be attributed to one single factor and is conglamation of multiple genetic and environmental factors.
Classification of cleft lip and Palate Davis and Ritchies Classification : (1922)
Pre alveolar clefts-unilateral, bilateral and median. Alveolar clefts-complete cleft involving palate, lip, and alveolar ridge. Post alveolar cleft- comprises of different degrees of hard and soft palate clefts up to the alveolus. Veaus Classification (1931)
Group 1- Clefts of small palate only. Group 2-Cleft of hard and soft palate upto incisive foramen. Group 3-Complete unilateral clefts involving lips, hard palate, soft palate and the alvelous. Group 4-Complete bilateral clefts involving lips, hard palate, soft palate and the alvelous.
Veaus Cleft Palate Veaus Cleft Lip Fogh Andreasons classification: (1942) Group 1- Clefts of lip. Group 2 Clefts of lip and palate. Group 3 Clefts of palate upto incisive foramen.
Schuchard & Pfeiffers Classification : Symbolic Classification in which different regions are depicted and then are shaded according to the type of cleft depending on weather its total or partial Kernahans Stripped Y Classification (1972) This is a symbolic classification in which numbering is given to each site representing the oral cavity. The shaded area denotes presence of cleft in the particular area. Embryological Classification Kernahan, Stark (1958) and Spina (1974) They have classified cleft lip and palate depending on the embryological principals. Kernahan and Stark classification: Group I : Cleft of primary palate only. Unilateral, Bilateral, Total, Subtotal. Group II : Cleft of the secondary palate only. Total, Subtotal, Submucous. Group III : Cleft of both primary and secondary palate Unilateral, median, Bilateral Spinas Classification: Group I: Pre-incisive foramen clefts. Unilateral, Bilateral, Median. Group II: Trans incisive foramen clefts. Unilateral, bilateral. Group III: Post Incisive Foramen clefts. Total, Partial. Group IV: Rare facial clefts.
Types of cleft lips and Palates. A- Normal anatomy E-Group II complete. B-Group I Unilateral F-Group III unilateral. C-Group Ia unilateral G-group III bilateral. D-Group Ia bilateral Millards Modification of stripped Y (1976) He added another parameter to the Kernahans classification and that was addition of nasal floor. LAHSHALs Classification This was given by Okriens in 1987, He developed a paraphrase for each area and the cleft could be denoted as such.
L - Lip H Hard palate A Alveolus A - Alvelous H Hard palate L - Lip S Soft palate
Clinical Features: Chief Complaint Deformity of Face. Unable to feed. Nasal regurgitation of fluids.
Congenitally missing teeth. Neonatal teeth. Ectopic Eruption. Supernumerary teeth. Dental Problems Micro & Macrodontia. Fused teeth. Anomalies in tooth size and shape Enamel hypoplasia. Deep bite / Cross bite. Crowding / Spacing of teeth. Esthetic Concerns Loss of Facial Morphology Missing Structure
Disorders of middle Ear. Hearing and Speech Pathology Nasal Twang in Voice. Difficulty in articulation.
Psychological effects. Due to the defect the patient are object of curiosity, pity and often are separated from their normal counterparts which can lead to a social and mental trauma.
Until the foundation of Lancaster cleft palate clinic in Pennsylvania, Independent clinicians carried out the treatment of children with clefts. The patient had to go from one clinic to the other for correction. Later it was Copper who came up with an idea that all clinicians providing treatment to the child can act as a team.
Multi-disciplinary team for cleft lip and palate patients. Obstetrician Refers the child to plastic surgeon/pediatrician Counseling the parents.
Pediatrician Provides medical care. Refers the case to plastic surgeon.
Plastic Surgeon Heads the team, discusses the case monthly. Carries out initial lip repair and palate surgery. Performs phyrangoplasty and nose surgery.
Oral maxillofacial Bone grafting Surgeon If any orthopedic surgery is, performed at later stage
Neurosurgeon if any craniofacial syndrome is associated.
Pedodontist A key member who sees the baby and the parent at the time of repair of the lip. Provides presurgical orthopedic treatment. Monitors the growth and development. To maintain perfect oral health. To guide the occlusion and facial growth. Motivates the parent and the child.
Orthodontist Provides pre surgical consultation. Carries out definitative orthodontic treatment in the permanent dentition.
Speech Pathologist Monitors the speech development to normal.
Audiologist To test hearing in the baby, infant and child.
Otolaryngologist Concerns with the health of nasopharyngeal tissues, including tonsils, adenoids and middle ear structures.
Psychologist Plays an important role when the childs family is under stress.
Protocol for Dental Care of Cleft Lip and Palate in Children. Protocol is developed to provide a comprehensive treatment in alliance with other experts to attain optimal treatment in the cleft lip & palate patient.
At birth Attend referral Predental treatment Feeding plate. Pre-surgical orthopedics. Help surgeon in repair by stimulating palatal bone growth and preventing collapse of dental arches. Make study records by photographs, models.
3-5 Months. Introduce the parents to dental care for the primary teeth. Alignment of primary teeth and palatal expansion to be started using a simple fixed appliance like W-arch and Arnold expander. Plastic surgeon to repair the lip. Audiology, ENT surgeon to repair the lip. Suction myringotomy for glue ear
Arnold expander
12 Months Pedodontic review, palatal prosthetic speech appliance may be required to correct velopharyngeal incompetence. Explain possible eruption abnormalities. Plastic surgeon to repair the palate. Speech pathology first assessment. Review by audiologist and ENT surgeon. 2-6 years Pedodontist should review facial growth and development with regular monitoring at one year interval. Preventive measures for caries like fissure sealants, fluoride application. Restorative if needed. Plastic surgeon to review every 12 months.
6-7 years Pedodontist to review the case. Preventive or early orthodontic intervention (like removal of supernumerary teeth, correction of cross bite) Radiographic evaluation (special occlusal view) Orthodontic consultation.
8 years. Suitability about bone grafting. Dental bone assessment (OPG, Cephalogram) Review by plastic surgeon, speech pathologist and ENT surgeon. Pedodontist to review if orthodontic intervention is needed.
9 years Combined orthodontist and pedodontist coalescence. Bone graft alveolar cleft at half to one-third root development of permanent cuspid. Review by other experts.
10-12 years Pedodontist to plan future treatment. Orthodontic consultation. Monitoring changing dentition and growth. Preventive measures with a review of dental health
12-15 years Orthodontic treatment Pedodontic review at yearly intervals regarding other dental treatments. Oral surgeon to assist if orthodontist requires. Review by plastic surgeon Speech pathologist to review. Management of cleft lip and palate Patients For successful treatment of the patient with cleft lip and palate some pre- requisites are necessary before the comprehensive treatment can be initiated. These are:
Parent Counseling: The most important people associated at this stage are parents. They need support and information regarding the treatment aspects. It is important to negate fears and guilt regarding the child that a parent may have. Mother plays important part in the form of a nurse as well as a mother. Nursing management: After the obturator has been fitted the mother will take care of this appliance. After each feed the plate is removed and cleaned with running water and soaked once a day for 20 min. in Hibitane solution. Feeding management:
Children having cleft palate face inability to feed, as the child is not able to create negative pressure required for suckling of milk from the mothers breast. which is solved by using breast pumps, obturators, and spoon feeding. Another problem is regurgitation of milk through the nose, which can be solved by rising the childs head around 45 degrees. Cleft lip Repair Timing : Rule of 10 (Hb. 10gm%, age 10 weeks, weight 10 lbs., TLC < 10,000 per cc mm.)
Types of cleft lip surgery For unilateral: (common) Millards rotation advancement flap, Tennison-Randall Triangular flap. Less frequently used are: Rose thompson Stright line repair Skoogs procedure. For bilateral: Single stage by Veaus III Procedure Millard single stage Procedure
Basic steps in cleft lip repair.
Aim Achieve equal length of philtral ridges horizontal cupids bow accurate repair of muscle, skin, mucosa maintain vermilion border as much as Possible Symmetrical nostril floor & aesthetics Millards Repair: The rotational flap (a) ; Columella flap (c) are planed on the median side of the cleft. After full thickness of the lip is cut along the marking, a rotation gap is produced on the medial side which is filled by an advancement flap (b) planned on the lateral side of the cleft.
In this minimal tissue is discarded and the result can be modified during the surgery. Tennision Randall repair. A triangular flap is created on the lateral side of the cleft to fit into the triangular defect produced on the median side of the cleft. It can be performed only after initial measurements. The result cannot be modified once the lip is cut. The scar is more prominent. Veaus III. repair It is the simplest one straight line closure and having satisfactory results in bi lateral cleft lip. The vermilion flap from either lateral side of the cleft is brought down over the pro labium to augment the vermilion in the center of the upper lip Cleft palate repair Timing: Experience of most of the surgeons show that repair of palate between 12-18 months of age gives best results.
Types of cleft palate repair: Cleft palate is repaired by mucoperiosteal flaps. There are two ways: Single stage repair (Von langenbeck repair & Ven wardill Kilner): -At the age of 18 months. -V-Y push back palatoplasty, produces normal speech in 50-70% cases, But midfacial growth retardation problem is not solved. -Repair by double opposing Z-plasty of Furlow is a new procedure aimed at reducing the midfacial growth retardation problem. Two stage repair: First Stage- Soft palate repair before 18 months followed by obturation of hard palate till the second stage repair. Second stage repair- At 4-5 yrs. Hard palate repair.
This Schweckendiek two stage procedure allows better midfacial growth, but speech results have been not so good. Veau-Wardill-Kilnar V-Y Pushback platoplasty : -Two mucoperiosteal flaps are raised from the hard palate and nasal layers are mobilized.
-Abnormal attachment of palatal muscles are divided from the posterior border of the hard palate to be sutured in midline to the opposite side of the palatal muscles. (intravelarveloplasty)
- Suturing is started from anterior end of the nasal layer and progressed towards the uvula.
Two flap palatoplasty (diagrammatic representation) Pre-Dental Treatment Feeding plate if required? Decision regarding assisting the surgeon should be left to the surgeon. To stimulate palatal bone growth and to restore orofacial functional matrix To Expand or prevent the collapse of maxillary segment.
Primary dentition treatment: Proper alignment and/or expansion of the primary dentition can be done more easly. Simple form of fixed maxillary lingual appliance (i.e either a W- arch or an arnold expander) are preferred over the removable split palatal type of appliance because of high relapse rate with removable appliance. Mixed dentition treatment Various problems which require attention at this stage, these are: Minor cross bites. Corrected by expansion by usual methods, once complete then retention is required.( because there is no mid palatal suture system to fill the bone and consolidate the expanded maxillary segments).
Retro inclination of permanent incisors and anterior cross bite. This can lead to esthetic, speech and psychological problems. To correct this partial banded approach is needed, after correction full time retention is needed.
Crowded dentition. Serial extraction may be required, primary cuspids are removed to treat incisor crowding and primary molars may be removed to hasten the eruption of the first bicuspids.
Alveolar bone grafting. Alveolar bone grafting is done just before canine erupts.
Correction of anterior & posterior cross bite in the deciduous & mixed dentition. a. Complete unilateral cleft lip & palate (un operated) b. Palatal segments in contact. c. Palatal cleft closed at 6 months of age. d. Bilateral buccal and anterior cross bite. e. Arnold expander is in place f. Cross is still present due to excessive scar. g. Expander is fully extended in early mixed dentition. h. Anterior cross bite was corrected, but buccal cross bite is still present. Alveolar Bone Grafting.
Aim Restore the bony contour of the alveolus Stabilize the maxillary expansion Provide a matrix through which the Teeth may erupt Allow the teeth to have a healthy supporting peridontium
Alveolar bone grafting Involves:
Pre surgical Palatal expansion (if required) with fixed appliances such as quard helix Preparation of recipient area by extraction of retained primary teeth several weeks before surgery. Bone harvest for the graft is usually autologous illiac crest corticocancellous bone, but must be obtained from the mandibular symphsis, tibia, rib or calvarium. The procedure may include revision of lip and /or palate repair if necessary and will definitively close any remaining fistulae.
Samman et al. (1994) showed that timing of the operation, preoperative gingival health and careful tissue and graft handling during surgery are more important in determining the success of the operation than the anatomical source of the bone graft. Before After surgery Periapical radiograph of a cleft bone grafting. Lateral incisor is present on the palatal aspect of the canine tooth. Also present is a small supernummary tooth (arrowed), was removed at the time of surgery. The cleft is been filled with cancellous bone, harvested from illiac crest. After 3 months there is movement of lateral and canine and both these teeth are erupted through the graft into the mouth, and were aligned orthodonticaly. Bone grafting Bone grafting case before.
After 3 months. Permanent Dentition Treatment: In mixed dentition, only the minimum of active orthodontic treatment (if any) is done, leaving the bulk of the treatment to be carried out in the shortest possible time when full permanent dentition is present. At 12-16 yrs. Dental suitability and motivation to cooperate with the orthodontic treatment is assessed. Rapid palatal expansion and/or fixed orthodontic therapy is undertaken at the optimum time- occasionally elective extraction of teeth is indicated. Further orthodontics, in conjunction with orthognathic surgery may be required in the event of significant skeletal dysplasia. Definitative orthodontic treatment once active, the skeletal growth ceases Pre and post surgical orthodontics in conjuction with orthognathic surgery. Orthognathic Surgery
If maxillary / mandibullar skeletal discrepancy exists at the time of physical maturity an osteotomy may be required along with any soft tissue revision. A Le Fotre I osteotomy with modification my be performd to correct occlusion and facial appearance.( Tideman et. El.1980). More severe skeletal deformities require a staged procedure involving a Le Forte II, Subsequently a Le Forte I osteotomy followed by a mandibular procedure.
If necessary, an esthetic rhinoplasty and cheiloplasty should be performed as a final surgical stage. Occasionally, however functional lip and nose revision is combined with alveolar bone grafting at an earlier stage to reduce the impact of the aesthetic deformity on the growing child.
The above procedures are only some of the many that are needed by a patient with cleft lip and palate.
A . Patient shown is 15 yrs. The nasal tip is broad and deviated. B. Lateral view shows mid facial retrusion from infraorbital rims to dentition, with poor support from upper lip. C. Intra oral view of ant. Cross bite. D. Lateral cephalogram demonstrates class III malocclusion, and anterior cross bite. E. Lateral cephalogram 2 yrs. After le fort I osteotomy/maxillary advancement and malar implants. F. 2 yrs. after maxillary advancements, insertation of malar implants, elevation of left alar cartilage, sepetal resection and nasomaxillary osteotomies. G. Harmonious sagittal relationship. H. Intra oral view after completion of ortho. treatment. Conclusion
The successful habilitation of the child born with cleft lip and palate requires close cooperation among the many specialist on a high volume team.
A coordinated approach is preferred to help the child achieve ideal speech, occlusion, facial appearance, and self esteem.
Providing the patient with the ability to pursue and achieve personal success in life without particular regard to the original cleft deformity is the ultimate goal.
Pictures: Cleft Lip
Pictures: Cleft Palate References Handbook of pediatric dentistry by Cameron, Widmer. Text book of pediatric dentistry by S.G. Damle. Text book of pedodontics by Shobha Tandon. Pediatric oral and maxillofacial Surgery by Leonard B. Kaban, Maria J. Troulis. www.Pubmed.com www.cleftlip.com www.webmd.com www.widesmiles.com