1. Congenital anomalies of the facial region of the head. Cleft lip. Cleft palate. Flashcards
(40 cards)
Intro: Embryology of the Lip and Palate
The “primary palate,” which includes the nostril sill, upper lip, alveolus, and hard palate anterior to the incisive foramen, forms from fusion between the medial nasal and maxillary prominences during weeks 4 through 7 of gestation
Intro: Embryology of the Lip and Palate - Development of the Hard Palate
Development of the hard palate posterior to the incisive foramen and the soft palate, which are collectively known as the “secondary palate,” occurs during weeks 6 through 12 of gestation.
Intro: Function of Palate (1)
The normal palate functions primarily as a speech organ, but it is also intimately involved in feeding, swallowing, and breathing
Intro: Function of Palate (2)
The soft palate, or velum, together with lateral and posterior pharyngeal walls, can be conceptualized as a valve that regulates the passage of air through the nasopharynx.
Intro: Classification of Craniofacial Anomalies.
Classification 1
- Clefts
Intro: Classification of Craniofacial Anomalies.
Classification 2
- Synostoses: The term “craniosynostosis” refers to premature fusion of one or more calvarial sutures.
Intro: Classification of Craniofacial Anomalies.
Classification 3
- Atrophy–hypoplasia
Intro: Classification of Craniofacial Anomalies.
Classification 4
- Hypertrophy–hyperplasia–neoplasia
Development of Face
Face develops from median nasal process, lateral nasal process, maxillary process, mandibular arch, globular arch, olfactory pit and eye.
Any change in the development or
fusion of these arches leads to formation of different types of cleft lip or cleft palate.
Etiology of Cleft Lip and Cleft Palate.
Etiology (1)
Familial—more common in cleft lip or combined cleft lip and palate (Risk is 1:25
live births).
Etiology of Cleft Lip and Cleft Palate.
Etiology (2)
Protein and vitamin deficiency.
Etiology of Cleft Lip and Cleft Palate.
Etiology (3)
Rubella infection.
Etiology of Cleft Lip and Cleft Palate.
Etiology (4)
Radiation.
Etiology of Cleft Lip and Cleft Palate.
Etiology (5)
Chromosomal abnormalities.
Etiology of Cleft Lip and Cleft Palate.
Etiology (6)
Maternal epilepsy and drug intake during pregnancy (steroids/ eptoin/diazepam).
Classifications of Clefts
Classification 1
I. Cleft lip alone: Unilateral, Bilateral, Median.
II. Cleft of primary palate (in front of incisive foramen) only:
a. Complete—means absence of pre-maxilla.
b. Incomplete—means rudimentary pre-maxilla: Unilateral, Bilateral, Median.
III. Cleft of secondary palate (behind the incisive foramen) only:
a. Complete—nasal septum and vomer are separated from palatine process.
b. Incomplete.
c. Submucous: It can be - Cleft with soft palate involvement. - Cleft without soft palate
involvement.
IV. Cleft of both primary and secondary palates.
V. Cleft lip and cleft palate together.
Classifications of Clefts
Classification 2
Veau classification - The most clinically useful system to describe cleft palate morphology
A Veau I cleft is midline and limited to the soft palate alone.
A Veau II cleft may extend further anteriorly to involve the midline of the posterior hard palate (the “secondary palate”).
A Veau III cleft is a complete unilateral cleft of primary and secondary palates, in which the cleft extends through the lip, the alveolus, the entire length of the nasal floor on the cleft side, and the midline of the soft palate.
Veau IV clefts are bilateral complete clefts of the primary palate that converge at the incisive foramen and continue posteriorly through the entire secondary palate.
Not included in the Veau classification is the submucous cleft palate, which occurs when there is clefting of the soft palate musculature beneath intact mucosa.
Submucous cleft palate classically presents as the triad of a bifid uvula, a midline translucency called the “zona pellucida” and a palpable notch of the posterior hard palate.
Classifications of Clefts
Classification 3
Cleft Lip
Central—rare. In upper lip. Between two median nasal processes. (Hare lip)
Lateral—maxillary and median nasal process, commonest; can be unilateral or
bilateral
Incomplete cleft lip does not extend into nose
Complete cleft lip extends into nasal floor
Simple cleft lip is only cleft in the lip
Compound cleft lip is cleft lip with cleft of alveolus.
Classifications of Clefts
Classification 4
LAHS classification of cleft disorders
‘L’ for lip, ‘A’ for alveolus, ‘H’ for hard palate, ‘S’ for soft palate
Capital ‘LAHS’ for ‘complete type’
Small letters ‘lahs’ for ‘incomplete type’
Asterisks ‘lahs’ for microclefts
‘LAHSHAL’ for bilateral clefts
Complications of Clefts
Difficulty in sucking and swallowing. This is more commonly observed in cleft palate than in cleft lip.
Speech is defective especially in cleft palate, mainly to phonate B, D, K, P, T and G.
Altered dentition or supernumerary teeth.
Recurrent upper respiratory tract infection.
Respiratory obstruction (in Pierre-Robin syndrome)
Chronic otitis media, middle ear problems.
Cosmetic problems.
Hypoplasia of the maxilla.
Problems due to other associated disorders.
Treatment of Cleft Lip
Prior to Cleft Lip treatment, observe the:
Millard criteria
Millard Criteria
AKA Millard citeria (rule of 10)
10 pound in weight
10 weeks old
10 gm % haemoglobin
Treatment of Cleft Lip :
Millard cleft lip repair by rotating the local nasolabial flaps.
Management of associated primary or secondary cleft palate deformity.
Proper postoperative management like control of infection, training for sucking,
swallowing and speech.
Tenninson’s ‘Z’ plasty (Tenninson-Randall triangular flap).
Delaire timing of the cleft surgery – Unilateral/bilateral
cleft lip alone, in one stage operation done in 4–6
months.
For cleft palate alone involving only soft palate, in one stage, surgery is done in 6 months.
For cleft palate alone but involving both soft and hard palates—soft palate in 6 months; hard palate in 18 months.
In combined cleft lip and palate, unilateral or bilateral, in two stages—cleft lip and soft palate in 6 months; hard palate in 18 months
Cleft Palate: Etiology
It is due to failure of fusion of the two palatine processes.
Defect in fusion of lines between premaxilla (developed from median nasal process) and palatine processes of maxilla one on each side.
When premaxilla and both palatine processes do not fuse, it leads into complete cleft palate (Type I cleft palate).