What is Hemifacial Microsomia?

By Pravin K. Patel, MD and Bruce S. Bauer,

MD Children’s Memorial Hospital, Chicago, IL

 

Early in the child’s embryonic development the structures destined to become the various parts of the face may not develop normally.  The left and right side of the face may not grow equally or the entire lower jaw may not keep pace with the rest of the developing face.  Not uncommonly these deformities of the jaw are also associated with the underdevelopment of the ear and other soft tissues, the overlying facial muscles and skin of the face.
 
The term Hemifacial or Craniofacial Microsomia is used to describe the condition when one side of the child’s face is smaller and malformed and the term microtia (micro means small and otia means ear) is used.  The term Goldenhar Syndrome may be used to describe this group of deformities when the eye (epibulbar dermoids) and spine (hemivertebra) are also affected.  There is a broad spectrum to this condition and there are many names associated with it:  Tessier Number 7 cleft, oral-mandibular – auricular syndrome, first and second branchial arch syndrome, lateral facial dysplasia, and others.  Although it is described as involving only one side (unilateral condition) of the face, it may also involve both sides (bilateral) of the face to different extent resulting in an asymmetrical bilateral hemifacial microsomia.
 How common is it and How or Why does it occur?
 At most craniofacial centers, the second most common deformity seen, after children with cleft lip and palatal deformities, is hemifacial Microsomia.  It is said to occur in approximately 1 in 3500 to 1 in 5000 births.  For families with one child affected with hemifacial microsomia, the likelihood of a second child with the same condition is less than 1%, and the risk is 3% for an adult with hemifacial microsomia to pass this on to his  children.  There are some variants of hemifacial microsomia where the likelihood of passing this to their children  is significantly greater and a discussion with a geneticist is valuable.
 
A genetic cause has not yet been identified and it is believed that most cases occur because of an event in the developing embryo that disrupts the normal development of the ear and jaw.  In the first six weeks of embryonic life, the ear forms from the coalescence of six small bumps, and closely associated with the formation of the ear is the development of the lower jaw.  Because of this close relationship, ear deformities are frequently associated with deformities of the lower jaw, the mandible.  While how it may occur can be understood, exactly why it occurs remains unknown today.
 What are the anatomic and functional deformities?
 Each of the structures is involved to varying degrees of severity.  In some children only the ear deformity is  evident while in others the ear is normal but the jaw is affected.  In most severe cases, all the soft tissue and  bony structures are hypoplastic.
 
The Soft Tissue Deformity
The extent of soft tissue involvement may vary from the barely perceptible to severe deficiency.  The structures affected include the skin, the muscles and nerve of facial expression, the salivary gland and the ear.
 
It is the appearance of an abnormal external ear that is the most noticeable feature.  Frequently it is no more than  a ‘lump’ on the side of the face and bears little resemblance to the structure we recognize as an ear.  Along with  the external ear deformity, the ear canal and the internal structures of the ear that allow for hearing may also be affected.  While children with unilateral involvement have problems locating the direction from which sound
comes, most children do not need hearing aides as long as the unaffected ear has normal hearing.  In some children the various branches of the facial nerve and the associated muscles which allow for facial expression may be affected.  Various degrees of facial paralysis are seen.  The muscles that work the lower jay and allow mastication are also affected and occasionally the muscles of the soft palate and tongue on the same side as well.  The thickness of the skin and underlying tissue is deficient of hypoplastic.  In some children there is a lateral cleft of the lip extending from the corner of the mouth toward the ear resulting in macrostomia, an enlarged opening of the mouth.
 
The Bony Deformity
Even though the upper facial bones (maxilla, zygoma, orbit and temporal bones) may be involved, it is the lower jaw, the mandible that is believed to be the “keystone” to this deformity.  With continued asymmetrical growth  of the mandible, the facial deformity worsens.  The amount of deficiency (hypoplasia) of the mandible varies from being minimally involved to where there is complete absence of the vertical portion (ramus) and the  various bony structures (zygomatic arch and condyle) of the temporomandibular joint.  The chin is deviated to  the involved side and becomes more noticeable with opening and closing of the mouth.  This hypoplasia of the mandible affects the normal downward growth of the upper jaw, the maxilla, and this results in a cant to the  teeth.  In addition, the cheek bone (zygoma) may be deficient and the orbit may be malpositioned.  


How is it treated?
These varied deformities require treatment in order to improve a child’s ability to breathe, eat, speak, and hear.  Because of the degree and the complexity of various structures involved, a coordinated approach is needed to reconstruct anatomically and functionally the individual elements if the face.  Caring for children with  hemifacial microsomia requires a multidisciplinary approach.  This means a close co-operation of a number of pediatric specialists – plastic surgeons, otolaryngologists, dentists, orthodontists, audiologists, speech and  language pathologists, geneticist.  Because of the great variability of presentation, treatment will necessarily  vary and must be individualized.  Nevertheless, the goals remain the same:  to restore the normal shape and  contour of the face by both correcting the bony deformity and the external ear and the soft tissue deficiency and  the external ear and to restore the normal function of hearing, speech and bite to the extent possible.
 
The key to reconstructing the facial skeletal deformity is correcting the cant of the mandibular asymmetry.   While in some cases orthodontic devices can sometimes be used to stimulate mandibular growth, more often when the deformity is significant surgical procedures are needed.  This means surgically repositioning the lower jaw to correct the cant and bring the chin to the center to a more symmetrical position to match the other side. On the side with the bony deficiency, the mandible can be lengthened by using a rib or by using a newer technique called distraction osteogenesis that gradually lengthens the bone by using a special device.  Distraction osteogenesis may provide a means of treating many of these deformities both at an earlier age and with the  potential for better long-term results than conventional treatment of using a rib graft typically done in early  childhood.  When the mandible is lowered, this creates what is called an “open bite”, since the upper jaw remains in its uncorrected canted position, the teeth of the upper jaw do not meet the teeth of the lower jaw on  the affected side.  The upper jaw is then gradually brought down to meet the lower jaw.  Even with correction of  the occlusal cant in childhood, both upper and lower jaw may need to be simultaneously repositioned in adolescence at a time when facial growth is completed.  This requires cutting the bones of the upper and lower jaw, realigning the various elements of the facial bones and fixing them into their position with plates and screws.
 
Reconstructing the ear is a surgical challenge.  The ear is built from the child’s own rib cartilage and requires a  number of stages, frequently three to four operations.  Reconstruction of the ear typically begins between ages 5 and 6 when most of the growth if the normal ear on the other side is nearly complete and the child’s chest wall cartilage is large enough to sculpt the ear framework.  The size and position of the normal ear is used as a template for the new ear.
 
The ear framework is placed in either a skin pocket buried under a thin layer of vascularized tissue from the  scalp and then covered with a skin graft.  The lobule remnant frequently present is repositioned more symmetrically and the tragus is constructed from the concha or the bowl of the other ear.  Each of these may be either a separate surgery or integrated with other surgical procedures.  Both the ear reconstruction and jaw reconstruction can frequently be integrated in childhood.
 
Even after re-alignment of the facial skeleton there is not infrequently a soft tissue deficit.  This requires transplanting a soft tissue from another part of the body to restore the symmetry in volume.  Frequently the skin from the upper back (scapular region) is used.  In order for this tissue to live, the small vessels measuring between 1 to 2 mm in size must be connected to the vessels in the face.  This is done using a microscope and is called microvascular surgery.

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