Hemifacial microsomia (HFM), also known as unilateral otomandibular dysostosis or lateral facial dysplasia, is an asymmetrical, congenital malformation of the 1st and 2nd branchial arches and the second most common craniofacial anomaly after cleft lip and palate. Patients present with unilateral hypoplasia of the ear, facial skeleton (maxilla, mandibular, zygoma, and temporal bones), and surrounding soft tissue. HFM and Goldenhar syndrome are considered variants under the same clinical continuum of disorders termed the oculoauriculovertebral spectrum (OAVS), with Goldenhar syndrome encompassing HFM phenotypes along with epibulbar dermoid and vertebral anomalies.
HFM is a dysfunction of the 1st and 2nd branchial arches, which are formed by the neural crest cells (NCC). The cause of HFM is uncertain, but two leading theories are vascular injury of the stapedial artery and anomalous migration of the neural crest cells. The heterogenous phenotypical appearance of HFM has been theorized to be caused by a combination of genetic and environmental factors that disrupt the vascularization and development of the first and second pharyngeal arches, which form during the first 4 weeks of pregnancy.
Embryonically, the first branchial arch becomes the maxilla, mandible, zygoma, muscles of mastication, trigeminal nerve, anterior auricle (tragus, helical root, helix), malleolus, and incus. The second branchial arch becomes the hyoid bone, muscles of facial expression, facial nerve, stapes, and the remainder of the auricle (antihelix, antitragus, and lobule). Disruption during pharyngeal arch development from genetic defects, teratogens, smoking, hormonal therapy, vascular injury, vasoactive medications, cocaine, and maternal-fetal factors such as maternal diabetes, hypothyroidism, and celiac disease can result in hypoplasia or aplasia. Genetic mutations and chromosomal abnormalities that are associated with HFM include trisomy 10p, 12p13.33 microdeletion, 22q11.2 microdeletion, large 5p deletion, and 10.7 cM on chromosome 14q32.
HFM is the second most common congenital craniofacial defect after cleft lip and palate. Most cases are sporadic, with some studies suggesting both autosomal dominant and recessive inheritance patterns with incomplete penetrance. The incidence rate is estimated to range from 1 in 3500 to 1 in 5600 live births in the United States. Certain studies have reported a 3 to 2 male predominance with the majority of patients presenting with right-sided defects, while others have indicated no significant differences in gender or laterality. There is a 10% chance of bilateral presentation, most commonly in cases of autosomal dominant inheritance.
There are three interrelated pathogenic models for the development of HFM. No model is completely concordant with the varying presentation of HFM. Distinct phenotypes of HFM may be caused by different factors influencing separate pathogenic models.
HFM can present with a spectrum of deformities involving the eyes, ears, and the first two pharyngeal arches. Ocular deformities include strabismus, anophthalmia, microphthalmia, eye asymmetry, cleft eyelid, and exophthalmia. Auricular abnormalities include preauricular appendage, preauricular fistula, microtia, ear asymmetry, and external auditory canal atresia. Deformities of the first and second pharyngeal arches include cleft lip and palate, bifid tongue, mandibular hypoplasia, maxillary hypoplasia, oral malocclusion, and dental malformations.
Although the term HFM implies facial involvement only, patients with HFM often have associated extracranial defects. Neurological abnormalities range from 5% to 15%, cardiac in 14% to 47%, genitourinary in 5% to 6%, pulmonary and gastrointestinal in 10%, and skeletal malformations in up to 40% to 60%.
Children presenting with HFM should have a detailed, three-generation family history conducted to identify any malformations that are characteristic for HFM. A comprehensive prenatal and birth history should be obtained to identify any maternal-fetal factors such as gestational diabetes, maternal hypothyroidism, and any medications or drug use during pregnancy. Parents should be asked if the child has any obstructive sleep symptoms, difficulties with swallowing and feeding, and speech development.
The physical exam should focus on identifying facial abnormalities and asymmetries involving the auricle, ossicles, zygoma, maxilla, mandible, jaw mobility, and occlusion. Cleft lip and palate are common in HFM patients and should be evaluated. Ophthalmologic findings such as ocular dermoid cysts and vertebral abnormalities such as scoliosis may indicate the more severe variant of Goldenhar syndrome.
The minimal diagnostic criteria for HFM requires either 1) Ipsilateral mandible AND auricle defects or 2) Asymmetric mandible OR auricle defects with the involvement of 2 or more indirectly associated anomalies OR a positive familial history of HFM.
The posteroanterior cephalogram is the gold standard for assessing facial asymmetry. Measurements such as the midline deviation of maxilla and mandible, ramus height, and occlusal cant are taken for surgical planning. Photography is used to document facial appearance throughout the treatment process. Other imaging modalities such as computerized tomography (CT) have been utilized to assess ossicles, middle ear cavity, and facial bone size and shape for preoperative planning. 3D facial skeleton models can be created from CT scans to help guide surgical device placement.
Many patients with HFM have airway and feeding difficulties due to underdevelopment of the pharynx, larynx, esophagus, mandible, and mastication muscles. Obstructive sleep apnea, swallowing difficulty, and cleft lip and palate were diagnosed in 17.6%, 13.5%, and 15.9% of patients with craniofacial malformations, respectively. Thus, HFM patients, especially those with micrognathia and OSA symptoms, should undergo polysomnography and swallow evaluation by a speech-language pathologist.
Additional screenings include an audiogram to assess for hearing loss, perceptual speech analysis for speech development, and psychosocial assessment. Cervical spine radiographs for vertebral defects and renal ultrasound for noncraniofacial malformations should also be performed. Chromosomal analysis and genetic counseling can also be offered for families with suspected genetic inheritance.
Given the heterogeneous presentation of HFM, an individualized and interprofessional approach is necessary. Functional impairments such as airway obstruction and dysphagia should be addressed first. HFM patients often have a narrow oropharyngeal airway and nasal obstruction from midface and mandibular hypoplasia. Airway complications can include difficult intubation, obstructive sleep apnea, and respiratory distress. Tracheotomy is the standard treatment for those with severe airway obstruction. Although neonatal distraction osteogenesis has been described, its effectiveness is lower in patients with craniofacial malformations compared to those with Pierre-Robin sequence, due to the absence of catch up growth. Growing infants with dysphagia may also require a gastrostomy tube for nutrition.
Reconstructive surgery for HFM has the goal of improving facial symmetry, jaw function, and normal occlusion. The type of surgery performed is based on the severity of the defects.
Hemifacial microsomia can present with a heterogenous array of facial defects with different levels of severity. Many disorders involving facial anomalies can be misdiagnosed as hemifacial microsomia including:
The timing of reconstructive surgical intervention is controversial. Proponents of early intervention hypothesize that mandibular asymmetry worsens over time as the affected side undergoes minimal growth, resulting in secondary deformities. They propose that early intervention can improve growth potential, masticatory function, dental development, and patient self-confidence.
Supporters of delayed surgical intervention recommend correction upon skeletal and dental maturity (age 15 in boys and 13 to 15 in girls) to avoid relapse of asymmetry and need for additional surgery as well as decreased blood loss and improved patient compliance. Large systematic reviews have concluded no evidence in supporting early surgical reconstruction and recommend postponing surgery until completion of dental and bony growth.
The timeline for treatment depends on the patient's age and severity of malformations. During infancy, indicated interventions include correction of cleft lip and palate, hearing aids for hearing loss, osteotomies for significant orbital dystopia and plagiocephaly, and mandible distraction for patients with severe retrognathia resulting in respiratory or feeding difficulties. During the skeletal growth phase from ages 6 to 12, reconstruction of the malformed auricle or placement of a prosthesis is recommended.
Maxilla and mandible defects can be addressed with orthodontic devices. Costochondral grafts or mandibular distraction can also be considered. In adolescence and adulthood, definitive reconstruction surgery of the facial skeleton to improve facial asymmetry and occlusion is recommended along with soft tissue augmentation using free tissue transfer or fat grafting. Any revision surgeries can also be done at this time.
Due to the wide variable presentation of HRM, several classification systems have been proposed to better differentiate the phenotypical presentation to help improve diagnosis, treatment, and prognostic data. The first classification proposed by Pruzansky in 1969 focused on the characteristics of the mandible and glenoid fossa. In 1987, David et al. proposed the SAT (skeletal malformations, auricular involvement, and soft tissue defects) system, which was further expanded by Vento et al. to become the OMENS (orbit, mandible, ear, nerve, soft tissue) classification. Finally, the OMENS plus was developed by Tuin et al. to incorporate abnormalities of noncraniofacial structures.
Studies have indicated that mandibular distraction osteogenesis with internal devices is effective in lengthening the mandible and improving facial symmetry, appearance, and dental occlusion on postoperative cephalograms and radiographs. However, few studies exist on long-term outcomes. Hollier et al. followed patients for 12 to 92 months and found a recurrence rate of 51% to 100% within 42 to 92 months.
Similar studies have also shown similar rates of recurrence requiring revision surgery. This highlights the importance of following patients until skeletal and dental maturity. In a 2012 study by Mezzini et al. showed that the asymmetrical facial proportions and growth patterns of HFM patients are genetically influenced and revert back to the original asymmetry even after mandibular distraction. Patients and families should be counseled on the high likelihood of revision surgery throughout childhood and adolescence.
Mandible distraction osteogenesis is the preferred method of treatment for HFM patients but can present with challenges and complications. A systemic review by Verlinden et al. found a complication rate of 43.9%, with 13.9% requiring revision surgery, hospitalization, or resulting in permanent sequelae. Nerve injury to the inferior alveolar nerve or mental nerve ranged from 4.2% to 37.5%.
Mucosal and soft tissue dehiscence were seen in 1.6% to 3.1% due to the thin soft tissue overlying the hypoplastic bone. Lingual displacement from the traction of the mylohyoid muscle by the osteotomized segment is reported in 7.6% of cases. Misalignment of the mandible occurred in 0.6% of cases. Mandible fracture was seen in 2.8%. Other complications include bony non-union, insufficient bone formation, hardware exposure, facial scarring, wound infection, and mandibular necrosis.
After the surgical placement of internal distractors, the patients are admitted for airway observation. Patients are discharged once able to breathe without issues and are tolerating an adequate diet. After a latency period of 4-7 days for school-aged children, the distraction is activated at a rate of 1 mm per day until the desired length based on preoperative design. Parents are taught how to turn the distractor and keep the surgical site clean at home.
Once distraction is completed, the externally exposed rods are removed close to the skin. After 2 to 3 months of bony consolidation, the patient is brought back to the operating room to remove the internal device. A series of cephalograms are taken at the beginning of activation, end of activation, prior to device removal, and 1 year postoperatively.
Hemifacial microsomia may result from aberrant neurological regeneration impacting the salivary glands and integumentary system. Diagnosis and management should consist of an interprofessional team, including an otolaryngologist, plastic reconstructive surgeon, oral maxillofacial surgeon, ophthalmologist, primary clinician, psychologist, and geneticist.
Patient and family education on hemifacial microsomia can be challenging due to the heterogeneous presentation and the need for interprofessional management. Early involvement of a speech-language pathologist to address any functional deficits in speech and swallow is crucial. Introduction to a genetic counselor can be beneficial to address genetic and chromosomal abnormalities in the family. Patients and their families should be educated on the different treatment options and the timeline for reconstructive surgery. Studies have shown that the recurrence of asymmetrical bony growth is common after primary surgical management. Delay of surgical intervention until skeletal and dental maturity is often the best option to prevent revision surgery.
However, prolonged visible and functional impairments may have a significant impact on psychosocial development and personality formation in children. Patients and parents should be counseled on the pros and cons of earlier surgical intervention to obtain a more normal childhood with the caveat of future revision surgery versus delayed surgical intervention.
Patients with hemifacial microsomia should be managed by an interprofessional team of otolaryngologists, plastic surgeons, oral maxillofacial surgeons, ophthalmologists, audiologists, speech-language pathologists, primary clinicians, psychologists, and geneticists. Children born with hypoplastic facial defects should be thoroughly evaluated by primary clinicians and geneticists for prompt diagnosis and referral to the reconstructive surgeons.
Other craniofacial microsomia syndromes with similar presentations should also be considered to determine if there are any accompanying vertebral or internal organ malformations. Studies have shown that reconstruction is best performed once children reach skeletal and dental maturity. As patients with HFM often require multiple surgeries throughout childhood and adolescence, they must be closely monitored by their primary clinician and reconstructive surgeons for both immediate and long-term functional and aesthetic outcomes. Finally, patients may develop social and functional impairment due to their condition.
Referral to a speech-language pathologist for speech and swallow, as well as psychosocial support, is recommended. Formal peer support groups with similar craniofacial malformation diagnoses can aid patients and parents in addressing their concerns.
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