Bilateral congenital alveolar synechiae—a rare cause of trismus
© Panda et al. 2016
Received: 9 January 2016
Accepted: 15 February 2016
Published: 19 February 2016
Congenital alveolar synechiae is a rare anomaly mostly presenting in association with cleft palate. Owing to reduced mouth opening, feeding difficulties, and compromised airway in extreme cases along with presentation in early neonatal period, these patients present unique challenges to the surgeon as well as the anesthetist. Here, we discuss the surgical and anesthetic management of this entity in a 12-month-old female child.
Bilateral congenital alveolar synechiae is a rare clinical entity frequently described in association with other craniofacial anomalies . This condition is recognized in the early neonatal period due to feeding difficulties, restricted mouth opening, and in extreme cases, presenting with respiratory distress. Early surgical intervention is therefore warranted to address the neonates’ nutritional needs and optimal growth. The surgical, anesthetic, and airway challenges that these patients present with have been reviewed in this case report.
A 1-year-old female was referred to our department with complaints of decreased mouth opening since birth. The child was born out of a non-consanguineous marriage. The mother had a full-term vaginal delivery. Birth weight was 2.5 kg. Apgar scores were unknown. The perinatal period was uneventful. The clinician attending the child, however, made note of the reduced mouth opening and the presence of bands adhering the upper and lower alveolus. Family history was also not contributory. The child attained age appropriate milestones and had no other systemic manifestations. The patient had no feeding or breathing difficulties and sought medical help for reduced mouth opening at the age of 12 months.
On examination, there were no dysmorphic features. Cardiovascular and neurological assessments were normal. No other musculoskeletal anomalies were found. Detailed oral cavity examination could not be performed due to trismus. Evaluation of oral cavity was performed with a nasal endoscope and two fibrous bands could be identified between upper and lower alveolus of thickness of 3 to 4 mm approximately, about 3 mm from the oral commissure on the left and 5 mm from the commissure on the right (Fig 1). The patient also had a concomitant bifid uvula. Bony ankylosis of temporomandibular joint was ruled out on computed tomography.
Patient had an uneventful postoperative recovery. Oral feeds were initiated immediately after recovery from anesthesia and was tolerated well by the patient.
Congenital intraoral synechiae is a rare congenital anomaly with approximately 60 cases documented in the literature . It rarely presents in isolation. Of the 50 cases reported by Gartlan , only seven patients presented with isolated alveolar fusion. Associated anomalies include Van der Woude syndrome, popliteal pterygium syndrome, and orofacial digital syndrome . The most common association is with cleft palate (cleft palate lateral synechiae syndrome) [1, 3].
These patients present in the early neonatal period due to restriction of mouth opening interfering with feeding and airway [1, 2, 4]. Our patient, however, presented late due to absence of gross craniofacial anomalies, absence of severe trismus owing to posterior location of the bands. Bifid uvula was the only concomitant anomaly found.
Various theories have been put forth to explain the association between cleft palate and intraoral synechiae. The most convincing is the sequence of cleft palate predisposing to increased mucosal contact between tongue and developing alveolus . Other possible mechanisms like persistence of buccopharyngeal membrane and local ischemia of amniotic bands causing pressure on the first branchial arch also explain the rare occurrence of isolated alveolar synechiae. Airway management presents unique challenges to the anesthesia team. Blind nasal intubation was attempted in the past . Tracheostomy is, generally, reserved as a last resort in these patients with only one article quoting the need for tracheostomy in a 38-week-old male infant presenting with marked desaturations . Nasotracheal intubation with flexible fiberoptic bronchoscope as performed in our case is considered the gold standard [1, 5].
Treatment consists of dividing the bands as early as the child’s general condition permits to optimize feeding, craniofacial development, and prevent fibrous ankylosis due to disuse. Diode laser has been used in our patient to minimize blood loss, post operative pain, prevent collateral damage, and hence hasten the healing process and prevent reformation of the adhesions.
Trismus in a neonate presents unique challenges to the treating physician for airway and feeding management. Timely referral to oral and maxillofacial center with good anesthetic expertise can circumvent the problems of failure to thrive and poor development. Flexible fiberoptic intubation can avoid the additional morbidity caused by tracheostomy in such young infants. The use of diode laser not only reduced surgical time but also played a significant role in expediting healing process and helped in early initiation of oral feeds.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
The authors thank the participant for the informed consent to share the results of this procedure. SP thanks Shradha Panda and Praveen Dhanalakota for their excellent processing of clinical photography.
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