|Year : 2016 | Volume
| Issue : 4 | Page : 566-568
Congenital bilateral syngnathia and tracheoesophageal fistula: A rare presentation
Ankit Khasgiwala1, Sagar Jangam2, Shashi Sharma3, Vilas Newaskar4
1 Department of Plastic and Reconstructive Surgery, Amandeep Hospital, Amritsar, Punjab, India
2 Department of Oral and Maxillofacial Surgery, Government Dental College, Aurangabad, Maharashtra, India
3 Department of Surgery, MGM Medical College and M Y Hospital, Indore, Madhya Pradesh, India
4 Department of Oral and Maxillofacial Surgery, Government College of Dentistry, Indore, Madhya Pradesh, India
|Date of Web Publication||15-Nov-2016|
Department of Plastic and Reconstructive Surgery, Amandeep Hospital, Amritsar, Punjab
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Congenital syngnathia (CS), first reported by Burket in 1936, is a rare condition, with <50 reported cases and is associated with other conditions and syndromes. CS restricts mouth opening, causing difficulty in feeding, swallowing, and respiration. This report puts forth the clinical findings and management of this challenging condition in association with tracheoesophageal fistula in a neonate.
Keywords: Aspiration pneumonitis, congenital, syngnathia, tracheoesophageal fistula
|How to cite this article:|
Khasgiwala A, Jangam S, Sharma S, Newaskar V. Congenital bilateral syngnathia and tracheoesophageal fistula: A rare presentation. Contemp Clin Dent 2016;7:566-8
| Introduction|| |
Congenital syngnathia (CS) is an unusual condition characterized by fusion of the jaw with inability to open the mouth at birth. Fusion can be unilateral or bilateral or complete and range from simple mucosal bands (synechiae) to complete bony fusion (synostosis). We present a case of a 2-day-old neonate with fusion of the maxillary and mandibular alveolar complex (Laster's Type 1b congenital maxillomandibular syngnathia) along with tracheoesophageal fistula (TEF) probably the first of its kind.
| Case Report|| |
A 2-day-old male neonate, preterm (36 weeks), normal delivery, weighing 2.0 kg, presented with a history of severely restricted mouth opening and frothing from mouth and nose and abdominal distention. The mother was healthy without any history of illness, trauma, or drug exposure. There was no history of consanguinity. The baby was the first child, and there was no incidence of similar kind of anomalies in close family members. Routine blood investigations were within normal limits.
The child had a slit-like space of 5–6 mm between the upper and lower arches in the region of the central incisors with rest of the alveolar areas showing fusion preventing detailed intraoral examination [Figure 1]. Radiological examination showed fusion of the upper and lower alveolar arches [Figure 2].
The patient was being given parenteral nutrition in view of reduced mouth opening and inability to pass infant feeding tube. The child had signs of aspiration pneumonitis (rattling respiration, cough, and cyanosis) and was rushed to emergency or to release the syngnathia under general anesthesia. A fiberoptic intubation through nasal route was performed using 2.2 mm ultrathin fiberoptic bronchoscope permitting passage of a 3.0 mm endotracheal tube (ETT). Bronchoscopy revealed a TEF Type C (Gross). The position of the ETT was verified and fixed subsequently. This finding correlated with clinical observation of frothing from mouth and nose at birth.
Syngnathia was released transorally; fusion on the left side was bony which was released by osteotome and mallet whereas scalpel blade was used to release the soft-tissue fusion on the right side. Mouth opening achieved after the release was 25 mm [Figure 3]. Hemostasis was attained, and a collagen membrane dressing was given to cover the raw area. Tongue, palate, and floor of the mouth were found to be anatomically normal after the release. No attempt at repair of TEF repair was done in this surgical appointment which was subsequently repaired after 48 h under general anesthesia. Unfortunately, the child developed septicemia likely due to previous aspiration pneumonitis and succumbed after 7 days.
| Discussion|| |
CS is a rare anomaly which presents as fusion of the jaws with inability to open the mouth at the time of birth. It can have varied presentations in maxillofacial complex ranging from simple fibrous union of alveolar ridges to bony fusion involving maxilla, mandible, temporomandibular joint, and even zygoma.
Laster et al. have classified CS based on site and extent of fusion and its association with other craniofacial anomalies [Table 1]., The case discussed previously had fusion of the upper and lower alveolus without any craniofacial anomaly, i.e., cleft, temporomandibular joint (TMJ) ankylosis, or other hence was classified under Laster's Type 1b congenital syngnathia., However, he had neck abnormality, i.e., cTEF. In our literature search (PubMed Central ® (PMC), and Google Scholar), we did not come across any case of CS associated with cTEF making this case a rare entity.
Various theories have been proposed to explain the etiology of this anomaly. These include:
- Persistence of buccopharyngeal membrane (Gorlin and Goldman)
- Oropharyngeal atresia secondary to persistence of buccopharyngeal membrane (Longacre)
- Amniotic constriction bands which lead to pressure in the region of the developing first branchial arch (Burket)
- Increasing period of contact between the alveoli due to the small jaw and decreased swallowing reflex (Walker and Frase, Humphrey),
- Antenatal exposure to drugs such as meclizine, large dose Vitamin A, which cause edema of the embryo and upsets skeletal growth (King, Kalter and Warkaney).,,
The differential diagnosis includes congenital TMJ ankylosis and glossopalatine ankylosis. Therefore, a careful clinical and radiological examination forms an essential part in diagnosing CS.
Treatment of congenital intermaxillary syngnathia is surgical release under general or local anesthesia depending on the site and extent of fusion. Intubation is facilitated by pediatric fiberoptic bronchoscope or elective tracheostomy. Blind nasal intubation is not preferred because of the risk of laryngeal edema and its sequelae. Alveolar fusion cases can be surgically approached through transoral route. However, fusion involving TMJ and zygomatic complex region requires extraoral approach. The use of interalveolar soft wedges has been recommended as a part of jaw physiotherapy to prevent the recurrence of the condition. Parental counseling and periodic recall to assess the craniofacial growth and possible recurrences form an essential part in the management of such anomaly.
| Conclusion|| |
A thorough literature search revealed that this is the first case of CS associated with TEF. There is no established treatment protocol for such anomaly considering the relative rarity of the condition. The management team should be aware of the wide range of severity of syngnathia along with other possible congenital deformities and adopt a treatment plan according to the situation and general condition of the patient. Furthermore, the parents must be counseled and informed about the surgical outcomes and associated comorbidities. Very little information is available on the long-term outcome of these patients.
We would like to thank Dr. Prathmesh Kapoor and Dr. Divashree Sharma for their valuable assistance and constructive suggestions for this article.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Broome M, Vial Y, Jacquemont S, Sergi C, Kamnasaran D, Giannoni E. Complete maxillo-mandibular syngnathia in a newborn with multiple congenital malformations. Pediatr Neonatol 2016;57:65-8.
Pinheiro PF, Simões e Silva AC, Pereira RM. Current knowledge on esophageal atresia. World J Gastroenterol 2012;18:3662-72.
Laster Z, Temkin D, Zarfin Y, Kushnir A. Complete bony fusion of the mandible to the zygomatic complex and maxillary tuberosity: Case report and review. Int J Oral Maxillofac Surg 2001;30:75-9.
Fallahi HR, Naeini M, Mahmoudi M, Javaherforoosh F. Congenital zygomatico-maxillo-mandibular fusion: A brief case report and review of literature. Int J Oral Maxillofac Surg 2010;39:930-3.
Gorlin RJ. Developmental anomalies of the face and oral structures. In: Gorlin RJ, Goldman HM, editors. Thoma's Oral Pathology. 6th
ed. St. Louis: The C.V. Mosby Company; 1970.
Longacre JJ. Congenital atresia of the oropharynx. Plast Reconstr Surg 1951;8:341-8.
Burket LW. Congenital bony temporomandibular ankylosis and facial hemiatrophy. J Am Med Assoc 1936;106:1719.
Walker BE, Fraser FC. Closure of secondary palate in three strains of mice. J Embryol Exp Morphol 1956;4:176.
Humphrey T. The relation between human fetal mouth opening reflexes and closure of the palate. Am J Anat 1969;125:317-44.
King CT. Teratogenic effects of meclizine hydrochloride on the rat. Science 1963;141:353-5.
Kalter H, Warkany J. Experimental production of congenital malformations in strains of inbred mice by maternal treatment with hypervitaminosis A. Am J Pathol 1961;38:1-21.
Rao S, Oak S, Wagh M, Kulkarni B. Congenital midline palatomandibular bony fusion with a mandibular cleft and a bifid tongue. Br J Plast Surg 1997;50:139-41.
Seraj MA, Yousif M, Channa AB. Anaesthetic management of congenital fusion of the jaws in a neonate. Anaesthesia 1984;39:695-8.
[Figure 1], [Figure 2], [Figure 3]