- Case report
- Open Access
- Open Peer Review
Bilateral congenital choanal atresia and osteoma of ethmoid sinus with supernumerary nostril: a case report and review of the literature
© Li et al; licensee BioMed Central Ltd. 2011
- Received: 13 April 2011
- Accepted: 20 December 2011
- Published: 20 December 2011
Congenital choanal atresia is a relatively rare deformity, especially bilateral congenital choanal atresia. We report a case of bilateral congenital choanal atresia in a 22-year-old Chinese man, who was also diagnosed with congenital right accessory nasal deformity, osteoma of his left ethmoid sinus and congenital keratoleukoma of his right eye.
A 22-year-old Chinese man presented with mouth breathing, sleep snoring and difficult feeding after birth, with no olfactory sensation. Three-dimensional computed tomography revealed bilateral choanal atresia and a high density bony shadow in his left ethmoid sinus that extended to his left frontal sinus.
Choanal atresia is often accompanied by other congenital abnormalities. To the best of our knowledge, this is the first report of choanal atresia accompanied by congenital accessory nasal deformity and congenital keratoleukoma.
- Corneal Opacity
- Ethmoid Sinus
- Choanal Atresia
- Mouth Breathing
- Charge Syndrome
Choanal atresia was first reported by Johann Roderer in 1755 . Its incidence is about 8.2 per 100, 000  and the primary symptoms, such as bilateral imperforation, dyspnea and inability to suck after birth, are attributed to postnatal nasal obstruction. In serious cases, ensuing suffocation can lead to death. We present a rare case of bilateral congenital choanal atresia, which was accompanied by congenital right accessory nasal deformity, osteoma of his ethmoid sinus, and congenital keratoleukoma of his right eye.
A 22-year-old Chinese man presented with mouth breathing, sleep snoring, and loss of olfactory sensation. Difficult feeding after birth was reported, without dyspnea or asphysia. He had no relevant family history.
Congenital accessory nasal deformity is a supernumerary malformation in the external nose. Supernumerary malformation may appear in different ways. It may replace the normal structure or co-exist with it. Removal of the congenital accessory is the optimal treatment method. Tambwekar  reported one similar case. The patient in our report bore three anterior nares, however, this should be differentiated from three-nostril malformation, a type of cleft nose occurring when the median line of the nasal ridge presents as a major groove, or the mesenchymal tissue between two olfactory saccus fails to evolve into a thin but firm septal cartilage in the embryonic period, resulting in the nasal dorsum broadening and the cleft emerging. In our case, only the soft tissue formed the malformation in one side of the anterior nares, therefore this case was diagnosed as 'congenital accessory nasal deformity'.
Congenital atresia of the posterior nares can be categorized into two types: unilateral (60%) and bilateral (40%) atresia . According to the closure tissue, it can be subdivided into membranous, bony or mixed bony-membranous atresia . Although the incidence of congenital atresia of posterior nares is low, other congenital abnormalities often coexist . In the case of our patient, congenital keratoleukoma of the right eye was an accompanying abnormality. Burrow et al.  stated that 26.4% of the choanal atresia they found was isolated, while 73.6% was associated with other anomalies. CHARGE syndrome may manifest with choanal atresia . However, according to Verloes , our patient cannot be diagnosed as having CHARGE syndrome. Congenital bilateral atresia of the posterior nares is a very dangerous disease which can cause death in infants because the inability to nose breathe will lead to tremendous difficulty in sucking and feeding. Mouth breathing in the long term may result in malformation in the midface and/or the hard palate . A high-arched palate was observed in our patient. In light of Brown's classification , our patient was diagnosed as having membranous congenital bilateral choanal atresia.
Osteoma is one common benign tumor which grows slowly in nasal sinuses. In most cases, patients do not suffer from any clinical symptoms; osteoma is found in imaging studies by accident. In general, osteoma of the paranasal sinuses occurs in the frontoethmoid region. The etiology is still unknown; however, there are three different hypothesis available suggesting that embryologic, traumatic or infective factors are involved . The incidence of osteoma is 62% in the frontal sinus, 24% in the ethmoid sinus, and rarely in maxillary and sphenoid sinus . An osteoma in nasal sinuses can be subcategorized into three basic histological types: compact, cancellous or mixed . Imaging studies, especially CT and three-dimensional CT scans, are often applied for diagnoses . If the osteoma does cause some discomfort, resection is recommended. The surgical approach depends on the location and size of the tumor. A small osteoma in the ethmoid sinus can be removed under nasal endoscope. For a large osteoma, lateral rhinotomy is preferred. When an osteoma infiltrates the front cranial basalis, a combined craniofacial approach is usually considered .
Keratoleukoma is a thin, opaque, abnormal coating on the cornea of the eye. It is one kind of corneal opacity. According to the thickness of the coating, a corneal opacity is graded into corneal nebula, corneal macula and keratoleukoma. The most common causes of corneal opacity are ocular trauma (50.6%), retinal disease (15.5%), measles (9.5%) and congenital etiologies (5.5%) . Corneal opacities vary greatly in extent and location and are usually associated with other anomalies , for example the bilateral congenital choanal atresia and congenital right accessory nasal deformity in our patient. Because corneal opacity is a cause of blindness , timely treatment is crucial. A study has shown that 64.92% of patients underwent cosmetic treatment after the primary visit . Corneal transplantation should be performed when needed .
Congenital bilateral choanal atresia is a life-threatening disease in newborns. However, it can also be found in adults, who may present with mouth breathing, sleep snoring and symptoms of nasal obstruction. Choanal atresia is often accompanied by other congenital abnormalities. In this case report we demonstrate the importance of clinical awareness and of general medical examination when encountering similar patients.
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.
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