Related Experiment Video
Updated: Sep 27, 2026

Endoscopic Septoplasty with Limited Two-line Resection: Minimally Invasive Surgery for Septal Deviation
Published on: June 20, 2018
[Nasal congenital cysts and fistulas: clinical and surgical aspects]
M A Vendrell1, R Carrasco Torrents, F J Parri Ferrandis
1Servicio de Cirugía Pediátrica, Hospital Sant Joan de Dèu, Po Sant Joan de Dèu 2, 08950 Esplugues, Barcelona.
Abstract:
Eight patients affected with cysts or fistulae on the midline at the nose bridge (back of the nose) have been treated at the Pediatric Surgery Service of the Hospital Sant Joan de Dèu in Barcelona from march 1995 to october 1996. Six patients had a cystic mass (four of them having an intranasal prolongation) and two had a fistulous orifice (one of them also having intranasal prolongation). The test with the highest diagnostic sensibility was the CT-scan, which showed a bifid crista galli and intranasal prolongation in 5 of the patients. Pathologic exam confirmed the diagnosis of dermoid cyst. At follow-up, all patients were doing well. Congenital cysts and fistulae at the nose bridge (back of the nose) may appear as a trivial condition; the possibility of them being the only clinical feature of an intranasal or intracranial prolongation is the reason for a deeper study in order to determine the extension of the lesion. The treatment is always surgical removal of the cyst and the fistulous pathway at the time of diagnosis, regardless of the patient's age, thus avoiding possible infectious complications.
Related Concept Videos
Nose and Nasal Cavity
Cranial Bones: Lateral View
The temporal bone forms the lower lateral side of the skull. The temporal bone is subdivided into several regions. The flattened upper portion is the squamous portion of the temporal bone. Below this area and projecting anteriorly is the zygomatic process of the temporal bone, which forms the posterior portion of the zygomatic arch. Posteriorly is the mastoid portion of the temporal bone. Projecting...
Suctioning the Nasopharyngeal Airway
Equipment Required
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...
Epistaxis
Etiology
Possible causes of this condition include high blood pressure, trauma, low humidity, upper respiratory tract infections, allergies, foreign bodies, nasal inhalation of corticosteroids or illicit drugs, excessive use of decongestant nasal sprays, facial or nasal surgery, anatomic malformation, tumors, or systemic...
