Tagliarini José V, Nakajima Victor, Castilho Emanuel C
Department of Ophthalmology, Otorhinolaryngology and Head and Neck Surgery, Medical School, UNESP.
Braz J Otorhinolaryngol. 2005 Mar-Apr;71(2):246-9. doi: 10.1016/s1808-8694(15)31319-7. Epub 2005 Aug 2.
The congenital stenosis of pyriform aperture is an unusual cause of neonatal nasal obstruction. It is due to bony overgrowth of the nasal lateral process of the maxilla. Initially this narrowest part of nasal airway was considered an isolated deformity; subsequently the congenital Stenosis of pyriform aperture was thought to represent a microform of holoprosencephaly. In this report a male neonate had respiratory distress, cyclic cyanosis and apnea after delivery. The patient underwent surgical correction of pyriform stenosis by sublabial access. In the follow up, the patient had good evolution. The report of this deformity shows an important cause of neonatal nasal obstruction and its differential diagnosis with bilateral choanal atresia. Congenital stenosis of nasal pyriform aperture can be surgically corrected when necessary.
梨状孔先天性狭窄是新生儿鼻阻塞的一种罕见原因。它是由于上颌骨鼻侧突的骨质过度生长所致。最初,鼻气道的这个最狭窄部分被认为是一种孤立的畸形;随后,梨状孔先天性狭窄被认为是全前脑畸形的一种微小型。在本报告中,一名男婴出生后出现呼吸窘迫、周期性紫绀和呼吸暂停。该患者通过唇下入路接受了梨状孔狭窄的手术矫正。在随访中,患者恢复良好。对这种畸形的报告显示了新生儿鼻阻塞的一个重要原因及其与双侧后鼻孔闭锁的鉴别诊断。必要时,梨状孔先天性狭窄可通过手术矫正。