Hoffer M E, Tom L W, Wetmore R F, Handler S D, Potsic W P
Division of Otolaryngology, Children's Hospital of Philadelphia, Pa.
Arch Otolaryngol Head Neck Surg. 1994 Apr;120(4):449-53. doi: 10.1001/archotol.1994.01880280077015.
Congenital tracheal stenosis is a rare congenital anomaly, with less than 70 reported cases in the literature. The presenting signs and symptoms of stridor, recurrent pneumonia, and respiratory distress are commonly seen in other conditions. The rarity of congenital tracheal stenosis and the diverse presentations make accurate early diagnosis difficult and frequently lead to inappropriate treatment. We treated three patients with congenital tracheal stenosis who presented with different sites of stenosis. Each patient displayed different symptoms and required individualized management. The treatment of congenital tracheal stenosis depends on identifying the site and extent of the stenosis. We reviewed the embryogenesis and treatment of this abnormality and developed a new classification system that will aid in the management of congenital tracheal stenosis.
先天性气管狭窄是一种罕见的先天性异常,文献报道的病例不足70例。喘鸣、反复肺炎和呼吸窘迫等临床表现常见于其他病症。先天性气管狭窄的罕见性以及多样的表现使得早期准确诊断困难,常常导致治疗不当。我们治疗了3例先天性气管狭窄患者,他们的狭窄部位各不相同。每位患者表现出不同的症状,需要个体化管理。先天性气管狭窄的治疗取决于确定狭窄的部位和范围。我们回顾了这种异常的胚胎发生和治疗方法,并制定了一种新的分类系统,这将有助于先天性气管狭窄的管理。