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先天性气道异常。

Congenital airway anomalies.

机构信息

Program Director Pediatric Airway Unit, Mackenna Children's Hospital, University of Chile, Clínica Las Condes Medical Center. Santiago, Chile.

Pediatric ENT, Hospital De Clinicas de Porto Alegre, Porto Alegre, Brazil.

出版信息

Semin Pediatr Surg. 2021 Jun;30(3):151055. doi: 10.1016/j.sempedsurg.2021.151055. Epub 2021 May 23.

Abstract

Congenital airway anomalies (CAA) include a variety of conditions that cause respiratory distress in neonates and infants. These malformations occur at various anatomic levels and manifest in a wide spectrum of airway symptoms, with presentation significantly influenced by the level at which obstruction occurs as well as by the severity of obstruction. The prevalence of congenital airway malformations has been estimated to range between 0.2 and 1 in 10,000 live births. The most frequent CAA are laryngomalacia, bilateral vocal cord paralysis, subglottic stenosis, laryngeal webs, subglottic hemangioma, tracheomalacia, congenital tracheal stenosis, laryngotracheal cleft, and tracheal agenesis.

摘要

先天性气道异常(CAA)包括多种导致新生儿和婴儿呼吸困难的病症。这些畸形发生在各种解剖学水平,并以广泛的气道症状表现出来,其表现明显受到梗阻部位以及梗阻严重程度的影响。先天性气道畸形的患病率估计在每 10000 例活产儿中有 0.2 至 1 例。最常见的 CAA 是喉软化、双侧声带麻痹、声门下狭窄、喉蹼、声门下血管瘤、气管软化、先天性气管狭窄、喉气管裂和气管发育不全。

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