Esophageal malformations

Steven W. Bruch; Arnold G. Coran; Shaun M. Kunisaki

doi:10.1007/978-88-470-5202-4_9

Esophageal malformations

Steven W. Bruch, Arnold G. Coran, Shaun M. Kunisaki

Research output: Chapter in Book/Report/Conference proceeding › Chapter

Abstract

LCs are rare congenital anomalies consisting of a midline defect along the posterior portion of the larynx and trachea as well as the anterior portion of the esophagus, leaving a communication between these structures of varying lengths. Pattersson carried out the first successful repair of a LC in 1955 [1]. Benjamin and Inglis classified LCs into four types. Type I is a supraglottic interarytenoid cleft. Type II extends into (but not through) the posterior cricoid lamina. Type III extends through the cricoid and can involve the cervical trachea. Type IV extends below the thoracic inlet [2].

Original language	English (US)
Title of host publication	Pediatric Thoracic Surgery
Publisher	Springer-Verlag Milan
Pages	111-119
Number of pages	9
ISBN (Electronic)	9788847052024
ISBN (Print)	9788847052017
DOIs	https://doi.org/10.1007/978-88-470-5202-4_9
State	Published - Jan 1 2013
Externally published	Yes

ASJC Scopus subject areas

Medicine(all)

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10.1007/978-88-470-5202-4_9

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AU - Coran, Arnold G.

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AB - LCs are rare congenital anomalies consisting of a midline defect along the posterior portion of the larynx and trachea as well as the anterior portion of the esophagus, leaving a communication between these structures of varying lengths. Pattersson carried out the first successful repair of a LC in 1955 [1]. Benjamin and Inglis classified LCs into four types. Type I is a supraglottic interarytenoid cleft. Type II extends into (but not through) the posterior cricoid lamina. Type III extends through the cricoid and can involve the cervical trachea. Type IV extends below the thoracic inlet [2].

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Esophageal malformations

Abstract

ASJC Scopus subject areas

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