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Congenital esophageal stenosis

Identifieur interne : 00B988 ( Main/Exploration ); précédent : 00B987; suivant : 00B989

Congenital esophageal stenosis

Auteurs : Peter R. Mcnally [Géorgie (pays), États-Unis] ; Captain Edward H. Collier Iii [Géorgie (pays), États-Unis] ; Captain Mark C. Lopiano [Géorgie (pays), États-Unis] ; Lieutenant Colonel Thomas G. Brewer [Géorgie (pays), États-Unis] ; Colonel Roy K. H. Wong [Géorgie (pays), États-Unis]

Source :

RBID : ISTEX:6359391339F93077C0CE9272DA15E525ABBA3760

English descriptors

Abstract

Abstract: Esophageal stenosis is a rare congenital anomaly (1 per 25,000 live births), which usually presents during infancy (1). The stenosis is typically aperistaltic, and the onset of symptoms depends upon the degree of deformity. In severe stenosis, symptoms of vomiting or r'egurgitation occur at birth or with the introduction of solids (2, 3). In mild cases, patient adaptation may delay the diagnosis (1,4). We report an unusual case of congenital esophageal stenosis, where abnormal peristalsis was preserved within the stenotic segment and presentation as acute food impaction was delayed until adulthood. Endoscopic, radiographic, and esophageal manometric findings of congenital esophageal stenosis are described, and the therapeutic alternatives discussed.

Url:
DOI: 10.1007/BF01536774


Affiliations:


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Le document en format XML

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