Congenital esophageal stenosis
Identifieur interne : 00B988 ( Main/Exploration ); précédent : 00B987; suivant : 00B989Congenital 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 :
- Digestive Diseases and Sciences [ 0163-2116 ] ; 1990-02-01.
English descriptors
- KwdEn :
- Case report, Caustic, Caustic stricture, Congenital, Congenital esophageal stenosis, Diaphragmatic hiatus, Digestive diseases, Dilator, Eisenhower army, Endoscopic, Esophageal, Esophageal manometry, Esophageal peristalsis, Esophageal stenosis, Esophagus, February, Food impaction, Gastroenterology service, Impaction, Lower esophageal sphincter, Peristalsis, Poor dentition, Stenosis, Stenotic, Stricture, Walter reed army.
- Teeft :
- Case report, Caustic, Caustic stricture, Congenital, Congenital esophageal stenosis, Diaphragmatic hiatus, Digestive diseases, Dilator, Eisenhower army, Endoscopic, Esophageal, Esophageal manometry, Esophageal peristalsis, Esophageal stenosis, Esophagus, February, Food impaction, Gastroenterology service, Impaction, Lower esophageal sphincter, Peristalsis, Poor dentition, Stenosis, Stenotic, Stricture, Walter reed army.
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:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 003097
- to stream Istex, to step Curation: 003097
- to stream Istex, to step Checkpoint: 005771
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- to stream Main, to step Curation: 00B988
Le document en format XML
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<term>Digestive diseases</term>
<term>Dilator</term>
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<front><div type="abstract" xml:lang="en">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.</div>
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