Document Detail


Congenital esophageal obstruction by intraluminal mucosal diaphragm.
MedLine Citation:
PMID:  2023088     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Congenital intraluminal esophageal diaphragm causing complete obstruction is a rare anomaly. By esophagoscopy, a complete membranous diaphragm was demonstrated, perforated, and excised. In the English language literature, this case represents the first report of an isolated membranous atresia at the lower end of the esophagus. A brief review of the world literature and the classification of membranous atresia of the esophagus is discussed.
Authors:
A K Sharma; K K Sharma; C S Sharma; S Chandra; M Udawat
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Publication Detail:
Type:  Case Reports; Journal Article; Review    
Journal Detail:
Title:  Journal of pediatric surgery     Volume:  26     ISSN:  0022-3468     ISO Abbreviation:  J. Pediatr. Surg.     Publication Date:  1991 Feb 
Date Detail:
Created Date:  1991-06-04     Completed Date:  1991-06-04     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0052631     Medline TA:  J Pediatr Surg     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  213-5     Citation Subset:  IM    
Affiliation:
Department of Surgery, S.M.S. Medical College, Jaipur, India.
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MeSH Terms
Descriptor/Qualifier:
Bronchopneumonia / etiology
Diaphragm / pathology
Esophageal Atresia / complications,  pathology*,  surgery
Humans
Infant, Newborn
Infant, Premature
Sepsis / etiology

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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