Document Detail


Congenital duodenal membrane: a ten-year review.
MedLine Citation:
PMID:  10910590     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Traditionally, congenital duodenal membrane (CDM) has been classified as a type of duodenal atresia. To provide a better understanding of this disease entity, the experience of our 13 patients with congenital duodenal membrane treated from April 1988 to November 1998 is reported. Nine were boys and four were girls, including four prematures (31%). Late diagnosis was made in eight babies and led to prolonged hospitalization (mean 20 days), although duodenal obstruction was demonstrated by barium study in all 13 patients. The low frequency of bilious vomiting (46%) and abdominal distention (39%), and lack of definite findings on plain abdominal X-ray and abdominal ultrasonography, have contributed to the delayed diagnosis in our patients. Nevertheless, no major complications developed after web excision with duodenoplasty, and satisfactory weight gain was noted in all patients except the two with Down syndrome. Since CDM is often overlooked, a better understanding of this disease entity can prevent delayed diagnosis, growth retardation and prolonged hospitalization.
Authors:
F C Huang; J H Chuang; C S Shieh
Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi     Volume:  40     ISSN:  1608-8115     ISO Abbreviation:  Acta Paediatr Taiwan     Publication Date:    1999 Mar-Apr
Date Detail:
Created Date:  1999-06-15     Completed Date:  1999-06-15     Revised Date:  2005-11-16    
Medline Journal Info:
Nlm Unique ID:  100958202     Medline TA:  Acta Paediatr Taiwan     Country:  CHINA (REPUBLIC : 1949-)    
Other Details:
Languages:  eng     Pagination:  70-4     Citation Subset:  IM    
Affiliation:
Department of Pediatrics, Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
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MeSH Terms
Descriptor/Qualifier:
Child
Child, Preschool
Duodenal Obstruction / congenital*,  diagnosis,  surgery
Female
Humans
Infant
Infant, Newborn
Infant, Premature
Intestinal Atresia* / diagnosis,  surgery
Male
Treatment Outcome

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


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