Congenital Duodenal Web in a Young Adult
Journal of the Korean Surgical Society
;
: 343-347, 2003.
Article
in Korean
| WPRIM
| ID: wpr-36621
ABSTRACT
Congenital duodenal web in adult life is an extremely rare condition, which results from an incomplete recanalization of the duodenum during early embryologic development. We report a case of congenital duodenal web in a 23-year-old man who complained of postprandial epigastric pain and fullness, as well as nausea since childhood. The plain abdomen showed a double-bubble sign. The UGI study showed a marked dilatation of the proximal duodenum and a delayed passage of barium into the third portion of the duodenum. Abdominal ultrasonography and CT revealed a marked dilatation of the proximal duodenum and a duodenal web with windsock deformity, which originated from the ampulla of Vater and extended to the third portion of the duodenum. A winsock web with a 0.9 cm eccentric aperture and a healed ulcer proximal to the ampulla of Vater were observed during a longitudinal duodenotomy. The web was excised circumferentially and the duodenum was closed transversely in a Heineke-Mikulicz fashion.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Congenital Abnormalities
/
Ulcer
/
Barium
/
Ampulla of Vater
/
Ultrasonography
/
Dilatation
/
Duodenum
/
Abdomen
/
Nausea
Type of study:
Diagnostic study
Limits:
Adult
/
Humans
Language:
Korean
Journal:
Journal of the Korean Surgical Society
Year:
2003
Type:
Article
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