A Case Report of Duodenal Diaphragm Misdiagnosed as a Bulimia.
- Author:
Yong Joo LEE
;
Eun Kyeong LEE
;
Kyeong Bin RHO
;
Yun Lyeon KIM
;
Suk Ja CHOI
;
Yong Joo KIM
- Publication Type:Case Report
- Keywords:
Duodenal diaphragm;
Duodenal obstruction
- MeSH:
Abdomen;
Abdominal Pain;
Bezoars;
Bulimia*;
Child, Preschool;
Diagnosis;
Diaphragm*;
Duodenal Obstruction;
Duodenum;
Failure to Thrive;
Female;
Humans;
Membranes;
Parturition;
Vomiting;
Weight Gain;
X-Ray Film
- From:Korean Journal of Gastrointestinal Endoscopy
1995;15(3):545-551
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Duodenal diaphragm is a rare congenital anomaly among the congenital duodenal obstructions. Its symptom and sign usually appear since birth if obstruction is complete. The clinical manifestations of incompletely obstructive duodenal diaphragm are intermittent vomiting, abdominal pain and poor weight gain. Diagnosis may be delayed in this case. Authors experienced a case of incomplete duodenal diaphragm with a central hole. A 29 months old girl presented failure to thrive, intermittent episodes of bloating, abdominal discomfort and occasional vomiting. The patient vomited every 10-14 days, then the abdominal pain and distention were relieved. She overate for about 10 days until the next projectile vomiting. The vomitus frequently contained food ingested several days previously. Plain x-ray films of abdomen showed marked gastric distention. Upper gastrointestinal series revealed marked distention of the duodenum with windsock configuration and radiolucent line at the third portion of the duodenum. On gastroscopic examination, gastric bezoar impacting the pyloric canal and antrum was noted. At operation, we found mucosal membrane in the third portion of the duodenum and bezoar(Chinese cabbage) above the membrane. Side-to-side duodeno-jejunostomy was performed and bezoar was removed. She was discharged on the 13th postoperative day without any complication.
