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Congenital intestinal duplication in an adult
Meha Goyal1, Hector Ivan Saucedo-Crespo, Francis Joseph Welsh
1Baylor College of Medicine, 1504 Taub Loop, Houston, TX, 77030, USA, mgoyal@bcm.edu.
Insights
Congenital intestinal duplication, a rare condition usually seen in children, can present in adults with vague abdominal symptoms. This case highlights the intraoperative diagnosis of this anomaly in a 33-year-old female.
Area of Science:
- Gastroenterology
- Pediatric Surgery
- Surgical Pathology
Background:
- Congenital intestinal duplication is a rare congenital anomaly.
- It is typically diagnosed in children under two years old.
- Adult presentation is uncommon, often with vague symptoms.
Abstract:
Congenital intestinal duplication is an anomaly most commonly diagnosed in children under the age of 2. Rarely, it is seen in adults who remain asymptomatic or present with vague abdominal symptoms. Here, we describe the case of a 33-year-old female who was diagnosed intraoperatively with congenital intestinal duplication after suffering from a year of vague abdominal complaints.
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