Abstract
Intestinal malrotation is an uncommon cause of abdominal pain and normally presents during infancy. Familial cases of malrotation are extremely rare in the absence of other congenital malformations. We present the case of a 22-year-old woman with undiagnosed chronic abdominal pain and her previously well 16-year-old brother who presented within 18 months of each other with acute midgut volvulus secondary to intestinal malrotation. Clinicians should be aware of this rare but serious cause of abdominal pain.
Original language | English |
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Pages (from-to) | e191-2 |
Journal | Annals of the Royal College of Surgeons of England |
Volume | 94 |
Issue number | 6 |
DOIs | |
Publication status | Published - Sept 2012 |
Keywords
- Abdominal Pain
- Adolescent
- Cecal Diseases
- Delayed Diagnosis
- Duodenal Diseases
- Female
- Humans
- Intestinal Volvulus
- Male
- Siblings
- Tomography, X-Ray Computed
- Young Adult