Midgut Volvulus as a Complication of Intestinal Malrotation in Pregnancy

A 38-year-old woman in the 27th week of gestation was admitted for sudden onset of epigastric pain, vomiting, and nausea, which worsened after food ingestion. The patient described 1 year of self-limited episodes of abdominal pain that improved with defecation and were associated with a change in frequency and consistency of stools that were interpreted as irritable bowel syndrome. On physical examination, she had stable vital signs, a distended abdomen, and tenderness in both upper quadrants. Blood tests showed leukocytosis 21.8 x 10/L and Creactive protein 10 mg/L. Abdominal x-ray was normal, and abdominal ultrasonography revealed a small amount of anechogenic fluid between intestinal loops and in the hepatorenal recess. Obstetric ultrasonography showed fetal well-being. Upper endoscopy was inconclusive because of abundant gastric residual fluid. Contrast-enhanced magnetic resonance imaging revealed features of malrotation (the large bowel was predominantly located on the left side and the small bowel predominantly on the right side) and a whirlpool image in the proximal small bowel (Figure 1). A diagnosis of a small bowel volvulus and midgut malrotation was made. Due to the risk of miscarriage, the patient refused surgery, and a conservative management with antibiotics, intravenous fluids, and parenteral nutrition was started. One week later, although the patient presented with normal vital signs, the abdominal pain and vomiting worsened and there was an increase in C-reactive protein to 102 mg/L. The patient accepted surgery, which confirmed the midgut malrotation associated with small bowel volvulus, and a Ladd’s procedure was done (Figure 2). Treitz ligament was absent. No complications were described postoperatively, and she gave birth to a healthy newborn with no apparent malformations at 38 weeks gestation.