A rare case of duplication of the descending colon in a pregnant woman: case report and literature review

A rare case of duplication of the descending colon in a pregnant woman: case report and literature review

Authors

  • Vittorio Cherchi a:1:{s:5:"en_US";s:81:"University Hospital of Udine - General Surgery Clinic and Liver Transplant Center";}
  • Sergio Intini General Surgery Clinic and Liver Transplant Center, University Hospital of Udine, Udine, Italy
  • Jaqueline Velkoski General Surgery Clinic and Liver Transplant Center, University Hospital of Udine, Udine, Italy
  • Sergio Calandra General Surgery Clinic and Liver Transplant Center, University Hospital of Udine, Udine, Italy
  • Marco Ventin Department of Medical Area (DAME), University of Udine, Udine, Italy
  • Monica Della Martina Clinic of Obstetrics and Gynecology, University Hospital of Udine, Udine, Italy
  • Dario Lorenzin General Surgery Clinic and Liver Transplant Center, University Hospital of Udine, Udine, Italy
  • Lorenza Driul Clinic of Obstetrics and Gynecology, University Hospital of Udine, Udine, Italy
  • Giovanni Terrosu General Surgery Clinic and Liver Transplant Center, University Hospital of Udine, Udine, Italy

Keywords:

intestinal duplication; colonic duplication;, acute abdomen; pregnancy;, caesarean birth

Abstract

Introduction: Gastrointestinal duplications are uncommon congenital abnormalities that can occur anywhere throughout the intestinal tract. The small bowel is more interested than the large one. Duplications are schematically classified as spherical and tubular, respectively representing 80% and 20% of cases, with different relationships and communications with the native intestinal wall. Although typically diagnosed during infancy and early childhood, tubular colonic sub-type stays frequently hidden for several years until a complication occurs.

Case presentation: we report the case of a T-shaped tubular duplication in a 20-year-old woman at the 30th week of gestation, who underwent an urgent exploratory laparotomy for intestinal occlusion, treated with the resection of the aberrant large bowel. The patient was notable for a long history of constipation and chronic pain. Diagnostic possibilities were limited by the on-going pregnancy.

Conclusion: Intestinal duplications are uncommon malformations, and, of these, the T-shaped subtype of the colon is among the rarest ones. In the adulthood, diagnosis is usually established in the operating room during urgent or even emergency surgery performed for abdominal complications. A duplication of the descending colon is extremely rare, and this is, to our knowledge, the only article describing a case found in advanced state of pregnancy.

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Published

31-01-2023

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Section

Case Reports: General Surgery and Miscellanea

How to Cite

1.
Cherchi V, Intini S, Velkoski J, Calandra S, Ventin M, Della Martina M, et al. A rare case of duplication of the descending colon in a pregnant woman: case report and literature review. Acta Biomed [Internet]. 2023 Jan. 31 [cited 2024 Jul. 18];94(S1):e2023042. Available from: https://mattioli1885journals.com/index.php/actabiomedica/article/view/12169