Case Report: Caecal volvulus management from diagnosis to treatment in a young patient.


Journal

F1000Research
ISSN: 2046-1402
Titre abrégé: F1000Res
Pays: England
ID NLM: 101594320

Informations de publication

Date de publication:
2022
Historique:
accepted: 30 06 2022
entrez: 24 8 2022
pubmed: 25 8 2022
medline: 26 8 2022
Statut: epublish

Résumé

Caecal volvulus (CV) is a rare cause of intestinal obstruction, defined by an axial torsion of the caecum, ascending colon, and terminal ileum around the mesenteric vascular pedicles, leading to ischemia and bowel necrosis. A 20-year-old woman, with no significant medical history, was admitted for generalized abdominal pain evolving for three days, along with constipation and abdominal distension, but with no vomiting. Physical examination showed a generalized abdominal tenderness with no rigidity or rebound tenderness, associated with abdominal distension and tympanic upon percussion. Laboratory findings were within normal limits. An abdominal computed tomography scan revealed distension of a loop of the large bowel with its long axis extending from the right lower quadrant to the epigastrium or left upper quadrant. Colonic haustral pattern was absent. An abdominal computed tomography scan showed a rounded focal collection of air-distended bowel with haustral creases in the upper left quadrant. In addition, spiraled loops of the collapsed cecum (giving a whirl sign) were noted, along with low-attenuating fatty mesentery from the twisted bowel. The patient underwent an emergency laparotomy and caecectomy using GEA 80 charges. The patient had no complaints post-operation. CV is a rare cause of bowel obstruction, mainly caused by an exceedingly mobile caecum. Despite its rareness, CV represents the second most common cause of large bowel volvulus, behind sigmoid volvulus. For acute obstruction by CV, it is hard to differentiate it clinically from obstruction of the small bowel; therefore, radiological exams are needed. Surgery is the gold standard treatment for CV. We report a rare case of CV to highlight the rarity of this pathology, specify its diagnostic and therapeutic means, and its clinical and biological evolution.

Identifiants

pubmed: 35999844
doi: 10.12688/f1000research.121789.1
pmc: PMC9360906
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

781

Informations de copyright

Copyright: © 2022 Abbassi I et al.

Déclaration de conflit d'intérêts

No competing interests were disclosed.

Références

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Auteurs

Imed Abbassi (I)

General Surgery Department, Hôpital Universitaire Bougatfa of Bizerte, Bizerte, 7000, Tunisia.

Wissem Triki (W)

General Surgery Department, Hôpital Universitaire Bougatfa of Bizerte, Bizerte, 7000, Tunisia.

Racem Trigui (R)

General Surgery Department, Hôpital Universitaire Bougatfa of Bizerte, Bizerte, 7000, Tunisia.

Ahmed Itaimi (A)

General Surgery Department, Hôpital Universitaire Bougatfa of Bizerte, Bizerte, 7000, Tunisia.

Karim Ayed (K)

General Surgery Department, Hôpital Universitaire Bougatfa of Bizerte, Bizerte, 7000, Tunisia.

Hajer Sebri (H)

Gynecology and Obstetric Department, Hospital Mongi Slim of La Marsa, Tunis, 1000, Tunisia.

Oussema Baraket (O)

General Surgery Department, Hôpital Universitaire Bougatfa of Bizerte, Bizerte, 7000, Tunisia.

Sami Bouchoucha (S)

General Surgery Department, Hôpital Universitaire Bougatfa of Bizerte, Bizerte, 7000, Tunisia.

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