Abstract
A very rare case of multi-organ volvulus, serially involving the spleen, colon and stomach, is presented in a 24-year-old female patient with Down syndrome. This case is of interest because of the three different types of volvulus or torsion that occurred serially over thirteen years in the same patient. We report the imaging findings and suggest possible pathogenesis by a review of the operation record and literature.
References
1. Lehance CW, Gold DM. Colonic volvulus - an old problem with a new twist. Colorectal Dis. 2009; 11:882–883.
2. Learmonth JR. Elongation and dilatation of the colon. Br Med J. 1937; 2:154–156.
3. Bakir B, Poyanli A, Yekeler E, Acunas G. Acute torsion of a wandering spleen: imaging findings. Abdom Imaging. 2004; 29:707–709.
4. Herman TE, Siegel MJ. CT of acute splenic torsion in children with wandering spleen. AJR Am J Roentgenol. 1991; 156:151–153.
5. Berrocal T, Lamas M, Gutieerrez J, Torres I, Prieto C, del Hoyo ML. Congenital anomalies of the small intestine, colon, and rectum. Radiographics. 1999; 19:1219–1236.
6. Cherukupalli C, Khaneja S, Bankulla P, Schein M. CT diagnosis of acute gastric vovulus. Dig Surg. 2003; 20:497–499.
7. Kotobi H, Auber F, Otta E, Meyer N, Audry G, Helardot PG. Acute mesenteroaxial gastric volvulus and congenital diaphragmatic hernia. Pediatr Surg Int. 2005; 21:674–676.