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ASYMPTOMATIC SITUS AMBIGUOUS WITH LEFT- SIDED ISOMERISM & POLYSPLENIA : AN UNUSUAL INCIDENTAL PRESENTATION sejalgrover98@gmail.com

PE006
ASYMPTOMATIC SITUS AMBIGUOUS WITH LEFT- SIDED ISOMERISM & POLYSPLENIA : AN UNUSUAL INCIDENTAL PRESENTATION
Author Details
2
Including the presenting author
Sejal Grover sejalgrover98@gmail.com Lokmanya Tilak Municipal Medical College & General Hospital, Mumbai Department of General Surgery Mumbai India *
K. S. Sethna kssethna@yahoo.co.uk Lokmanya Tilak Municipal Medical College & General Hospital, Mumbai Department of General Surgery Mumbai India
 
 
 
 
 
 
 
 
 
 
Sejal Grover
sejalgrover98@gmail.com
India
Abstract
Oral or Poster
The first anatomical-clinical description of this type of pathology was made by Helwig EB in 1929 as a type of situs ambiguous characterized by left isomerism, associated with a group of visceral anomalies of unknown etiology, which includes the presence of splenic nodules outliers. The term left isomerism includes a group of morphological variations that cause part of the internal organs to be located to the right side of the midline with their tendency to adopt characteristics of those of the same name on the left side.
Incidental detection on radiographs during pre-operative evaluation
On the CT (computed tomograph) examination with contrast material, the following can be observed: Liver is predominately in the midline more on the left side. Stomach is distended and is on right side with gastro-duodenal junction seen in the midline. GB is in midline and fundus slightly towards left side. Multiple spleens (3) suggestive of polysplenia in the right hypochondrium with entire duodenum in the midline and towards left, anterior to head of pancreas. Part of body and tail of pancreas are not visualized suggestive of dorsal pancreatic agenesis. Head and uncinate process of pancreas seen towards the left of midline with body seen in the midline. Reversal of SMA-SMV relation with SMA noted right and posterior to the SMV.
This case contributes to the limited literature on this rare abnormality. The treatment and follow-up of patients with heterotaxy syndrome are not standardized and must be personalized according to each patient's unique symptoms and findigs.
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Category
1 General Topics organized by ISS/SIC
1.01 Basic Science
Submitted
249
Abstract Prizes
No
- Presenting author must register to the congress by 30 November 2025
- Author must submit a full-length manuscript conforming to the format of orignial articles in the World Journal of Surgery WJS by 30 November 2025
No
- Author must be age 40 or younger
- One of the authors must be a member of ISDS
- Presenting author must register to the congress by 30 November 2025
- Author must submit a full-length manuscript to the World Journal of Surgery WJS by 30 November 2025
No
- Author must be age 40 or younger
- One of the authors must be a member of ISDS
- Presenting author must register to the congress by 30 November 2025
- Author must submit a full-length manuscript to the World Journal of Surgery WJS by 30 November 2025