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CASE REPORT
Year : 2019  |  Volume : 6  |  Issue : 4  |  Page : 262-264

Situs inversus totalis with symptomatic cholelithiasis: A diagnostic dilemma


1 Department of Gastroenterology, IGMC, Shimla, Himachal Pradesh, India
2 Department of Surgery, IGMC, Shimla, Himachal Pradesh, India
3 Department of Radiology, IGMC, Shimla, Himachal Pradesh, India

Correspondence Address:
Vishal Bodh
Department of Gastroenterology, IGMC, Shimla, Himachal Pradesh
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/cjhr.cjhr_96_18

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Situs inversus is a rare autosomal recessive condition, with incidence that varies from 1 in 5000 to 1 in 20,000 live births. Because of the atypical “mirror-image” anatomy associated with situs inversus, diagnosis of gallstone disease in these patients is difficult, especially in those with an unknown history of this condition. We report a case of a young female suspected to have situs inversus on esophagogastroduodenoscopy. Subsequently, she was confirmed to have situs inversus totalis with symptomatic cholelithiasis. She was managed successfully with single-incision laparoscopic cholecystectomy by a right-handed surgeon.


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