Choledochal cyst in situs inversus totalis: Hitherto unreported association

Syed Aslam Shah, Qurrat Al Ain Atif, Iftikhar Ahmed Soomro, Muhammad Saaiq

Abstract


Situs inversus totalis is a rare autosomal recessive disorder characterized by transposition of the intra-abdominal as well as the intrathoracic viscera. We present the case of a 45-year-old Pakistani lady who had choledochal cyst with cholelithiasis in tandem with situs inversus totalis. We were faced with dilemmas both diagnostic and management during the course of her care. We share our experience with emphasis on both ultrasonologist as well as surgical team members to be mindful of the possibility of an underlying choledochal cyst when they are dealing with symptomatic gall stone disease in such patients. This will ensure appropriate surgical planning and avert the avoidable dilemmas intra-operatively.


Full Text: PDF DOI: 10.5430/crcp.v1n1p27

Refbacks

  • There are currently no refbacks.


Case Reports in Clinical Pathology

ISSN 2331-2726 (Print)  ISSN 2331-2734(Online)

Copyright © Sciedu Press

To make sure that you can receive messages from us, please add the 'sciedu.ca' and ‘sciedupress.com’ domains to your e-mail 'safe list'. If you do not receive e-mail in your 'inbox', please check your 'spam' or 'junk' folder.