TY - JOUR A1 - , T1 - A complete situs inversus viscerum with hepatic, intestinal and renalvascular anomalies: one case report and review of the literatur JO - Eur. J. Anat. SN - 1136-4890 Y1 - 2019 VL - 23 SP - 459 EP - 463 UR - http://www.eurjanat.com/web/paper.php?id=190379ob KW - Anatomy – Dissection – Situs inver-sus viscerum – Hepatic artery – Mesenteric arter-ies – Renal artery N2 - Situs inversus viscerum (SIV) is a rare congenital anomaly, which is still an intriguing phenomenon to anatomists and physicians alike. A complete SIV is characterized by a left-right transposition and mir-ror image of all thoraco-abdominal organs and their vasculature. The present report is based on one case with complete SIV, which was observed during the routine educational dissections of ca-davers in the authors’ Anatomy Department. A transposition of all truncal organs and their vascu-lature, and several variations of arteries and veins were present. The right branch of the proper he-patic artery was replaced by an artery that emanat-ed from the superior mesenteric artery. The latter also released the inferior mesenteric artery. Addi-tionally, a left accessory renal artery ran anterior to the inferior caval vein and posterior to the ureter to enter the hilum of the left kidney. There was also a variation in the anterior-posterior arrangement of the hilar structures of the left kidney. Additionally, a globally enlarged heart with coronary artery by-passes, a replaced aortic valve and an aortic arch aneurysm was observed. This case report is unique, as it presents a previously unreported co-incidence of SIV and hepatic, intestinal and renal vascular anomalies. It is important for the surgeon to be aware of such variations while planning an abdominal surgery in patients with SIV. ER -