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Case Report
Copyright: ©Author(s) 2026.
World J Gastrointest Surg. Jun 27, 2026; 18(6): 119179
Published online Jun 27, 2026. doi: 10.4240/wjgs.119179
Table 1 Demographic characteristics and clinical presentation of reported situs inversus totalis patients undergoing laparoscopic cholecystectomy (n = 110), mean ± SD/n (%)
Variables
Value
Demographics
Age, years (n = 109)47.2 ± 12.8
Age, years (range)20-76
Sex
Male28 (25.5)
Female82 (74.5)
Preoperative diagnosis
Chronic cholecystitis38 (34.6)
Acute cholecystitis27 (24.4)
Cholelithiasis/symptomatic gallstone disease43 (39.1)
Other2 (1.8)
Primary pain location
Left upper quadrant/hypochondrium71 (65.1)
Epigastric28 (25.7)
Right upper quadrant3 (2.8)
Other/not specified7 (6.4)
Table 2 As-reported preoperative investigations in reported situs inversus totalis-laparoscopic cholecystectomy cases (n = 110), n (%)
Variables
Value
Ultrasonography98 (89.1)
Abdominal computed tomography43 (39.1)
Magnetic resonance imaging6 (5.5)
Magnetic resonance cholangiopancreatography14 (12.7)
Chest radiography76 (69.1)
Preoperative endoscopic retrograde cholangiopancreatography4 (3.6)
Table 3 Operative set-up and technical adaptations in reported situs inversus totalis-laparoscopic cholecystectomy cases (n = 110), n (%)
Variables
Value
Surgeon handedness
Right-handed79 (71.8)
Left-handed3 (2.7)
Ambidextrous/two-surgeon1 (0.9)
Other/not reported27 (24.5)
Primary surgeon position
Surgeon on patient’s right side86 (78.2)
Surgeon on patient’s left side5 (4.5)
Surgeon between the legs12 (10.9)
Other/not reported7 (6.4)
Port strategy
3-port12 (10.9)
4-port81 (73.6)
5-port5 (4.5)
Single-incision laparoscopic surgery12 (10.9)
Table 4 Perioperative outcomes in reported situs inversus totalis-laparoscopic cholecystectomy cases (n = 110), median (interquartile range)/n (%)
Variables
Value
Operative time, minutes (n = 66)65 (50-80)
Operative time, minutes (range)30-135
Postoperative stay, days (n = 99)2 (1-3)
Postoperative stay range, days1-8
Postoperative adverse events
Adverse event reported2 (1.8)
No adverse event reported99 (90.0)
Adverse event not reported9 (8.2)


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