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Published on: May 19, 2022
Retrorectal tumor: a single-center 10-years' experience
Orçun Yalav1, Uğur Topal1, İsmail Cem Eray1
1Department of General Surgery, Çukurova University Faculty of Medicine, Adana, Turkey.
Retrorectal tumors (RTs) are rare, and this study evaluated surgical outcomes for 20 patients. Complete resection is crucial for long-term survival, with multidisciplinary management recommended for these complex tumors.
Area of Science:
- Surgical Oncology
- Gastroenterology
- Radiology
Background:
- Retrorectal tumors (RTs) are uncommon, with limited established guidelines for optimal surgical management.
- The complexity and heterogeneity of RTs necessitate careful evaluation and planning.
Purpose of the Study:
- To assess the surgical outcomes and long-term follow-up results for patients undergoing excision of retrorectal tumors (RTs).
- To contribute to the understanding of best practices for managing these rare neoplasms.
Main Methods:
- A retrospective review of 20 patients who underwent surgery for RTs between January 2009 and January 2019.
- Evaluation included demographic data, symptoms, diagnostic imaging (MRI, CT), surgical approaches, histopathology, complications, hospital stay, and mortality/readmission rates.
Main Results:
- The mean age of patients was 48.3 years; perineal pain was the most frequent symptom (35%).
- The posterior surgical approach was used for 14 patients with tumors below the third sacral vertebra.
- No postoperative mortality was observed; mean hospital stay was 8.6 days, with a 10% 90-day readmission rate. One recurrence (chordoma) was noted.
Conclusions:
- Management of retrorectal tumors (RTs) requires a multidisciplinary team approach due to tumor complexity.
- Detailed radiological imaging and a thorough understanding of pelvic anatomy are vital for surgical planning.
- Complete surgical resection is essential for achieving prolonged disease-free and overall survival in patients with RTs.
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