Aim: Retrorectal tumors are rare and heterogeneous. They are often asymptomatic or present with nonspecific symptoms, making management challenging. This study examines the diagnosis and treatment of retrorectal tumors.
Methods: Between 2002 and 2022, 21 patients with retrorectal tumors were treated in our department. We analyzed patient characteristics, diagnosis and treatment modalities retrospectively. Additionally, a literature review (2002-2023, "retrorectal tumors" and "presacral tumors", 20 or more cases included) was performed.
Results: Of the 21 patients (median age 54 years, 62% female), 17 patients (81%) suffered from benign lesions and 4 (19%) from malignant lesions. Symptoms were mostly nonspecific, with pain being the most common (11/21 (52%)). Diagnosis was incidental in eight cases. Magnetic resonance imaging was performed in 20 (95%) and biopsy was obtained in 10 (48%). Twenty patients underwent surgery, mostly via a posterior approach (14/20 (70%)). At a mean follow-up of 42 months (median 10 months, range 1-166 months), the local recurrence rate was 19%. There was no mortality. Our Pubmed search identified 39 publications.
Conclusion: Our data confirms the significant heterogeneity of retrorectal tumors, which poses a challenge to management, especially considering the often nonspecific symptoms. Regarding diagnosis and treatment, our data highlights the importance of MRI and surgical resection. In particular a malignancy rate of almost 20% warrants a surgical resection in case of the findings of a retrorectal tumour. A local recurrence rate of 19% supports the need for follow up.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11401784 | PMC |
http://dx.doi.org/10.1007/s00423-024-03471-0 | DOI Listing |
J Minim Invasive Surg
December 2024
Department of Surgery, Chonnam National University Hospital, Gwangju, Korea.
Retrorectal tumors, although rare, pose diagnostic and treatment challenges due to their nonspecific symptoms and complex anatomical location. This single-center case series reports short-term outcomes of laparoscopic transabdominal resection as a surgical approach for large retrorectal tumors. Between 2017 and 2020, five patients underwent this procedure.
View Article and Find Full Text PDFJ Surg Case Rep
November 2024
Surgery Department, Darwish Nazal Governmental Hospital, Ministry of Health, Darwish Nazal Hospital St., Qalqileyah 00970, Palestine.
Semin Oncol
December 2024
Department General and Digestive Surgery Coloproctology, Hospital Universitario de Burgos, Burgos, Spain.
Retrorectal cystic hamartoma (also known as tailgut cyst) is a congenital lesion that originates from debris from the embryonic caudal intestine. Incidentally diagnosed in more than half of cases, the treatment of choice is surgical resection. It is a very rare pathology whose oncological transformation constitutes a true pathological rarity.
View Article and Find Full Text PDFCureus
October 2024
General Surgery, Postgraduate Institute, Yashwantrao Chavan Memorial Hospital, Pimpri, Pune, IND.
Tailgut cysts are rare congenital cysts that develop from the embryological remnants of the gut. They are usually found in the retrorectal space. In most of the cases, they are asymptomatic.
View Article and Find Full Text PDFJ Visc Surg
October 2024
Digestive Surgery Department, Hôpital d'instruction des Armées Bégin, 69, avenue de Paris, 94160 Saint-Mandé, France; Inserm, University of Rennes, Oncogenesis, Stress, Signaling (OSS) Unit, UMR_S 1242, Rennes, France. Electronic address:
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!