ArticleInternational journal of surgery case reports2026
Primary retroperitoneal pseudomyxoma masquerading as a benign retroperitoneal abscess from an ascending colon subacute perforation: a case report.
Article in International journal of surgery case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction and importance: Pseudomyxoma peritonei is a neoplastic process characterized by diffuse mucinous implants on peritoneal surfaces arising from mucin-producing tumors. Rarely, pseudomyxoma from a ruptured mucin-producing tumor can be confined to the retroperitoneum, termed "retroperitoneal pseudomyxoma" or "extraperitoneal pseudomyxoma." This entity often masquerades as a retroperitoneal abscess of benign etiology. Case presentation: A 58-year-old man presented with a symptomatic retroperitoneal cystic mass with a fistulous communication to the ascending colon seen at colonoscopy, without evidence of mucosal neoplasm. Operative exploration revealed a fixed mass in the retroperitoneum, resection was aborted, and diverting loop ileostomy and operative biopsy of the mass performed. Biopsy histology revealed "pseudomyxoma peritonei." Of note, the patient had undergone appendectomy 20 years previously. Three months after fecal diversion, the patient underwent further staging which revealed the tumor was abutting the right femoral nerve. En-Bloc resection of the mass was performed and the femoral nerve was spared. Histologic evaluation revealed a mucinous neoplasm of the appendix, with negative margins of resection. Clinical discussion: Primary retroperitoneal pseudomyxoma is a rare entity. The tumors often arise from a retroperitoneal appendix, although our patient had a prior appendectomy, increasing the diagnostic confusion. Histology confirmed that the tumor arose from the remnant appendiceal stump, and the fistula was malignant erosion into the colon. In this case, with no detectable peritoneal disease, primary treatment was radical resection with the goal of achieving negative margins. Conclusion: Primary retroperitoneal pseudomyxoma is rare, often arising from a retroperitoneal appendix. In the absence of peritoneal disease, radical resection may be considered definitive therapy.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.