Evidence map›Paper›PMID 42131449›Full record

ArticleSAGE open medical case reports2026

Desmoid tumor mimicking cancer recurrence in a patient with colon cancer and Gardner syndrome: A case report.

Jing Zhang, Yan Fu, Peng Zeng

Abstract readCase Reports
In one paragraph

Article in SAGE open medical 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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Jing ZhangMedical School, Southeast University, Nanjing, Jiangsu, China.
Yan FuDepartment of Interventional Therapy, National Cancer Center, National Clinical Research Center for Cancer, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Peng ZengDepartment of Oncology, Zhongda Hospital, Medical School, Southeast University, Nanjing, Jiangsu, China.ORCID https://orcid.org/0000-0003-1606-7528

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gardner syndrome, a subtype of familial adenomatous polyposis, features colorectal polyposis, osteomas and soft-tissue tumors with elevated colorectal carcinoma risk, and abdominal masses in these patients are easily misdiagnosed as malignant recurrence, especially with concomitant bone lesions. We report a 33-year-old female familial adenomatous polyposis patient with a history of surgically treated stage IIIA colorectal adenocarcinoma, who presented with a 3-month abdominal mass. Contrast-enhanced computed tomography indicated a large cystic-solid mass with lymphadenopathy and peritoneal thickening, suggesting recurrence, while magnetic resonance imaging suggested a desmoid tumor and identified bilateral femoral head avascular necrosis. Surgical resection and pathogenic adenomatous polyposis coli gene mutation detection confirmed an abdominal desmoid tumor. This case highlights that Gardner syndrome can induce benign space-occupying desmoid tumors, and for familial adenomatous polyposis patients with bone lesions, combining advanced imaging, histopathology and genetic testing is critical to avoid misdiagnosis and unnecessary interventions for suspected cancer recurrence.

Indexed as

case reportcolon cancerdesmoid fibromafamilial adenomatous polyposisGardner syndrome

Identifiers

PMID42131449
PMCPMC13161622

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Registered trials

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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.