Reexamining Multisystem Desmoid Tumors Linked to Gardner's Syndrome: A Clinical Case.

Haijia Zhang, Yongjie Wu, Xiushan Dong, Jie An

Abstract readCase Reports

In one paragraph

Article in Case reports in gastrointestinal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Haijia ZhangGeneral Surgery Department, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, Taiyuan 030000, China.ORCID https://orcid.org/0000-0001-9458-7970

Yongjie WuGeneral Surgery Department, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, Taiyuan 030000, China.ORCID https://orcid.org/0009-0009-2177-0083

Xiushan DongGeneral Surgery Department, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, Taiyuan 030000, China.ORCID https://orcid.org/0000-0001-7387-7303

Jie AnGeneral Surgery Department, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, Taiyuan 030000, China.ORCID https://orcid.org/0009-0003-2743-2209

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A variation of familial adenomatous polyposis (FAP), known as Gardner's syndrome (GS), can manifest as extraintestinal tumors, such as desmoid tumors (DTs). A key part in the diagnosing process is played by the clinician. Because DT frequently occurs before intestinal polyposis develops, doctors can identify the underlying illness early by looking for DT's telltale signs. Nevertheless, in this instance, the patient's failure to recognize the illness promptly following the excision of the tumor in the abdomen wall caused a delay in the diagnosis and impacted the disease's course.

Indexed as

desmoid tumor (DT)familial adenomatous polyposis (FAP)Gardner's syndrome (GS)

Identifiers

PMID40225021

DOI10.1155/crgm/6882566

PMCPMC11991836

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