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

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...

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Main Authors: Haijia Zhang, Yongjie Wu, Xiushan Dong, Jie An
Format: Article
Language:English
Published: Wiley 2025-01-01
Series:Case Reports in Gastrointestinal Medicine
Online Access:http://dx.doi.org/10.1155/crgm/6882566
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author Haijia Zhang
Yongjie Wu
Xiushan Dong
Jie An
author_facet Haijia Zhang
Yongjie Wu
Xiushan Dong
Jie An
author_sort Haijia Zhang
collection DOAJ
description 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.
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series Case Reports in Gastrointestinal Medicine
spelling doaj-art-757d1d6790fa4eb7bbbf2628e5b5d5652025-08-20T03:06:30ZengWileyCase Reports in Gastrointestinal Medicine2090-65362025-01-01202510.1155/crgm/6882566Reexamining Multisystem Desmoid Tumors Linked to Gardner’s Syndrome: A Clinical CaseHaijia Zhang0Yongjie Wu1Xiushan Dong2Jie An3General Surgery DepartmentGeneral Surgery DepartmentGeneral Surgery DepartmentGeneral Surgery DepartmentA 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.http://dx.doi.org/10.1155/crgm/6882566
spellingShingle Haijia Zhang
Yongjie Wu
Xiushan Dong
Jie An
Reexamining Multisystem Desmoid Tumors Linked to Gardner’s Syndrome: A Clinical Case
Case Reports in Gastrointestinal Medicine
title Reexamining Multisystem Desmoid Tumors Linked to Gardner’s Syndrome: A Clinical Case
title_full Reexamining Multisystem Desmoid Tumors Linked to Gardner’s Syndrome: A Clinical Case
title_fullStr Reexamining Multisystem Desmoid Tumors Linked to Gardner’s Syndrome: A Clinical Case
title_full_unstemmed Reexamining Multisystem Desmoid Tumors Linked to Gardner’s Syndrome: A Clinical Case
title_short Reexamining Multisystem Desmoid Tumors Linked to Gardner’s Syndrome: A Clinical Case
title_sort reexamining multisystem desmoid tumors linked to gardner s syndrome a clinical case
url http://dx.doi.org/10.1155/crgm/6882566
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AT xiushandong reexaminingmultisystemdesmoidtumorslinkedtogardnerssyndromeaclinicalcase
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