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: | , , , |
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| Format: | Article |
| Language: | English |
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Wiley
2025-01-01
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| 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. |
| format | Article |
| id | doaj-art-757d1d6790fa4eb7bbbf2628e5b5d565 |
| institution | DOAJ |
| issn | 2090-6536 |
| language | English |
| publishDate | 2025-01-01 |
| publisher | Wiley |
| record_format | Article |
| 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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