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重新审视与加德纳综合征相关的多系统硬纤维瘤:一例临床病例

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

作者信息

Zhang Haijia, Wu Yongjie, Dong Xiushan, An Jie

机构信息

General Surgery Department, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, Taiyuan 030000, China.

出版信息

Case Rep Gastrointest Med. 2025 Feb 28;2025:6882566. doi: 10.1155/crgm/6882566. eCollection 2025.

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.

摘要

家族性腺瘤性息肉病(FAP)的一种变异型,即加德纳综合征(GS),可表现为肠外肿瘤,如硬纤维瘤(DTs)。临床医生在诊断过程中起着关键作用。由于DT常在肠道息肉形成之前出现,医生可通过寻找DT的特征性迹象早期识别潜在疾病。然而,在这种情况下,患者在腹壁肿瘤切除后未能及时认识到疾病,导致诊断延误并影响了疾病进程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9936/11991836/98696d4d8a38/CRIGM2025-6882566.001.jpg

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