侵袭性十二指肠炎性纤维化息肉1例。

IF 1.7 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Fen-Ming Zhang, Long-Gui Ning, Jing-Jie Wang, Hua-Tuo Zhu, Mei-Bao Feng, Hong-Tan Chen
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引用次数: 0

摘要

背景:胃肠道炎症性纤维化息肉(IFP)通常被认为是良性的、无创的。十二指肠的IFP是非常罕见的。我们在此报告一例类似恶性肿瘤的侵袭性和浸润性十二指肠IFP,患者随后接受手术治疗。据我们所知,这是第一例十二指肠IFP侵入浆膜下。病例总结:一名50岁女性患者,腹痛复发1个多月。胃镜检查显示十二指肠球部有肿块,累及幽门。内镜超声提示病变为低回声肿块,累及固有肌层,根据腹部计算机断层扫描和胃磁共振成像结果考虑十二指肠球间质瘤。随后行远端胃切除术。根据组织病理学和免疫组化结果,最终诊断为十二指肠IFP。患者术后恢复良好,随访27个月无复发。结论:十二指肠IFP侵袭浆膜下提示IFP具有特定的侵袭特征,准确诊断是避免治疗不当的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Invasive inflammatory fibrotic polyp of the duodenum: A case report.

Background: An inflammatory fibrotic polyp (IFP) of the gastrointestinal tract is generally considered benign and noninvasive. An IFP in the duodenum is very rare. Here we report the case of an aggressive and infiltrative duodenal IFP resembling a malignancy and the patient subsequently underwent surgery. To the best of our knowledge, this is the first case of duodenal IFP invading the subserosa.

Case summary: A 50-year-old female patient presented with recurrent epigastric pain for more than 1 month. Gastroscopy revealed a mass in the duodenal bulb involving the pylorus. Endoscopic ultrasound suggested that the lesion was a hypoechoic mass involving the muscularis propria, and duodenal bulb stromal tumor was considered based on abdominal computed tomography and gastric magnetic resonance imaging findings. A distal gastrectomy was subsequently performed. Based on the histopathology and immunohistochemical results, the lesion was finally diagnosed as duodenal IFP. The patient recovered well after surgery and had no recurrence at the 27-month follow-up.

Conclusion: This duodenal IFP invading subserosa indicates that IFP has specific invasion characteristics, and accurate diagnosis is critical to avoid inadequate treatment.

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