Suppr超能文献

以勒-特雷拉征为非典型炎症过程后遗症的病例报告。

Case report of Leser-Trelat sign as sequela of an atypical inflammatory process.

作者信息

Mulero-Soto P, Sanchez-Vivaldi J, Rovira O, Arocho J, Pereira-Torrellas G, Martinez-Trabal J, Bolaños-Avila G

机构信息

Department of General Surgery at St. Luke's Medical Center, Ponce Health Sciences University, Ponce, Puerto Rico.

出版信息

Int J Surg Case Rep. 2022 Mar;92:106833. doi: 10.1016/j.ijscr.2022.106833. Epub 2022 Feb 12.

Abstract

BACKGROUND

Leser-Trelat sign is a rare paraneoplastic syndrome in which one main characteristic presented is an eruption of multiple seborrheic keratoses around different areas of the body. This syndrome has been associated with multiple gastrointestinal malignancies, especially adenocarcinoma of stomach and colon.

CASE REPORT

We report a 70-year-old male who presented to the surgery clinic complaining of a persistent lower abdominal pain for the past 2 months. The pain was associated with weight loss and the gradual appearance of multiple seborrheic keratoses in his body. The patient was admitted to the hospital for further evaluation, a CT scan shows an 8.1 × 5.2 cm mass in the mid mesentery and laboratories shows anemia and positive fecal occult blood. The patient was scheduled for an exploratory laparotomy. During the surgery, a large mass was found arising from the ascending colon with invasion into the adjacent sigmoid colon. The mass was sent to pathology and shows a foreign body granuloma. In addition to the surgery, the patient undergoes an endoscopic evaluation to rule out a malignancy from the upper gastrointestinal system, no masses or lesions were found.

CONCLUSION

This is the first case reported, as far as our knowledge, of a foreign body granuloma in the association of Leser-Trelat sign. Foreign body granulomas are associated with multiple cellular signaling and this could be the source of the association of the Leser-Trelat sign. Further evaluation is needed to have a better understanding of the association between the Leser-Trelat sign and the formation of a foreign body granuloma.

摘要

背景

Leser-Trelat征是一种罕见的副肿瘤综合征,其主要特征之一是身体不同部位出现多发性脂溢性角化病。该综合征与多种胃肠道恶性肿瘤有关,尤其是胃和结肠腺癌。

病例报告

我们报告一名70岁男性,他到外科诊所就诊,主诉过去2个月持续下腹痛。疼痛伴有体重减轻,且身体逐渐出现多发性脂溢性角化病。患者入院进一步评估,CT扫描显示肠系膜中部有一个8.1×5.2厘米的肿块,实验室检查显示贫血和粪便潜血阳性。患者计划进行剖腹探查术。手术中,发现一个大肿块起源于升结肠并侵犯相邻的乙状结肠。肿块送去做病理检查,显示为异物肉芽肿。除手术外,患者还接受了内镜评估以排除上消化道系统的恶性肿瘤,未发现肿块或病变。

结论

据我们所知,这是首例报道的与Leser-Trelat征相关的异物肉芽肿病例。异物肉芽肿与多种细胞信号传导有关,这可能是Leser-Trelat征相关的原因。需要进一步评估以更好地了解Leser-Trelat征与异物肉芽肿形成之间的关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f10/8857496/89dd2cff8c57/gr1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验