Suppr超能文献

一名年轻西班牙裔男性大网膜来源的胃肠道外间质瘤

An Extragastrointestinal Stromal Tumor Arising From the Omentum in a Young Hispanic Male.

作者信息

DeRon Nathan, Khan Huda N

机构信息

Internal Medicine, Methodist Health System, Dallas, USA.

出版信息

Cureus. 2024 Apr 23;16(4):e58824. doi: 10.7759/cureus.58824. eCollection 2024 Apr.

Abstract

Gastrointestinal stromal tumors (GISTs) are neoplasms arising from the bowel wall, most often in the jejunoileum of the small intestine, but rarely from extragastrointestinal locations. GISTs most often occur in patients older than 40 years of age and can present with a multitude of gastrointestinal symptoms. We present a rare case of an extragastrointestinal stromal tumor (EGIST) causing abdominal pain and melena in a 34-year-old Hispanic male. The patient presented with diffuse abdominal pain, melena, and severe anemia. Computed tomography of the abdomen revealed a large mass abutting the small bowel. The patient was taken to surgery where the mass, which appeared to be deriving from the omentum and invading the adjacent small bowel, was completely excised and found to be a spindle cell GIST. Excision margins were determined to be negative, and the patient was started on a tyrosine kinase inhibitor for maintenance therapy. The patient continues to follow up on an outpatient basis for surveillance. This case represents the rare disease entity EGIST presenting outside the typical demographics of the disease in a young patient with no identified previous genetic syndromes. Gross examination of the mass in this case was also atypical given the appearance that the mass was rooted in the omentum and invading the small bowel which would suggest the primary tumor site was extragastrointestinal. This case demonstrates the need to build a differential diagnosis that includes GIST and the ability to successfully treat this disease if it is identified early in the clinical course.

摘要

胃肠道间质瘤(GISTs)是起源于肠壁的肿瘤,最常见于小肠空肠回肠段,但很少起源于胃肠道外部位。GISTs最常发生于40岁以上患者,可出现多种胃肠道症状。我们报告一例罕见的胃肠道外间质瘤(EGIST),导致一名34岁西班牙裔男性出现腹痛和黑便。该患者表现为弥漫性腹痛、黑便和严重贫血。腹部计算机断层扫描显示一个大肿块紧邻小肠。患者接受手术,肿块似乎起源于网膜并侵犯相邻小肠,被完整切除,病理结果为梭形细胞GIST。切除边缘确定为阴性,患者开始接受酪氨酸激酶抑制剂维持治疗。患者继续在门诊随访监测。该病例代表了罕见的疾病实体EGIST,在一名无既往明确遗传综合征的年轻患者中表现出与该疾病典型人口统计学特征不符的情况。鉴于肿块起源于网膜并侵犯小肠,提示原发肿瘤部位为胃肠道外,该病例肿块的大体检查也不典型。该病例表明,需要建立包括GIST在内的鉴别诊断,并且如果在临床病程早期确诊,有能力成功治疗该疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9293/11114087/16ec878b67cf/cureus-0016-00000058824-i01.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验