Hemorragia de tubo digestivo secundaria a tumor del estroma gastrointestinal localizado en yeyuno. Reporte de un caso

IF 0.1 Q4 ONCOLOGY Gaceta Mexicana de Oncologia Pub Date : 2016-11-01 DOI:10.1016/j.gamo.2016.09.012
Fernando Navarro-Tovar , Edgar Hernández-Pérez , Héctor Alejandro Carzolio-Trujillo , José Manuel Aguilar-Priego , Iván Arturo Hernández-Martínez , Jorge Miguel García-Salazar
{"title":"Hemorragia de tubo digestivo secundaria a tumor del estroma gastrointestinal localizado en yeyuno. Reporte de un caso","authors":"Fernando Navarro-Tovar ,&nbsp;Edgar Hernández-Pérez ,&nbsp;Héctor Alejandro Carzolio-Trujillo ,&nbsp;José Manuel Aguilar-Priego ,&nbsp;Iván Arturo Hernández-Martínez ,&nbsp;Jorge Miguel García-Salazar","doi":"10.1016/j.gamo.2016.09.012","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Gastrointestinal stromal tumours (GIST) are rare, with around 20% being located in the small intestine. The most common clinical presentation is gastrointestinal bleeding, resulting from pressure necrosis and ulceration of the gastrointestinal mucosa, with laceration of the underlying vessels.</p></div><div><h3>Clinical case</h3><p>A 37-year old male, with clinical symptoms of obscure gastrointestinal bleeding. The endoscopy and colonoscopy showed no abnormalities, and an abdominal-pelvic tomography demonstrated a small bowel loop with a possible GIST being likely, due to the persistent gastrointestinal bleeding. An exploratory laparotomy it is performed, finding a tumour in the jejunum. An intestinal resection and end-to-end intestinal anastomosis was performed. With normal post-operative course, the patient was discharged on the fifth day, with histopathology reporting fusiform tumour cells and positive CD117, compatible with a stromal tumour.</p></div><div><h3>Discussion</h3><p>GISTs are derived from Cajal cells, and are characterised by mutations of c-KIT gene. They represent less than 1% of all digestive tract tumours, and occur most often in the stomach, followed by the small intestine. Its most common clinical presentation is gastrointestinal bleeding, representing 5-10% of cases when the origin is obscure. Part of surgical recommendations in the curative treatment of GIST are complete resection with negative surgical margins and pseudo-capsule (R0).</p></div><div><h3>Conclusions</h3><p>GISTs are a cause of gastrointestinal bleeding of obscure origin, with complete surgical resection being the only curative option.</p></div>","PeriodicalId":41581,"journal":{"name":"Gaceta Mexicana de Oncologia","volume":"15 6","pages":"Pages 375-380"},"PeriodicalIF":0.1000,"publicationDate":"2016-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.gamo.2016.09.012","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gaceta Mexicana de Oncologia","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1665920116300918","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Gastrointestinal stromal tumours (GIST) are rare, with around 20% being located in the small intestine. The most common clinical presentation is gastrointestinal bleeding, resulting from pressure necrosis and ulceration of the gastrointestinal mucosa, with laceration of the underlying vessels.

Clinical case

A 37-year old male, with clinical symptoms of obscure gastrointestinal bleeding. The endoscopy and colonoscopy showed no abnormalities, and an abdominal-pelvic tomography demonstrated a small bowel loop with a possible GIST being likely, due to the persistent gastrointestinal bleeding. An exploratory laparotomy it is performed, finding a tumour in the jejunum. An intestinal resection and end-to-end intestinal anastomosis was performed. With normal post-operative course, the patient was discharged on the fifth day, with histopathology reporting fusiform tumour cells and positive CD117, compatible with a stromal tumour.

Discussion

GISTs are derived from Cajal cells, and are characterised by mutations of c-KIT gene. They represent less than 1% of all digestive tract tumours, and occur most often in the stomach, followed by the small intestine. Its most common clinical presentation is gastrointestinal bleeding, representing 5-10% of cases when the origin is obscure. Part of surgical recommendations in the curative treatment of GIST are complete resection with negative surgical margins and pseudo-capsule (R0).

Conclusions

GISTs are a cause of gastrointestinal bleeding of obscure origin, with complete surgical resection being the only curative option.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
消化道出血继发于叶野胃肠道间质瘤。报告个案
胃肠道间质瘤(GIST)是罕见的,约20%位于小肠。最常见的临床表现是胃肠道出血,由胃肠粘膜压迫性坏死和溃疡引起,并伴有下层血管撕裂。临床病例男,37岁,临床表现为消化道出血。内窥镜和结肠镜检查未见异常,腹部-骨盆断层扫描显示小肠袢,由于持续的胃肠道出血,可能有胃肠道间质瘤。进行剖腹探查,在空肠发现肿瘤。行肠切除术和端对端肠吻合。术后过程正常,患者于第5天出院,组织病理学报告梭状肿瘤细胞和CD117阳性,与间质肿瘤相容。gist来源于Cajal细胞,以c-KIT基因突变为特征。它们在所有消化道肿瘤中所占比例不到1%,最常发生在胃,其次是小肠。其最常见的临床表现是消化道出血,在病因不明的病例中占5-10%。根治性GIST的部分手术建议是完全切除阴性切缘和假包膜(R0)。结论胃肠道间质瘤是一种原因不明的消化道出血,完全手术切除是唯一的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
0.10
自引率
0.00%
发文量
255
期刊最新文献
Breast cancer survival in Guerrero: oncologic care and geographic disparities in Mexico Comparative evaluation of three palliative external beam radiotherapy schedules in painful bone metastases Breast cancer methodology for maximization of resources currently used in Mexican centers Activación conductual y <i>mindfulness</i> en la experiencia del dolor de mujeres con cáncer de mama Response to conformal radiotherapy in head and neck paragangliomas
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1