Primary colonic liposarcoma presenting as intussusception: A case report from the Kashmir valley

Yaqoob Hassan, A. Rather, Z. Akhtar
{"title":"Primary colonic liposarcoma presenting as intussusception: A case report from the Kashmir valley","authors":"Yaqoob Hassan, A. Rather, Z. Akhtar","doi":"10.4103/hmj.hmj_76_21","DOIUrl":null,"url":null,"abstract":"Rationale: Soft tissue sarcoma (STS) arises from mesenchymal tissue and can occur at any anatomic site and age. These tumors can originate from skeletal muscle, adipose tissue, vascular tissues, or connective tissues. Liposarcoma (LPS) is the most frequent type of sarcoma and is commonly found in the retroperitoneal region. Patient Concerns: A case of colonic liposarcoma in a young female patient presented with sub-acute intestinal obstruction due to intussusception. The patient was only 17-years-old, much younger than the average age of occurrence, and thus represents the first case report of primary colonic liposarcoma in this age group. Diagnosis: The patient was resuscitated and subjected to standard investigations. An ultrasonography abdomen/ pelvis revealed colo-colic intussusception and CECT abdomen showed evidence of an enhancing mass within the lumen of the transverse colon. Interventions: The patient was subjected to exploratory laparotomy with segmental colonic resection and primary colo-colic anastomosis. Outcomes: The histopathology and immunohistochemistry revealed the morphology of high grade colonic liposarcoma. The patient is doing well eight months after surgery and is being monitored on a regular basis. Lessons: The primary gastrointestinal liposarcoma tumors are uncommon and colonic variants are extremely rare, especially in the second decade of life, and limited to case reports which can be counted on fingertips. Surgical resection with negative margins is the only curative treatment.","PeriodicalId":34280,"journal":{"name":"Hamdan Medical Journal","volume":"15 1","pages":"104 - 107"},"PeriodicalIF":0.0000,"publicationDate":"2022-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hamdan Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/hmj.hmj_76_21","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Rationale: Soft tissue sarcoma (STS) arises from mesenchymal tissue and can occur at any anatomic site and age. These tumors can originate from skeletal muscle, adipose tissue, vascular tissues, or connective tissues. Liposarcoma (LPS) is the most frequent type of sarcoma and is commonly found in the retroperitoneal region. Patient Concerns: A case of colonic liposarcoma in a young female patient presented with sub-acute intestinal obstruction due to intussusception. The patient was only 17-years-old, much younger than the average age of occurrence, and thus represents the first case report of primary colonic liposarcoma in this age group. Diagnosis: The patient was resuscitated and subjected to standard investigations. An ultrasonography abdomen/ pelvis revealed colo-colic intussusception and CECT abdomen showed evidence of an enhancing mass within the lumen of the transverse colon. Interventions: The patient was subjected to exploratory laparotomy with segmental colonic resection and primary colo-colic anastomosis. Outcomes: The histopathology and immunohistochemistry revealed the morphology of high grade colonic liposarcoma. The patient is doing well eight months after surgery and is being monitored on a regular basis. Lessons: The primary gastrointestinal liposarcoma tumors are uncommon and colonic variants are extremely rare, especially in the second decade of life, and limited to case reports which can be counted on fingertips. Surgical resection with negative margins is the only curative treatment.
以肠套叠为表现的原发性结肠脂肪肉瘤:一例来自克什米尔山谷的病例报告
理由:软组织肉瘤起源于间充质组织,可发生在任何解剖部位和年龄。这些肿瘤可以起源于骨骼肌、脂肪组织、血管组织或结缔组织。脂瘤(LPS)是最常见的肉瘤类型,常见于腹膜后区域。患者关注:一例年轻女性结肠脂肪肉瘤,因肠套叠引起亚急性肠梗阻。该患者只有17岁,比平均发病年龄年轻得多,因此是该年龄组第一例原发性结肠脂肪肉瘤病例报告。诊断:患者被复苏并接受标准检查。腹部/骨盆超声检查显示结肠肠套叠,CECT腹部显示横结肠腔内肿块增强。干预措施:患者接受了剖腹探查术,包括结肠节段切除和结肠-结肠吻合。结果:组织病理学和免疫组织化学显示高级别结肠脂肪肉瘤的形态。患者在手术后八个月表现良好,正在接受定期监测。经验教训:原发性胃肠道脂肪肉瘤肿瘤并不常见,结肠变异也极为罕见,尤其是在生命的第二个十年,并且仅限于指尖可以计数的病例报告。阴性边缘的手术切除是唯一的治疗方法。
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 求助全文
来源期刊
自引率
0.00%
发文量
22
审稿时长
24 weeks
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信