A rare cause of upper gastrointestinal system obstruction: Superior mesenteric artery syndrome (Wilkie’s syndrome); two different case reports

IF 0.5 Q4 SURGERY Turkish Journal of Surgery Pub Date : 2024-03-01 DOI:10.47717/turkjsurg.2022.4655
Mehmet Sertkaya, Mehmet Şirik, Mehmet Tepe, S. Özdaş, Mustafa Göksu
{"title":"A rare cause of upper gastrointestinal system obstruction: Superior mesenteric artery syndrome (Wilkie’s syndrome); two different case reports","authors":"Mehmet Sertkaya, Mehmet Şirik, Mehmet Tepe, S. Özdaş, Mustafa Göksu","doi":"10.47717/turkjsurg.2022.4655","DOIUrl":null,"url":null,"abstract":"Superior mesenteric artery syndrome is defined as a collection of clinical symptoms and findings that result from compression of the third part of the duodenum between the aorta and the superior mesenteric artery. Here, we describe two patients who were diagnosed with superior mesenteric artery syndrome. Two patients, 18 and 38 years old, respectively, presented to our clinic with complaints of nausea, vomiting, and weight loss. Computed tomography scans of both patients supported diagnoses of superior mesenteric artery syndrome. The 18-year-old patient recovered with conservative treatment. However, our 38-year-old patient did not recover with conservative treatment and required two surgeries. In the first operation, duodenal release with Treitz’s ligament dissection and pyloroplasty were performed because of concomitant hypertrophic pyloric stenosis. Because the patient exhibited gastroparesis and gastric ptosis after the first operation, subtotal gastrectomy and Roux-n-Y gastrojejunostomy were performed in the second operation. No complications were observed during follow-up after the second operation. Superior mesenteric artery syndrome should be considered in the differential diagnosis of patients with nausea, vomiting, and weight loss of unknown cause. During treatment, weight-gaining conservative approaches should be attempted initially, but surgical treatment should not be excessively delayed in patients who do not respond to medical treatment.","PeriodicalId":23374,"journal":{"name":"Turkish Journal of Surgery","volume":null,"pages":null},"PeriodicalIF":0.5000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Turkish Journal of Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.47717/turkjsurg.2022.4655","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"SURGERY","Score":null,"Total":0}
引用次数: 0

Abstract

Superior mesenteric artery syndrome is defined as a collection of clinical symptoms and findings that result from compression of the third part of the duodenum between the aorta and the superior mesenteric artery. Here, we describe two patients who were diagnosed with superior mesenteric artery syndrome. Two patients, 18 and 38 years old, respectively, presented to our clinic with complaints of nausea, vomiting, and weight loss. Computed tomography scans of both patients supported diagnoses of superior mesenteric artery syndrome. The 18-year-old patient recovered with conservative treatment. However, our 38-year-old patient did not recover with conservative treatment and required two surgeries. In the first operation, duodenal release with Treitz’s ligament dissection and pyloroplasty were performed because of concomitant hypertrophic pyloric stenosis. Because the patient exhibited gastroparesis and gastric ptosis after the first operation, subtotal gastrectomy and Roux-n-Y gastrojejunostomy were performed in the second operation. No complications were observed during follow-up after the second operation. Superior mesenteric artery syndrome should be considered in the differential diagnosis of patients with nausea, vomiting, and weight loss of unknown cause. During treatment, weight-gaining conservative approaches should be attempted initially, but surgical treatment should not be excessively delayed in patients who do not respond to medical treatment.
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
上消化道系统梗阻的罕见病因:肠系膜上动脉综合征(威尔基综合征);两份不同的病例报告
肠系膜上动脉综合征是指主动脉和肠系膜上动脉之间的十二指肠第三部分受到压迫而产生的一系列临床症状和发现。在此,我们描述了两名被诊断为肠系膜上动脉综合征的患者。两名患者分别为 18 岁和 38 岁,因主诉恶心、呕吐和体重减轻来我院就诊。两名患者的计算机断层扫描结果均支持肠系膜上动脉综合征的诊断。18 岁的患者经保守治疗后痊愈。然而,我们的 38 岁患者在接受保守治疗后并未痊愈,而是需要进行两次手术。在第一次手术中,由于合并肥厚性幽门狭窄,患者接受了十二指肠松解术和特雷茨韧带切断术以及幽门成形术。由于患者在第一次手术后出现胃瘫和胃下垂,因此在第二次手术中进行了胃次全切除术和 Roux-n-Y 胃空肠吻合术。第二次手术后的随访中未发现并发症。对于原因不明的恶心、呕吐和体重减轻患者,在鉴别诊断时应考虑肠系膜上动脉综合征。在治疗期间,首先应尝试增加体重的保守治疗方法,但对于药物治疗无效的患者,不应过分拖延手术治疗。
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
1.20
自引率
0.00%
发文量
16
期刊最新文献
FROM THE EDITOR'S DESK. Musinous cystic neoplasia mimicking hydatid cyst in the liver: Two rare cases Comments on ‘Percutaneous gas decompression can ease endoscopic derotation in sigmoid volvulus’ Pathological complete response and associated factors in breast cancer after neoadjuvant chemotherapy: A retrospective study Effect of silver colloid dressing over conventional dressings in diabetic foot ulcer: A prospective study
×
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