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一例肠系膜上动脉综合征。

A case of superior mesenteric artery syndrome.

作者信息

Rao Shiavax J, Lakra Pallavi, Paudel Kalyan, Haas Christopher J

机构信息

Department of Medicine, MedStar Union Memorial Hospital, MedStar Health Internal Medicine Residency Program, Baltimore, MD, USA.

Department of Radiology, MedStar Harbor Hospital, Baltimore, MD, USA.

出版信息

Radiol Case Rep. 2022 Apr 21;17(6):2235-2237. doi: 10.1016/j.radcr.2022.03.090. eCollection 2022 Jun.

Abstract

Superior mesenteric artery (SMA) syndrome, also known as Cast syndrome, Wilkie's syndrome, or duodenal ileus, is a rare condition involving compression of the duodenum between the aorta and the SMA, primarily attributed to loss of the intervening mesenteric fat pad. Clinical symptoms include postprandial epigastric abdominal pain, nausea, emesis, and weight loss. At-risk individuals include those with rapid weight loss, debilitating illness, malignancy, malabsorption syndromes, trauma, neurologic injury, eating disorders, and substance abuse. Here, we present a case of SMA syndrome in a 24-year-old woman presenting with nausea, vomiting, and abdominal pain who improved with conservative management.

摘要

肠系膜上动脉(SMA)综合征,也称为卡斯综合征、威尔基综合征或十二指肠梗阻,是一种罕见的疾病,主要由于肠系膜脂肪垫消失,导致十二指肠在主动脉和肠系膜上动脉之间受到压迫。临床症状包括餐后上腹部疼痛、恶心、呕吐和体重减轻。高危人群包括体重快速下降、患有消耗性疾病、恶性肿瘤、吸收不良综合征、创伤、神经损伤、饮食失调和药物滥用的患者。在此,我们报告一例24岁女性的肠系膜上动脉综合征病例,该患者表现为恶心、呕吐和腹痛,经保守治疗后病情好转。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bc0/9046803/89470c8fa7de/gr1.jpg

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