Superior mesenteric artery syndrome: Diagnosis and management

• Published in: World journal of clinical cases 2023-05, Vol.11 (15), p.3369-3384
• Main Authors: Oka, Akihiko, Awoniyi, Muyiwa, Hasegawa, Nobuaki, Yoshida, Yuri, Tobita, Hiroshi, Ishimura, Norihisa, Ishihara, Shunji
• Format: Article
• Language: English
• Subjects: Review
• ISSN: 2307-8960; 2307-8960
• DOI: 10.12998/wjcc.v11.i15.3369

Superior mesenteric artery (SMA) syndrome (also known as Wilkie's syndrome, cast syndrome, or aorto-mesenteric compass syndrome) is an obstruction of the duodenum caused by extrinsic compression between the SMA and the aorta. The median age of patients is 23 years old (range 0-91 years old) and predominant in females over males with a ratio of 3:2. The symptoms are variable, consisting of postprandial abdominal pain, nausea and vomiting, early satiety, anorexia, and weight loss and can mimic anorexia nervosa or functional dyspepsia. Because recurrent vomiting leads to aspiration pneumonia or respiratory depression via metabolic alkalosis, early diagnosis is required. The useful diagnostic modalities are computed tomography as a standard tool and ultrasonography, which has advantages in safety and capability of real-time assessments of SMA mobility and duodenum passage. The initial treatment is usually conservative, including postural change, gastroduodenal decompression, and nutrient management (success rates: 70%-80%). If conservative therapy fails, surgical treatment ( ., laparoscopic duodenojejunostomy) is recommended (success rates: 80%-100%).