Abstract
Superior mesenteric artery syndrome (SMAS), also known as Wilkie’s syndrome, is an exceedingly rare condition concerning intestinal obstruction. SMAS occurs when the space between the superior mesenteric artery (SMA) and the abdominal aorta narrows, resulting in compression of the duodenum. Functionally, the SMA supplies the distal duodenum, two-thirds of the transverse colon, and the pancreas. The location of the SMA is at about the level of the first lumbar vertebra branching off the anterior portion of the abdominal aorta. Generally, SMAS is due to rapid, excessive weight loss, resulting in the loss of the duodenal fat pad. The loss of the fat pad consequently changes the angle between the abdominal aorta and the SMA, or aortomesenteric angle, causing intestinal obstruction. Typical symptoms of acute cases of SMAS include postprandial abdominal pain, nausea, and vomiting; however, chronic cases may present with vague gastrointestinal symptoms and further weight loss. Herein, we discuss the case of a woman with chronic abdominal pain and previous substantial weight loss in whom we note features consistent with SMAS. Several factors can contribute to the syndrome, but, most commonly, it is observed after sudden, significant weight loss accompanied by nonspecific symptoms such as postprandial epigastric pain, emesis, and anorexia. Given that there is continued debate whether the syndrome even exists, SMAS is usually a diagnosis of exclusion, if diagnosed at all. First-line treatment involves conservative management, but if symptoms become too severe, several proven surgical methods are available. SMAS is a rare condition and is difficult to diagnose, but it should be suspected if clinical manifestations are present. This case illustrates the need for primary care physicians to receive additional training on the recognition of rare diseases to broaden their differentials. Training of this sort is especially crucial for rural family medicine residency programs focused on producing full-spectrum physicians.
Highlights
We discuss the case of a middle-aged woman with chronic abdominal pain and previous substantial weight loss in whom we note features consistent with superior mesenteric artery syndrome (SMAS)
SMAS is caused by a compression of the inferior or third part of the duodenum resulting from the narrowing of the space between the superior mesenteric artery (SMA) and the abdominal aorta
Several factors can contribute to the syndrome; most commonly, it is observed after sudden, significant weight loss accompanied by nonspecific symptoms that may include postprandial epigastric pain, emesis, and anorexia
Summary
We discuss the case of a middle-aged woman with chronic abdominal pain and previous substantial weight loss in whom we note features consistent with superior mesenteric artery syndrome (SMAS). She described the pain as constant cramping and wringing, and localized to the left upper and left lower quadrants, and non-radiating, and rated the pain 8 out of 10 on the visual analog pain scale. Chills, hematuria, melena, hematochezia, chest pain, drug abuse, and treatment for mental health issues She reported intermittent symptoms of depression and anxiety due to her recurrent abdominal pain, as well as continued use of opioids for pain management. Due to our patient’s extensive history, additional differentials included post-cholecystectomy syndrome, gastroparesis, idiopathic intestinal pseudo-obstruction, chronic gastritis, and narcotic bowel syndrome [6]
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