Superior mesenteric artery syndrome

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| Superior mesenteric artery syndrome | |
|---|---|
| Synonyms | Wilkie's syndrome, cast syndrome |
| Pronounce | |
| Specialty | Gastroenterology, Vascular surgery |
| Symptoms | Abdominal pain, nausea, vomiting, early satiety, weight loss |
| Complications | Malnutrition, dehydration, electrolyte imbalance |
| Onset | Typically adolescence or young adulthood |
| Duration | Variable |
| Types | N/A |
| Causes | Anatomical compression of the duodenum |
| Risks | Rapid weight loss, spinal surgery, congenital anatomical variations |
| Diagnosis | Clinical evaluation, imaging studies such as CT scan, barium swallow |
| Differential diagnosis | Peptic ulcer disease, pancreatitis, gastroesophageal reflux disease |
| Prevention | N/A |
| Treatment | Nutritional support, surgical intervention such as duodenojejunostomy |
| Medication | Prokinetics, antiemetics |
| Prognosis | Generally good with treatment |
| Frequency | Rare |
| Deaths | Rare |
A rare digestive system disorder

Superior mesenteric artery syndrome (SMAS) is a rare, potentially life-threatening gastrointestinal disorder characterized by the compression of the duodenum between the abdominal aorta and the superior mesenteric artery (SMA). This condition leads to partial or complete blockage of the duodenum, resulting in a variety of gastrointestinal symptoms.
Pathophysiology[edit]
The superior mesenteric artery arises from the anterior surface of the abdominal aorta and supplies blood to a large portion of the intestines. In SMAS, the angle between the SMA and the aorta is reduced, typically to less than 25 degrees, compared to the normal range of 38-56 degrees. This narrowing can compress the third part of the duodenum, leading to obstruction.
Causes[edit]
SMAS can be caused by any condition that results in a loss of the mesenteric fat pad, which normally acts as a cushion between the SMA and the duodenum. Common causes include:
- Significant weight loss due to anorexia nervosa, malignancy, or malabsorption syndromes.
- Congenital anatomical abnormalities.
- Surgical procedures that alter the position of the SMA or duodenum.
Symptoms[edit]
The symptoms of SMAS can vary in severity and may include:
- Severe abdominal pain
- Nausea and vomiting
- Early satiety
- Bloating
- Weight loss
- Postprandial fullness
Diagnosis[edit]
Diagnosis of SMAS is often challenging due to its rarity and the nonspecific nature of its symptoms. It typically involves:
- Upper gastrointestinal series
- Computed tomography (CT) scan
- Magnetic resonance imaging (MRI)
- Doppler ultrasound to assess blood flow and the angle between the SMA and aorta.
Treatment[edit]
Treatment of SMAS focuses on relieving the duodenal obstruction and addressing the underlying cause. Options include:
- Nutritional support to restore weight and the mesenteric fat pad.
- Postural therapy, such as lying in the left lateral decubitus or prone position to relieve compression.
- Surgical intervention, such as duodenojejunostomy or gastrojejunostomy, in severe cases where conservative measures fail.
Prognosis[edit]
The prognosis for SMAS varies depending on the severity of the condition and the success of treatment. With appropriate management, many patients experience significant improvement in symptoms.
See also[edit]
External links[edit]
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