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


SMA syndrome

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:

Symptoms[edit]

The symptoms of SMAS can vary in severity and may include:

Diagnosis[edit]

Diagnosis of SMAS is often challenging due to its rarity and the nonspecific nature of its symptoms. It typically involves:

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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