Superior mesenteric artery syndrome (SMAS) is a rare condition. The di
agnosis is usually made by exclusion. A previously healthy 20-year-old
woman who had recurrent SMAS is described. Diagnosis of the condition
was difficult. Initially, small-bowel enteroclysis, upper gastrointes
tinal series and endoscopy, biopsy of gastric and duodenal mucosa, abd
ominal computed tomography (CT) and ultrasonography were used to make
the diagnosis. Abdominal CT suggested pancreatitis causing compressive
obstruction of the superior mesenteric artery. Conservative managemen
t was helpful at first, but cramping and projectile emesis recurred. U
pper gastrointestinal series suggested duodenal distension and a filli
ng defect in the region of the superior mesenteric artery. Repeat endo
scopy showed a lateral pulsatile compression in the region of the dist
al duodenum and SMAS was diagnosed. Medical therapy was not helpful so
duodenojejunostomy was carried out. The operation was successful and
the patient was symptom-free for 1 year, when the syndrome recurred, w
ith symptoms of periumbilical pain, intermittent episodes of vomiting
and loose stools. At reoperation the duodenojejunal anastomosis was fo
und to be displaced to the left of the superior mesenteric artery pedi
cle causing recurrent obstruction. The duodenojejunostomy was converte
d to a Roux-en-Y duodenojejunostomy. The patient has since remained we
ll. A MEDLINE search of the literature for the period 1961 to October
1994 revealed that there were no reported cases of a recurrence of SMA
S in an otherwise healthy adult patient. In spite of the difficulty in
diagnosing this condition, heightened awareness can lead to early dia
gnosis and avoid unnecessary suffering for the patient.