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| Discussion |
A
22-year-old man presented with fullness of abdomen associated with intermittent
episodes of vomiting since six months. Except for his asthenic built, there was
no positive physical finding on examination. Routine laboratory investigations
were within normal limits.
RADIOLOGICAL FINDINGS:
An
upper GI series revealed dilatation of the first and second parts of the duodenum
with an abrupt vertical cut off at its third part. The mucosal pattern was normal.
The obstruction to passage of barium was dramatically relieved in the lateral
decubitus position.
Fig.
1 | Fig.
2 |
A contract enhanced CT scan of the abdomen showed a dilated proximal duodenum
with abrupt cut off at its third part. The superior mesenteric artery (SMA) was
seen to pass anterior to the site of the cut off. This was associated with a narrowed
aorta-SMA distance.
Fig.
3 | Fig.
4 . | |
These radiological
findings were interpreted as a manifestation of the superior mesenteric artery
syndrome.
The
patient was operated. Intraoperative findings confirmed the diagnosis of SMA syndrome
as the third part of duodenum was seen to be compressed between the aorta and
SMA. A Roux-en-Y jejunostomy was performed.
DISCUSSION:
The SMA syndrome is an
uncommon, but well recognized, clinical entity characterized by compression of
the third or transverse portion of the duodenum against the aorta by the SMA -
resulting in chronic, intermittent or acute - complete or partial duodenal obstruction.
The SMA syndrome was first described in 1861 by Von Rokitansky, who proposed that
its cause was obstruction of the third part of the duodenum as a result of arteriomesenteric
compression.
Clinical
presentation:
Patients
often present with chronic upper abdominal symptoms such as epigastric pain, nausea,
eructation, voluminous vomiting (bilious or partially digested food), postprandial
discomfort, early satiety, and sometimes - sub acute small-bowel obstruction.
The symptoms are typically relieved when the patient is in the left lateral decubitus,
prone or knee-to-chest position and they are often aggravated when the patient
is in the supine position. An asthenic habitus is noted in about 80% of cases.
Abdominal examination may reveal a succussion splash.
Pathophysiology:
The SMA usually forms an angle of approximately 45° (range, 38-56°)
with the abdominal aorta. The third part of the duodenum crosses caudal to the
origin of the SMA coursing between the SMA and the aorta. Any factor that sharply
narrows the aortomesenteric angle to approximately 6-25° can cause entrapment
and compression of the third part of the duodenum as it passes between the SMA
and the aorta - resulting in the SMA syndrome. In addition, the aortomesenteric
distance in SMA syndrome is decreased to 2-8 mm (normal is 10-20 mm). Alternatively,
other causes implicated in the SMA syndrome include high insertion of the duodenum
at the ligament of Treitz, a low origin of the SMA and compression of the duodenum
due to peritoneal adhesions.
The important etiologic factors that may
precipitate a narrowing of the aortomesenteric angle and result in chronically
recurrent mechanical obstruction include the following:
Imaging Studies:
The diagnosis of SMA syndrome is difficult. Confirmation usually requires radiographic studies such as an upper GI series, hypotonic duodenography and CT scanning.
An uipper GI study with barium reveals characteristic dilatation of the first and second parts of the duodenum with an abrupt vertical or linear cutoff in the third part with normal mucosal folds. Fluoroscopy demonstrates a to-and-fro motion of the barium in the dilated proximal portion of the duodenum. Other findings include a delay of 4-6 hours in gastroduodenal transit and relief of the obstruction when the patient is in the left lateral decubitus position. A Hayes maneuver (i.e. pressure applied below the umbilicus in cephalad and dorsal direction), which elevates the root of small-bowel mesentery may also relieve the obstruction.
CT scanning is useful in the diagnosis of the SMA syndrome and can provide diagnostic information including the aorta-SMA distances and duodenal distension. Also, it can be used to assess intra-abdominal and retroperitoneal fat.
Upper GI endoscopy may be necessary to exclude mechanical causes of duodenal obstruction. However, the diagnosis of SMA syndrome may be missed with this study.
Treatment:
Medical Care: Reversing or removing the precipitating factor is usually successful in a patient with acute SMA syndrome. Conservative initial treatment is recommended in all patients with the SMA syndrome; this includes adequate nutrition, GI decompression, and proper positioning of the patient after eating (i.e. left lateral decubitus, prone, or knee-to-chest position). Surgical Care:
Surgical intervention is indicated when conservative measures are ineffective, particularly in patients with a long history of progressive weight loss, pronounced duodenal dilatation with stasis and complicating peptic ulcer disease. Duodenojejunostomy is the most frequently used procedure and it is successful in about 90% of cases. The use of laparoscopic surgery that involves lysis of the ligament of Treitz and mobilization of the duodenum has also been reported.