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Radiological Case of the Month
Phyllis R. Bishop, MD;
Michael J. Nowicki, MD;
Paul H. Parker, MD
From the Department of Pediatrics, Division of Pediatric Gastroenterology
and Nutrition, Blair E. Batson Children's Hospital, University of Mississippi
Medical Center, Jackson.
Arch Pediatr Adolesc Med. 2001;155:413-414.
A 3-YEAR-OLD boy was referred to the pediatric gastroenterology department
for evaluation of abdominal pain and vomiting. The patient had a 1-year history
of recurrent, acute, episodic abdominal pain that was often associated with
vomiting. The episodes occurred infrequently and typically lasted for 48 to
72 hours. There was no nocturnal awakening with abdominal pain or emesis.
There was no associated fever, diarrhea, rash, headache, or altered consciousness.
The child has maintained growth at the 25th percentile both for height and
weight.
Findings from physical examination were normal except for the abdomen.
Mild abdominal distension was present with a sense of fullness to palpation,
but no mass was felt. There was no tenderness to deep palpation. Results of
rectal examination were normal, and a stool sample was guaiac negative. The
following laboratory studies were performed and revealed normal results: complete
blood cell count, erythrocyte sedimentation rate, amylase, lipase, urinalysis,
and urine culture. An abdominal computed tomographic scan was obtained (Figure 1). Surgery was performed,
and a large cystic mass was removed (Figure
2).
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Figure 1.
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Figure 2.
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Denouement and Discussion: Mesenteric Cyst
Figure 1. An abdominal computed tomographic scan revealed a large cystic mass
displacing the bowel superiorly.
Figure 2. Surgically resected specimen revealing a thin-walled, bilobed cyst
containing clear amber fluid.
Based on the findings of the abdominal computed tomographic scan, surgery
was planned. A large, bilobed mesenteric cyst was found, involving the ileum.
The cyst was removed, and segmental intestinal resection with primary anastomosis
was necessary. The pathologist identified the cyst as a cystic lymphangioma
of the mesentery.
Mesenteric cysts are rare, benign, intra-abdominal tumors, and fewer
than 1000 cases are reported since Benevieni's original description in 1505.1, 2 One third of reported cases involve
children younger than age 10 years.3, 4
The incidence of mesenteric cysts in children ranges from 1 per 11 250
to 1 per 34 000 hospitalizations.2, 5
Most are considered congenital in origin. Proposed mechanisms of development
include sequestration or obstruction of lymphatic vessels and ectopic lymphatic
tissue.6, 7, 8
Mesenteric cysts may arise from trauma, infection, or neoplasm.6
They are grouped with omental and retroperitoneal cysts because of a common
origin and histologic features.9
Mesenteric cysts are described in the mesentery from the duodenum to
the rectum; however, half are found in the small intestine mesentery, usually
near the ileum.2, 4, 5, 9
The patterns of presentation include specific abdominal signs and the incidental
finding of an abdominal mass.10 Presentation
relates to size, location, and associated complications. Most children with
mesenteric cysts are symptomatic; only 20% of mesenteric cysts in children
are asymptomatic.2 A palpable mass is found
on physical examination in 30% to 50% of affected children.2, 3, 9, 11
Occasionally, these patients are surgical emergencies, particularly when there
is intestinal obstruction or appendicitis.9, 12
Other presentations include acute abdomen due to hemorrhage, rupture, or torsion
of the cyst, which may predispose to volvulus with resultant intestinal infarction.13, 14
Diagnosis is not made by history, clinical features, or findings from
laboratory examination; radiological evaluation is necessary. Findings from
abdominal radiographs are normal or show bowel displacement by the mass. Sometimes
calcifications are seen in the cyst wall. The more useful modalities that
demonstrate the cystic nature of the mass are abdominal ultrasound or computed
tomographic scan.10
The treatment of choice for mesenteric cysts is complete surgical excision.
In 33% to 60% of children with mesenteric cysts, segmental bowel resection
is required to fully excise the cyst.2, 3, 5
Although the greatest experience is with open surgery, laparoscopic surgery
has been used.15, 16 Marsupialization
is performed in approximately 10% of the cases.2, 5
Neither partial resection nor cyst aspiration is adequate treatment, and both
result in a high recurrence rate, while patients with total excision have
a negligible risk of recurrence.
AUTHOR INFORMATION
Accepted for publication February 24, 1999.
Reprints: Phyllis R. Bishop, MD, Department of Pediatrics, Division
of Pediatric Gastroenterology and Nutrition, Blair E. Batson Children's Hospital,
University of Mississippi Medical Center, Jackson, MS 39216.
REFERENCES
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1. Swartley WR. Mesenteric cysts. Ann Surg. 1997;85:886-896.
2. Egozi El, Ricketts RR. Mesenteric and omental cysts in children. Am Surg. 1997;63:287-290.
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cyst was present. Arch Surg. 1950;60:699-706.
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13. Namasivayam J, Ziervogel MA, Hollman AS. Case report: volvulus of a mesenteric cyst: an unusual complication
diagnosed by CT. Clin Radiol. 1992;46:211-212.
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14. Wong SW, Gardner V. Sudden death in children due to mesenteric defect and mesenteric cyst. Am J Forensic Med Pathol. 1992;13:214-216.
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15. Shimura H, Ueda J, Ogawa Y, Ichimiya H, Tanaka M. Total excision of mesenteric cysts by laproscopic surgery: report of
two cases. Surg Laparosc Endosc. 1997;7:173-176.
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16. Brentano L, Faccini P, de Castro Oderich GS. Laparoscopic resection of a mesenteric cyst. Surg Laparosc Endosc. 1998;8:402-403.
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SECTION EDITOR: BEVERLY P. WOOD, MD
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