AJR:182, June 2004 1463
Original Report
OBJECTIVE. This study was undertaken to describe the CT features of primary gastrointesti-
nal stromal tumors in the omentum and mesentery and to identify any pathologic correlation.
CONCLUSION. On contrast-enhanced CT, primary gastrointestinal stromal tumors in
the omentum and mesentery are usually well-defined, huge masses that contain large areas of
low-attenuation necrosis and hemorrhage and that lack central gas.
astrointestinal stromal tumors ac-
count for most primary mesenchy-
mal tumors of the gastrointestinal
tract [1]. Older articles in the medical literature
refer to these tumors as leiomyomas, leiomyo-
blastomas, and leiomyosarcomas, because
these tumors were believed to originate from
the smooth-muscle layers of the gastrointesti-
nal tract wall. Recently, immunoreactivity for
KIT (CD117, a tyrosine kinase growth factor
receptor) has allowed gastrointestinal stromal
tumors to be distinguished from true leiomyo-
mas, leiomyosarcomas, neurofibromas, and
schwannomas [2]. Moreover, the recent avail-
ability of the KIT tyrosine kinase inhibitor
(STI-571, imatinib [Gleevec], Novartis) has
revolutionized the treatment of gastrointestinal
stromal tumors [3], which makes it important
to know this disease entity.
Gastrointestinal stromal tumors are most
frequently found in the stomach (60–70%),
followed by the small intestine (20–30%), col-
orectum (10%), and esophagus (< 5%) [4]. Al-
though stromal tumors in the gastrointestinal
tract commonly metastasize to the omentum
and mesentery, they may also occur as primary
tumors outside the gastrointestinal tract, espe-
cially in the omentum and the mesentery [5]. A
number of studies of gastrointestinal stromal
tumors have been published in the radiology
literature [6–9]; however, few case reports are
available on the imaging appearances of pri-
mary gastrointestinal stromal tumors in the
omentum and mesentery [10, 11]. The purpose
of our study was to describe the CT findings of
primary gastrointestinal stromal tumors in the
omentum and mesentery and to identify any
pathologic correlation.
Materials and Methods
From January 1999 to May 2003, eight primary
gastrointestinal stromal tumors in the omentum and
mesentery were registered at the pathology registry of
our institution. None of these tumors involved the gas-
tric or intestinal walls, and no patient had a previous
history of gastrointestinal stromal tumors. Clinical data
were reviewed for patient age, sex, and presenting
symptoms. The institutional review board at our hospi-
tal did not require approval or informed patient con-
sent for the review of medical records and images.
CT data were available on a PACS (picture ar-
chiving and communications system, Marotech) in all
patients. CT examinations were performed with a So-
matom Plus-4 (Siemens Medical Solutions) or a Hi-
Speed Advantage (General Electric Medical Systems)
scanner. Each patient received 120 mL of nonionic
contrast material ([iopromide] Ultravist 370, Scher-
ing) through an 18-gauge angiographic catheter in-
serted into a forearm vein. The contrast material was
Hyo-Cheol Kim
1
Jeong M in Lee
1
Se Hyung Kim
1
Kyoung Won Kim
2
Minjin Lee
3
Young Jun Kim
1
Joon Koo Han
1
Byung Ihn Choi
1
Received September 26, 2003; accepted after revision
November 20, 2003.
Supported in part by a grant from the 2003 BK21 Project for
Medicine, Dentistry, and Pharmacy.
1
Department of Radiology, Seoul National University
College of Medicine, Institute of Radiation Medicine,
SNUMRC, and Clinical Research Institute, Seoul National
University Hospital, 28 Yongon-dong, Chongno-gu, Seoul
110-744, Korea. Address correspondence to J. M. Lee
(leejm@radcom.snu.ac.kr).
2
Department of Radiology, Asan Medical Center, University
of Ulsan College of Medicine, Seoul, Korea.
3
Department of Pathology, Seoul National University
College of Medicine, Seoul National University Hospital,
Seoul, Korea.
AJR 2004;182:1463–1467
0361–803X/04/1826–1463
© American Roentgen Ray Society
G
Primary Gastrointestinal Stromal
Tumors in the Omentum and
Mesentery: CT Findings and Pathologic
Correlations
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