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Gastrointestinal Stromal Tumors and Other
Mesenchymal Lesions of the Gut
Joel K. Greenson, M.D.
Department of Pathology, University of Michigan Health System, Ann Arbor, Michigan
Although a great many mesenchymal lesions may be
In the past 5 years, there has been a paradigm shift found in the gastrointestinal (GI) tract, none are more
in our understanding of gastrointestinal stromal tu- vexing to the surgical pathologist than stromal tu-
mors (GISTs). Once thought to be smooth muscle mors. In 1960, Martin and colleagues (1) published a
tumors, these uncommon neoplasms are now series of six cases of “intramural myoid tumors” of the
thought to differentiate along the lines of interstitial stomach and theorized that these unusual tumors
cells of Cajal, the pacemaker cells of the gut. Along were of smooth muscle origin. Two years later, Stout
with this understanding comes an exciting new (2) introduced the term leiomyoblastoma to describe
drug therapy (Gleevec) that for the first time offers a group of bizarre smooth muscle tumors of the stom-
real hope to patients with malignant stromal tu- ach. Since that time, a wide variety of names have
mors. Overall, approximately 60–70% of stromal been used to describe these spindle and epithelioid
tumors are from the stomach, 20–30% are from the cell tumors that may arise anywhere along the GI tract
small intestine, and 10% come from the esopha- as well as in the omentum and mesentery. In 1983,
gus, colon, rectum, omentum, and mesentery. Be- Mazur and Clark (3) first used the term stromal tumor
tween 10 and 30% of GISTs are malignant. Stromal to describe
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