Mesenchymal tumors are a heterogeneous group of intramural lesions that arise deep to the mucosa.
1.4 Mesenchymal Tumors
CLINICAL FEATURES
• Mesenchymal tumors are a heterogeneous group of intramural lesions that arise deep to the mucosa.
• Gastrointestinal stromal tumor (GIST) accounts for the majority of solid mesenchymal neoplasms; these tumors arise from the interstitial cells of Cajal (GI pacemaker cells).
• Other mesenchymal tumors include smooth muscle tumors (e.g., leiomyoma), neurogenic tumors (e.g., schwannoma, neurofibroma), vascular tumors (e.g., hemangioma), and hamartomas.
• GISTs were previously misclassified as smooth muscle tumors.
• Mesenchymal tumors may present with acute or occult GI bleeding secondary to ulceration of the overlying mucosa.
• Malignant mesenchymal tumors typically spread via direct local extension, intraperitoneal seeding, or hematogenously (to liver).
• Small bowel lipomas are generally benign incidental findings but may lead to intussusception.
• Hamartomas consist of varying amounts of smooth muscle and epithelial tissue.
• Multiple small bowel hamartomas are a common finding in Peutz-Jeghers syndrome; these benign polyps may act as lead points for intussusception.
• Hemangiomas and lymphangiomas of the small bowel are usually asymptomatic incidental findings; see section 3.9 for discussion of vascular ectasia.
• Most nerve sheath tumors (i.e., schwannomas and neurofibromas) are benign.
IMAGING FEATURES
• Mesenchymal tumors are intramural masses that typically manifest as smooth, broad-based impressions on barium studies; nonulcerated lesions may be difficult to distinguish from extrinsic impression.
• CT and MR are useful for demonstrating both the intramural and exoenteric tumor components, which are typically much more prominent than the endoluminal component.
• CT can evaluate for metastatic disease and monitor response to therapy (which is often striking in cases of GIST).
• A densely calcified lesion is suggestive of a leiomyoma.
• CT can provide an imaging-specific diagnosis for lipomas, obviating tissue sampling.
• Hemangiomas are typically small but can present as large polypoid lesions; the presence of phleboliths may allow for a specific diagnosis.
• Lymphangiomas may present as a polypoid or lobulated submucosal lesion and may be pliable at fluoroscopy and endoscopy; most will appear cystic on cross-sectional imaging.
FIGURES
Figure 1.4.1 Small bowel GIST.
Figure 1.4.2 Ulcerated small bowel GIST.
Figure 1.4.3 Small bowel lipomas.
Figure 1.4.4 Small bowel hamartomas.
Figure 1.4.5 Peutz-Jeghers syndrome.
Copyright © 2007 by Saunders, an imprint of Elsevier, Inc.
















![Images show the pectoralis muscles of a healthy male individual who never smoked (age, 66 years; height, 178 cm; body mass index [BMI, calculated as weight in kilograms divided by height in meters squared], 28.4; number of cigarette pack-years, 0; forced expiratory volume in 1 second [FEV1], 97.6% predicted; FEV1: forced vital capacity [FVC] ratio, 0.71; pectoralis muscle area [PMA], 59.4 cm2; pectoralis muscle volume [PMV], 764 cm3) and a male individual with a smoking history and chronic obstructive pulmonary disorder (COPD) (age, 66 years; height, 178 cm; BMI, 27.5; number of cigarette pack-years, 43.2, FEV1, 48% predicted; FEV1:FVC, 0.56; PMA, 35 cm2; PMV, 480.8 cm3) from the Canadian Cohort Obstructive Lung Disease (i.e., CanCOLD) study. The CT image is shown in the axial plane. The PMV is automatically extracted using the developed deep learning model and overlayed onto the lungs for visual clarity.](https://img.auntminnie.com/mindful/smg/workspaces/default/uploads/2026/03/genkin.25LqljVF0y.jpg?auto=format%2Ccompress&crop=focalpoint&fit=crop&h=112&q=70&w=112)



