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Updated: Aug 11, 2026

In vitro Organoid Culture of Primary Mouse Colon Tumors
Published on: May 17, 2013
Tumors of the appendix and colon
K F Hatch1, D K Blanchard, G F Hatch
1Centers for Surgical Anatomy and Technique, Emory University School of Medicine, 1462 Clifton Road, NE, Suite 303, Atlanta, Georgia 30322, USA.
This review analyzes smooth muscle tumors of the large intestine, including leiomyomas (LMs) and leiomyosarcomas (LMSs). Leiomyosarcomas were more common in older males and grew within the lumen, unlike leiomyomas.
Area of Science:
- Gastroenterology
- Surgical Pathology
- Oncology
Background:
- Smooth muscle tumors of the appendix and large intestine are rare.
- Comprehensive data on these tumors, including benign leiomyomas (LMs) and malignant leiomyosarcomas (LMSs), are limited.
- A review of global literature is needed to consolidate existing knowledge.
Purpose of the Study:
- To conduct a collective review of all reported cases of smooth muscle tumors of the appendix and large intestine.
- To analyze cumulative and recent data on both benign and malignant smooth muscle tumors from 1875 to 1996.
- To characterize the epidemiology, clinical presentation, and pathological features of these tumors.
Main Methods:
- Systematic literature search for case reports of smooth muscle tumors in the appendix and large intestine.
- Inclusion of all available case reports from 1875 to 1996.
- Data extraction and analysis of tumor incidence, demographics, location, growth patterns, symptoms, and metastasis.
Main Results:
- A total of 331 leiomyomas (LMs) and 263 leiomyosarcomas (LMSs) were reported.
- Peak incidence for LMs was ages 30-39; for LMSs, ages 50-59.
- Descending and sigmoid colon were most common sites; LMs grew extraluminally, LMSs intraluminally.
- Pain was the most frequent symptom for both; LMSs were larger and metastasized more frequently.
Conclusions:
- Smooth muscle tumors of the large intestine exhibit distinct demographic and clinical characteristics.
- Leiomyosarcomas present a greater diagnostic and therapeutic challenge due to their size, intraluminal growth, and metastatic potential.
- Further research into the pathogenesis and management of these rare tumors is warranted.
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