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Updated: Mar 26, 2026

Establishment and Characterization of Small Bowel Neuroendocrine Tumor Spheroids
Published on: October 14, 2019
Pathology of Gastrointestinal Neuroendocrine Tumors: An Update
Roger K Moreira1, Kay Washington2
1Department of Pathology, Columbia University Medical Center, 630 West 168th Street, New York, NY 20032, USA.
Abstract:
Gastrointestinal (GI) neuroendocrine tumors (NETs) are a heterogeneous group of relatively slow-growing neoplasms with marked site-specific differences in hormonal secretion and clinical behavior. Most are sporadic neoplasms, with only 5% to 10% arising in patients with hereditary disorders, most commonly in multiple endocrine neoplasia type 1. Although a uniform terminology is not universally accepted, use of the 4-category WHO classification of these tumors is becoming more widespread, and recommendations for tumor grading and staging have been recently formulated. Most GI NETs are easily recognized on routine histologic examination; rarely, a limited panel of immunohistochemical markers may be useful in establishing the diagnosis. This article describes general and site-specific features of these tumors and outlines potential pitfalls in diagnosis.
Insights
Gastrointestinal neuroendocrine tumors (GI NETs) are diverse neoplasms with varying behaviors. This review covers their classification, grading, staging, and diagnostic considerations.
Area of Science:
- Gastroenterology and Oncology
- Pathology
- Endocrinology
Background:
- Gastrointestinal neuroendocrine tumors (GI NETs) are a heterogeneous group of neoplasms.
- Most GI NETs are sporadic, with a minority linked to hereditary conditions like multiple endocrine neoplasia type 1.
- Tumor behavior and hormonal secretion vary significantly based on tumor site.
Purpose of the Study:
- To provide a comprehensive overview of gastrointestinal neuroendocrine tumors.
- To discuss the evolving WHO classification, grading, and staging recommendations for GI NETs.
- To highlight diagnostic challenges and potential pitfalls in identifying these tumors.
Main Methods:
- Review of current literature on GI NETs.
- Discussion of histopathological features and diagnostic markers.
- Analysis of site-specific characteristics and clinical behaviors.
Main Results:
- GI NETs exhibit significant heterogeneity in hormonal secretion and clinical presentation.
- A 4-category WHO classification is increasingly adopted for GI NETs.
- Histologic examination is typically sufficient for diagnosis, with immunohistochemistry used in select cases.
Conclusions:
- Accurate classification, grading, and staging are crucial for managing GI NETs.
- Understanding site-specific features aids in diagnosis and treatment planning.
- Awareness of diagnostic pitfalls is essential for optimal patient care.
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