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Recent advances upper gastrointestinal lymphomas: molecular updates and diagnostic implications
Periklis G Foukas1, Bettina Bisig2, Laurence de Leval1
1Second Department of Pathology, National and Kapodistrian University of Athens, Attikon University Hospital, Athens, Greece.
Gastrointestinal lymphomas, common in the stomach and small intestine, are often diffuse large B-cell lymphoma or extranodal marginal zone lymphoma. Advances in molecular pathology are crucial for diagnosing these upper GI lymphoproliferative diseases.
Area of Science:
- Gastroenterology
- Hematology
- Oncology
Background:
- Extranodal non-Hodgkin lymphomas frequently involve the gastrointestinal tract, primarily the stomach, duodenum, and proximal small intestine.
- Diffuse large B-cell lymphoma and extranodal marginal zone lymphoma are the most common types.
- Systemic lymphomas can also manifest in or spread to the GI tract.
Purpose of the Study:
- To provide an update on recent developments in the pathology and molecular pathology of upper gastrointestinal lymphoproliferative diseases.
- To highlight the evolving classification and diagnostic approaches for primary GI T-cell neoplasms and aggressive B-cell tumors.
- To emphasize the integration of molecular genetic markers alongside morphology and immunophenotype.
Main Methods:
- Review of current literature on gastrointestinal lymphomas.
- Analysis of recent advances in molecular pathology and classification of lymphoid neoplasms.
- Consideration of endoscopic and clinical presentations in diagnosis.
Main Results:
- Significant changes in the classification of primary GI T-cell neoplasms.
- Increased importance of molecular genetic markers in diagnosing aggressive B-cell tumors.
- Recognition of diverse presentations of GI lymphoproliferative diseases.
Conclusions:
- Accurate diagnosis of upper GI lymphoproliferative diseases requires a multimodal approach.
- Molecular pathology plays an increasingly vital role in refining diagnoses and classifications.
- Understanding the interplay of morphology, immunophenotype, molecular markers, and clinical presentation is essential.
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