The stomach is the site of more than half of gastrointestinal
lymphomas and is the most common organ involved in extranodal lymphomas.
The gastric submucosa does not ordinarily contain lymphoid
tissue, and the development of lymphoid tissue resembling small intestinal Peyer's patches is believed to occur in response to infection with H. pylori.
A number of observations support a causal relationship between
chronic H. pylori infection and lymphoma development. H. pylori is present in the stomachs of more than half of patients with gastric lymphoma.
Low-grade lymphoma is postulated to occur as a result of
monoclonal B-cell proliferation.
B-cell proliferation depends on interleukin-2 production by
antigenically stimulated nonneoplastic T cells.
Complete regression of low-grade MALT lymphomas with
antibiotic treatment has been reported in 70% to 100% of cases. Lymphomas regress in response to H. pylori treatment.
The median time to complete response averaged 5 months.
For disease limited to the mucosa and submucosa, as is the case
in 90% of patients, antibiotics alone are sufficient.
In the rare case of more advanced disease with extension into
the muscularis or serosa, nodal or adjacent organ involvement, disease refractory to antibiotics, or systemic disease, chemotherapy with or without radiotherapy should be considered in addition to H. pylori eradication.
Chemotherapy with cyclophosphamide, doxorubicin, vincristine,
and prednisone (CHOP) with rituximab and 40-50 Gy of radiotherapy is thought to be standard management.