Gastric Mucosa-Associated Lymphoid Tissue (MALT) Lymphoma

Chapter: Gastric Mucosa-Associated Lymphoid Tissue (MALT) Lymphoma
McMaster Section Editor(s): John K. Marshall
Section Editor(s) in Interna Szczeklika: Witold Bartnik†, Małgorzata Szczepanek
McMaster Author(s): Mohammad Yaghoobi
Author(s) in Interna Szczeklika: Wojciech M. Wysocki, Krzysztof Marlicz†
† Deceased.
Additional Information

Definition, Etiology, PathogenesisTop

Low-grade B-cell lymphoma or extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT) is a non-Hodgkin lymphoma presumably originating from the post–germinal center memory B cells. There are common chromosomal translocations associated with this type of lymphoma, the most frequent ones being t(11;18)(q21;q21) and t(14;18)(q32;q21).

Epidemiology

Stomach is the most common site of gastrointestinal (GI) extranodal lymphomas, accounting for two-thirds of cases. MALT lymphoma and diffuse large B-cell lymphoma (DLBCL) are the two most common types found in the stomach. MALT lymphoma is more frequent in middle-aged patients and accounts for a half of all cases of gastric lymphoma. The overall incidence is estimated to be ~4 in 1,000,000 and involves both men and women equally.

Risk Factors

1. Helicobacter pylori (the most common risk factor).

2. Autoimmune disorders (most commonly Sjögren syndrome and systemic lupus erythematosus).

3. Immune deficiency or immunosuppressive therapy.

4. Celiac disease.

5. Inflammatory bowel disease.

6. Nodular lymphoid hyperplasia.

Clinical FeaturesTop

In most people MALT lymphoma is an incidental finding. The symptoms are very nonspecific and include epigastric pain, weight loss, anorexia, nausea and vomiting, early satiety, or GI bleeding. Occasionally anemia or elevated erythrocyte sedimentation rate may be detected.

DiagnosisTop

Diagnostic Tests

1. Upper endoscopy: Endoscopic assessment with biopsy is the most important diagnostic tool. Findings may include erythema, mass, ulcer, nodularity, and thickened gastric folds. Biopsies should be taken from any abnormal-appearing mucosa as well as the duodenum, gastric antrum, gastric body, and gastroesophageal junction. Endoscopic ultrasonography (EUS) can also play a role in determining the depth of invasion and can be used to obtain core specimens from surrounding enlarged lymph nodes.

The need for confirmation or exclusion of H pylori infection dictates the use of the most sensitive diagnostic strategy. Apart from having a diagnostic value for MALT lymphoma itself, biopsies should be obtained from the normal stomach and examined for the presence of H pylori.

2. Alternative tests, such as the urea breath test, should be used if biopsies are negative for H pylori (effectively performing 2 tests, each with high sensitivity). Genetic testing for t(11;18) identifies tumors that are less likely to transform to high-grade lymphoma or less likely to respond to H pylori eradication therapy. It is important to obtain chest, abdominal, and pelvic computed tomography (CT) scans to exclude distant metastasis.

Differential Diagnosis

DLBCL is the second most common type of lymphoma in the stomach and, given its prognosis, it should always be excluded. The less common types include mantle cell lymphoma, follicular lymphoma, and peripheral T-cell lymphoma.

Staging

The Lugano staging system is used to stage MALT lymphoma and accounts for distant nodal involvement. Stage I and II disease include a single primary lesion or multiple noncontiguous lesions confined to the GI tract that may have nodal involvement. Stage IV (advanced) disease is associated with widespread extranodal involvement or simultaneous supradiaphragmatic nodal involvement.

Screening

At this time there are no defined strategies recommended to screen the general population for MALT lymphoma.

TreatmentTop

Treatment depends on the stage of MALT lymphoma. In nonadvanced disease, which is the most common clinical scenario, eradication of H pylori is the mainstay of treatment. Local guidelines should be applied in choosing the best therapeutic regimen to treat H pylori. It is essential to confirm eradication of H pylori at least 4 weeks after completion of an eradication regimen. It is also key to avoid proton pump inhibitors for ≥1 week (or 2 weeks if well tolerated by the patient) before the confirmation test to prevent false-negative results, as the use of PPIs decreases test sensitivity (sensitivity difference of 3%-4% between 1 and 2 weeks of PPI abstinence).Evidence 1Moderate Quality of Evidence (moderate confidence that we know true effects of the intervention). Quality of Evidence lowered due to indirectness. Laine L, Estrada R, Trujillo M, Knigge K, Fennerty MB. Effect of proton-pump inhibitor therapy on diagnostic testing for Helicobacter pylori. Ann Intern Med. 1998 Oct 1;129(7):547-50. PubMed PMID: 9758575. It is not uncommon for H pylori to require a second or third line of treatment to achieve eradication. The preferred test for confirming eradication is the urea breath test or endoscopic biopsy. Serology should not be used for this purpose. Also see Peptic Ulcer Disease.

If eradication is confirmed, surveillance endoscopies are required to monitor tumor response. It is crucial to exclude more advanced lymphomas, such as DLBCL. If the disease persists despite H pylori eradication, localized radiotherapy is the next universally accepted therapeutic option. Those with stage IV MALT lymphoma may require rituximab or chemotherapy.

Patients without H pylori infection do not require eradication treatment and should receive localized radiotherapy as the first line of treatment.

PrognosisTop

Prognosis is generally good, with the 5-year survival rate >90%.

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