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   » » Wiki: Gastric Lymphoma
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Primary gastric lymphoma ( that originates in the stomach itself) is an uncommon condition, accounting for less than 15% of gastric malignancies and about 2% of all lymphomas. However, the stomach is a very common extranodal site for lymphomas (lymphomas originate elsewhere and to the stomach). It is also the most common source of lymphomas in the gastrointestinal tract.


Signs and symptoms
Symptoms include pain, early satiety, fatigue and weight loss. Most people affected by primary gastric lymphoma are over 60 years old.


Risk factors
Risk factors for gastric lymphoma include the following:
  • Helicobacter pylori
  • Long-term immunosuppressant drug therapy
  • infection


Pathophysiology
The majority of gastric lymphomas are non-Hodgkin's lymphoma of origin. These tumors may range from well-differentiated, superficial involvements (MALT) to high-grade, large-cell lymphomas. Sometimes, it's hard to differentiate poorly differentiated high grade B-cell gastric lymphoma from gastric adenocarcinoma clinically or radiologically, yet histopathology with immunohistochemistry is recommended to stain specific markers on the malignant cell that favor the diagnosis of lymphoma. Immunohistochemistry stains specific clusters of differentiation that are present on B-cells like CD20. is also a surface marker that is presented on epithelial cells, is stained histochemically and favors the diagnosis of epithelial tumors like adenocarcinoma.

Distinguishing poorly differentiated gastric lymphoma from adenocarcinoma is essential because the prognosis and modalities of treatment differ significantly.

Other lymphomas involving the stomach include mantle cell lymphoma and which may be associated with ; the latter usually occur in the but have been reported in the stomach.


Diagnosis
These lymphomas are difficult to differentiate from gastric adenocarcinoma. The lesions are usually ulcers with a ragged, thickened pattern on contrast radiographs.

The diagnosis is typically made by at the time of . Several endoscopic findings have been reported, including solitary ulcers, thickened gastric folds, mass lesions and nodules. As there may be infiltration of the submucosa, larger , endoscopic ultrasound guided biopsy, endoscopic submucosal resection, or may be required to obtain tissue.

Imaging investigations including CT scans or endoscopic ultrasound are useful to stage disease. Hematological parameters are usually checked to assist with staging and to exclude concomitant . An elevated LDH level may be suggestive of lymphoma.


Treatment
Diffuse large B-cell lymphomas of the stomach are primarily treated with with CHOP (cyclophosphamide+doxorubicine+vincristine+prednisone) with or without being a usual first choice.

Antibiotic treatment to eradicate H. pylori is indicated as first line therapy for . About 80% of MALT lymphomas completely regress with eradication therapy. Radiation treatment for H. pylori–negative gastric malt lymphoma, has a high success rate, 90% or better after 5 years. Second line therapy for MALT lymphomas is usually chemotherapy with a single agent, and complete response rates of greater than 70% have been reported.

Subtotal , with post-operative is undertaken in refractory cases, or in the setting of complications, including gastric outlet obstruction.


See also
  • Lymphoepithelial lesion

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