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Logo of gutliverThis ArticleAims and ScopeInstructions to AuthorsE-SubmissionGut and Liver
 
Gut Liver. Apr 2012; 6(2): 270–274.
Published online Apr 17, 2012. doi:  10.5009/gnl.2012.6.2.270
PMCID: PMC3343168
Regression of Advanced Gastric MALT Lymphoma after the Eradication of Helicobacter pylori
Soo-Kyung Park, Hwoon-Yong Jung,corresponding author Do Hoon Kim, Mi-Young Kim, Jeong Hoon Lee, Kwi Sook Choi, Kee Don Choi, Ho June Song, Gin Hyug Lee, and Ho Kim
Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
corresponding authorCorresponding author.
Correspondence to: Hwoon-Yong Jung. Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul 138-736, Korea. Tel: +82-2-3010-3180, Fax: +82-2-476-0824, hwoonymd/at/gmail.com
Received July 31, 2010; Revised September 28, 2010; Accepted October 11, 2010.
A 66-year-old female presented with a 1-month history of dyspepsia. An initial upper gastrointestinal endoscopy with biopsy revealed a low-grade mucosa-associated lymphoid tissue (MALT) lymphoma. A rapid urease test was positive for Helicobacter pylori. Endoscopic ultrasound (EUS) and computed tomography (CT) revealed a 30×15-mm lymph node (LN) in the subcarinal area. Histopathologic and phenotypic analyses of the biopsy specimens obtained by EUS-guided fine-needle aspiration revealed a MALT lymphoma, and the patient was diagnosed with a stage 4E gastric MALT lymphoma. One year after H. pylori eradication, the lesion had disappeared, as demonstrated by endoscopy with biopsy, CT, fusion whole-body positron emission tomography, and EUS. Here, we describe a patient with gastric MALT lymphoma that metastasized to the mediastinal LN and regressed following H. pylori eradication.
Keywords: Marginal zone B-cell lymphoma, Stomach
INTRODUCTION
The most common primary lymphoma of the gastrointestinal (GI) tract is mucosa-associated lymphoid tissue (MALT) lymphoma.1 Although 90% of gastric MALT lymphomas are related to the presence of Helicobacter pylori,2 areas other than the GI tract may be affected. We describe here a patient with gastric MALT lymphoma that metastasized to the mediastinal lymph node (LN) and regressed following H. pylori eradication.
A 66-year-old female presented with a 1-month history of dyspepsia. An initial upper GI endoscopy showed a shallow ulcerative lesion in the gastric high body and a hyperemic lesion in the low body (Fig. 1A). A rapid urease test was positive for H. pylori. Histologic sections of the high and low bodies showed patchy infiltration of small lymphocytes into the lamina propria and lymphoepithelial lesions; the lymphocytes were focally aggressive toward the gland (Fig. 1B). Phenotypic analysis showed that the lesion was positive for CD20, but negative for CD3, CD5, CD10, and Bcl-6, and that its proliferation rate was <2%, as shown by MIB1 (Ki-67) antibody analysis. Based on these histopathological and phenotypic features, the patient was diagnosed with low-grade MALT lymphoma. Staging procedures were performed. Endoscopic ultrasound (EUS) revealed hypoechoic disruption of the mucosal and submucosal layers; moreover, the fourth layer was preserved and there was no evidence of locoregional lymphadenopathy (u-T1smN0) (Fig. 1C). A computed tomography (CT) scan showed a huge LN, about 30×15 mm in size, in the subcarinal area (Fig. 1D). Fusion whole body positron emission tomography (PET) showed a hypermetabolic lesion, suggestive of a malignant lesion, on the subcarinal area. (Fig. 1E). Bone marrow biopsy findings were normal. EUS of the subcarinal lesion showed 32×12 mm LN. Histopathological and phenotypic analysis of a biopsy sample obtained by EUS-guided fine needle aspiration (Fig. 1F) showed that the lesion was a MALT lymphoma (Fig. 1G). The patient was diagnosed with a stage 4E gastric MALT lymphoma. For H. pylori eradication, the patient was treated with a 14-day course of amoxicillin 2,000 mg a day, clarithromycin 1,000 mg a day and pantoprazole 80 mg a day.
Fig. 1
Fig. 1
Initial diagnostic tests. (A) Initial upper gastrointestinal endoscopy displaying a shallow ulcerative lesion in the gastric high body and a hyperemic lesion in the gastric low body. (B) Histopathologic examination of a gastric biopsy specimen displaying (more ...)
An endoscopy performed 2 months after treatment showed that the gastric high and low bodies were pale and flat, with no evidence of lymphoma infiltration (Fig. 2A and C). EUS of the subcarinal area and CT showed that the LN had decreased markedly in size, to 12×11 mm (Fig. 2E and G). Follow-up PET showed no significantly abnormal hypermetabolic lesions (Fig. 2I).
Fig. 2
Fig. 2
Follow-up evaluations 2 months (A, C, E, G, I) and 1 year (B, D, F, H, J) after Helicobacter pylori eradication. (A, C) Upper gastrointestinal endoscopy, displaying pale, flat gastric high and low bodies without lymphoma infiltration (H&E stain, (more ...)
One year after treatment, all assessments, including endoscopy with biopsy, CT, PET, and EUS, showed normal results (Fig. 2B, D, F, H and J). At present, 14 months later, the patient remains in complete remission.
More than 90% of gastric lymphomas are related to the presence of H. pylori; hence, eradication of H. pylori is the favored initial treatment for patients with early-stage H. pylori-positive gastric MALT lymphoma.2
However, the association between extragastric MALT lymphoma and H. pylori is not clear. Although several case reports have described the regression of extragastric MALT lymphomas after H. pylori eradication,3,4 one study showed that the majority of patients with extragastric MALT lymphoma did not benefit from H. pylori eradication.5
In addition, there have been a few case reports showing that H. pylori eradication has led to the regression of advanced gastric MALT lymphomas simultaneously involving two or more organs other than the stomach.6,7 Recirculation of H. pylori - specific T-cells from the stomach to other organs via the blood or lymphatic system may trigger an inflammatory response in other MALT-lymphoma containing organs.3,4,6,7 Alternatively, abnormal cells may spread from the stomach to other organs via the blood or lymphatic system.5,8
H. pylori eradication may also lead to the regression of secondarily involved perigastric LN and bone marrow. However, our patient was different, in that H. pylori eradication led to the regression of a mediastinal LN.
The treatment for advanced gastric MALT lymphoma has not been clearly defined. Treatment is usually similar to that for patients with other advanced-stage indolent non-Hodgkin lymphoma.9 Our findings, however, indicate that H. pylori eradication should be the first treatment in patients presenting with H. pylori-associated advanced gastric MALT lymphoma. Further molecular characterization of these tumors is necessary to determine the most suitable therapeutic strategy.
Footnotes
No potential conflict of interest relevant to this article was reported.
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Articles from Gut and Liver are provided here courtesy of
The Korean Society of Gastroenterology, the Korean Society of Gastrointestinal Endoscopy, the Korean Society of Neurogastroenterology and Motility, Korean College of Helicobacter and Upper Gastrointestinal Research, Korean Association for the Study of Intestinal Diseases, the Korean Association for the Study of the Liver, the Korean Society of Pancreatobiliary Disease, and the Korean Society of Gastrointestinal Cancer