What role does Helicobacter pylori eradication play in gastric MALT and gastric MALT lymphoma?

被引:86
作者
Thiede, C
Morgner, A
Alpen, B
Wundisch, T
Herrmann, J
Ritter, M
Ehninger, G
Stolte, M
Bayerdorffer, E
Neubauer, A
机构
[1] TECH UNIV DRESDEN, MED KLIN 1, D-01307 DRESDEN, GERMANY
[2] UNIV MAGDEBURG, KLIN INNERE MED GASTROENTEROL HEPATOL & INFEKTIOL, D-39106 MAGDEBURG, GERMANY
[3] INST PATHOL, BAYREUTH, GERMANY
关键词
D O I
10.1016/S0016-5085(97)80014-5
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The concept of mucosa-associated lymphoid tissue (MALT) has been introduced to differentiate biological functions from behavior of nonnodal vs. nodal lymphoid tissues. Lymphomas arising from MALT also behave differently than typical nodal lymphomas. In contrast to other tissues, MALT in the stomach is almost exclusively a result of Helicobacter pylori infection. Thus, MALT is part of the host defense against the pathogen H. pylori. Consequently, lymphomas arising from gastric MALT may be a clonal evolution starting from the infection. In low-grade gastric MALT lymphoma, cure of the infection may induce complete histological remission in the majority of patients. Investigators have recently reported that complete remission rate is between 70% and 80%. In an extended analysis, we have treated 84 patients with low-grade gastric MALT lymphoma in stage EI, using a dual regimen to eradicate H. pylori. Complete remission was observed in 68 (80%) patients; a partial remission was found in 4 patients. In contrast, 12 patients showed no change and were referred to alternative treatment. In patients in complete remission, a polymerase chain reaction assay for the rearranged immunoglobulin heavy-chain gene remained positive in many cases. Together with data from the literature, these data suggest that the majority of patients with low-grade gastric MALT lymphomas in stage El--- respond to eradication of H. pylori. Longer follow-up investigations are necessary to determine if remissions indicate a cure from the disease.
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页码:S61 / S64
页数:4
相关论文
共 18 条
[1]   REGRESSION OF PRIMARY GASTRIC LYMPHOMA OF MUCOSA-ASSOCIATED LYMPHOID-TISSUE TYPE AFTER CURE OF HELICOBACTER-PYLORI INFECTION [J].
BAYERDORFFER, E ;
NEUBAUER, A ;
RUDOLPH, B ;
THIEDE, C ;
LEHN, N ;
EIDT, S ;
STOLTE, M .
LANCET, 1995, 345 (8965) :1591-1594
[2]   ROLE OF HELICOBACTER-PYLORI ERADICATION IN HIGH-GRADE MALT LYMPHOMA [J].
BOOT, H ;
DEJONG, D ;
VANHEERDE, P ;
TAAL, B .
LANCET, 1995, 346 (8972) :448-449
[3]   PREVALENCE OF LYMPHOID FOLLICLES AND AGGREGATES IN HELICOBACTER-PYLORI GASTRITIS IN ANTRAL AND BODY MUCOSA [J].
EIDT, S ;
STOLTE, M .
JOURNAL OF CLINICAL PATHOLOGY, 1993, 46 (09) :832-835
[4]  
FISCHBACH W, 1996, GASTROENTEROLOGY, V110, pA512
[5]   MALIGNANT-LYMPHOMA OF MUCOSA-ASSOCIATED LYMPHOID-TISSUE [J].
ISAACSON, PG ;
SPENCER, J .
HISTOPATHOLOGY, 1987, 11 (05) :445-462
[6]   Cure of Helicobacter pylori infection and duration of remission of low-grade gastric mucosa-associated lymphoid tissue lymphoma [J].
Neubauer, A ;
Thiede, C ;
Morgner, A ;
Alpen, B ;
Ritter, M ;
Neubauer, B ;
Wundisch, T ;
Ehninger, G ;
Stolte, M ;
Bayerdorffer, E .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (18) :1350-1355
[7]   ERADICATION OF HELICOBACTER-PYLORI INFECTION IN PRIMARY LOW-GRADE GASTRIC LYMPHOMA OF MUCOSA-ASSOCIATED LYMPHOID-TISSUE [J].
ROGGERO, E ;
ZUCCA, E ;
PINOTTI, G ;
PASCARELLA, A ;
CAPELLA, C ;
SAVIO, A ;
PEDRINIS, E ;
PATERLINI, A ;
VENCO, A ;
CAVALLI, F .
ANNALS OF INTERNAL MEDICINE, 1995, 122 (10) :767-769
[8]   Gastric mucosa-associated lymphoid tissue lymphomas: More than a fascinating model [J].
Roggero, E ;
Zucca, E ;
Cavalli, F .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (18) :1328-1330
[9]  
RUDOLPH B, 1997, J CLIN ONCOL, V15, P114
[10]   Regression of gastric MALT lymphoma after eradication of Helicobacter pylori is predicted by endosonographic staging [J].
Sackmann, M ;
Morgner, A ;
Rudolph, B ;
Neubauer, A ;
Thiede, C ;
Schulz, H ;
Kraemer, W ;
Boersch, G ;
Rohde, P ;
Seifert, E ;
Stolte, M ;
Bayerdoerffer, E ;
Allmendinger, D ;
Baestlein, E ;
Baghdadi, F ;
Berges, W ;
Bode, J ;
Chalybaeus, C ;
Diehl, HG ;
Frevel, M ;
Gieseler, U ;
Habbig, J ;
Heidegger, AE ;
Hotz, J ;
Huelskath, H ;
Itzen, WH ;
Judmaier, G ;
Kolthoff, H ;
Krautter, H ;
Kuehner, W ;
Manegold, CE ;
Pechlivanis, C ;
Puerner, K ;
Schloemann, L ;
Schmitz, L ;
Schmitz, R ;
Stadelmann, O ;
Stein, H ;
Stoian, L ;
Stumpf, J ;
Thilo, A ;
Trump, F ;
Wambach, G ;
Weismueller, J ;
Zellman, A .
GASTROENTEROLOGY, 1997, 113 (04) :1087-1090